- Open Access
Targeting PDZ domains as potential treatment for viral infections, neurodegeneration and cancer
Biology Direct volume 16, Article number: 15 (2021)
The interaction between proteins is a fundamental event for cellular life that is generally mediated by specialized protein domains or modules. PDZ domains are the largest class of protein–protein interaction modules, involved in several cellular pathways such as signal transduction, cell–cell junctions, cell polarity and adhesion, and protein trafficking. Because of that, dysregulation of PDZ domain function often causes the onset of pathologies, thus making this family of domains an interesting pharmaceutical target. In this review article we provide an overview of the structural and functional features of PDZ domains and their involvement in the cellular and molecular pathways at the basis of different human pathologies. We also discuss some of the strategies that have been developed with the final goal to hijack or inhibit the interaction of PDZ domains with their ligands. Because of the generally low binding selectivity of PDZ domain and the scarce efficiency of small molecules in inhibiting PDZ binding, this task resulted particularly difficult to pursue and still demands increasing experimental efforts in order to become completely feasible and successful in vivo.
Proteins take part in almost all biological processes, and exert their functions in different ways, ranging from enzyme catalysis to mediating the recognition of other molecules, such as small ligands, or binding nucleic acids or other proteins. Protein–protein interactions (PPIs) represent a key event for several physiological cellular pathways of living organisms including gene expression, cell growth, proliferation, nutrient uptake, metabolism, morphology, motility, intercellular communication and apoptosis.
PPIs are mediated by structural domains with the function to recognize and bind specific sequences on other proteins. These interaction domains are grouped into families and classes, based on structural features, sequence homology and the ability to recognize and interact with specific motifs and sequences [1, 2]. For example, phosphotyrosine containing motifs are mainly recognized by SH2 and PTB domains [3,4,5], while phosphoserine/threonine containing sequences by 14-3-3 proteins, FHA domains, WW domains and WD40 domains . Acetylated or methylated lysine residues are specifically recognized by Bromo and Chromo domains, respectively [7,8,9]. Other domains that do not bind post-translationally modified sequences, recognize peptide motifs carrying other features. For instance, SH3, WW, EWH1 domains recognize proline-rich sequences [10,11,12]. Furthermore, other interaction domains so far known mediate specific cellular physiological functions, such as apoptosis (DD, DED, CARD, BH 1-4 domains) [13,14,15,16], vesicle trafficking (GYF, Snare, VHS domains) [17,18,19] and dimerization (SAM domain) .
Among PPIs modules, PDZ domains are the largest class in the human proteome, with around 274 PDZ domains identified in 155 proteins . PDZ domains are often present in multidomain scaffold and anchoring proteins, involved in the formation of transient complexes that support several cellular processes such as protein trafficking, signal transduction, cell–cell junctions, and cell polarity and adhesion. Hence, due to their relevant physiological role, whether interactions mediated by PDZ domains are dysregulated, a pathological state often occurs in the cell.
Given these premises, the modulation and inhibition of PDZ domains-mediated protein interactions are attractive targets in the field of drug discovery. Overall, the knowledge about different PPIs and domains involved in protein interaction is essential not only to understand molecular mechanisms at the basis of the cellular processes, but it is also important to clarify the development of disease states in which PPIs are implicated. Noteworthy, different strategies are applied to develop inhibitors directed against certain PPIs whose function can be altered in certain pathological conditions. In this review work, we recapitulate the implication of PDZ domains in diseases such as cancer, cystic fibrosis, neurological disorders and viral infections. In particular, the attention will be focused on those PDZ domains identified as potential therapeutic targets and on the strategies conceived to hijack their dysregulated interactions.
PDZ domains structure and function
PDZ domains are small protein modules containing approximately 80–110 amino acids folded in a compact tertiary arrangement, typically consisting of six antiparallel β-strands and two α-helices, with few exceptions. They take their name from Postsynaptic density-95, Disks-large and Zonula occludens-1 proteins, in which they were identified for the first time in the early 1990s [22,23,24]. Usually, PDZ domains bind the C-terminal sequence of their cognate partners. Ligand binding occurs in a groove formed by the α2 helix and the β2 strand, and the chain of the C-terminal residue of the ligand engages into a hydrophobic pocket on the surface of the domain [25, 26] (as shown in Fig. 1). The binding groove is characterized by the presence of a highly conserved lysine or arginine residue that interacts with the carboxylate group at the end of the peptide. In addition to this electrostatic interaction, three main-chain amide protons of the Gly-Leu-Gly-Phe motif form hydrogen bonds with the C-terminal region of the peptide leading to the more general binding signature R/K-XXX-GLGF.
Conventionally, the C-terminal amino acid of the ligand is numbered as position 0 and the rest of the residues are named in reverse order as position -1, -2, -3 etc. Based on the PDZ binding motif (PBM) of the ligand, three major binding classes have been identified, although lately it has been further expanded into a total of 16. Even if PDZ domains recognize more than 5 residues upstream of the C-terminal residue, the P0 and P-2 positions are particularly significant for specificity. Position 0 is frequently a hydrophobic residue, according to differences in shape and size of the PDZ binding pocket, as in the case of PDZ1 and the PDZ2 of PSD-95, able to recognize sequences ending with valine, leucine and isoleucine [25, 27]. Position -2 is crucial for binding specificity and determines the basis of the entire classification. Class I is characterized by the presence of a serine or a threonine at position -2, with the formation of a hydrogen bond with the N3 of an histidine residue which is highly conserved in the PDZ α2 helix. Class II presents hydrophobic residues at the position -2. Class III recognizes a tyrosine in the PDZ binding groove, establishing a hydrogen bond with the aspartate carboxylic group of the ligand. PBMs can also occur in internal sequences, and membrane phospholipids can be recognized by PDZ domains [28, 29]. As for example, neuronal nitric oxide synthase (nNOS) and the PDZ domain of syntrophin  interact through a nonterminal hairpin turn of nNOS in an unusual head-to-tail arrangement.
Role of PDZ-containing proteins in human diseases
PPIs mediated by PDZ domains have a critical role in the regulation of a broad variety of biological processes. PDZ domains are crucial in the assembly of the molecular machinery of different transduction pathways being often found in multidomain scaffold proteins implicated in the regulation of pre- and post-synaptic signalling in neuronal cells, maintenance of cell–cell junction communication and ion-channel trafficking regulation. Dysregulation of such processes is at the basis of several disorders and diseases highlighting PDZ domains as promising drug targets.
PDZ domains are present in proteins involved in formation of cellular polarity and signalling complexes as well as in the binding to receptors and in localization of channels and enzymes. Thereby they are mainly located at level of the cellular membranes and cytoskeleton and play a central role in processes requiring cell–cell or protein–protein contacts , thus orchestrating para- and intra-cellular pathways. As a consequence, dysfunctional PDZ-containing proteins influence development and progression of cancer diseases by determining loss of cell polarity, cell–cell contacts signaling pathways and controlling proliferation, differentiation and apoptosis [32, 33]. Several tumours such as breast, cervical, colon, prostate, liver cancers and glioblastoma often see the involvement of PDZ domains .
PDZ domains involved in cell polarity
Cell polarity is a key feature of specialized cells, finely regulated and tuned, both spatially and temporarily, by several PDZ-containing proteins. In general, it relies on the asymmetric distribution of macromolecules, like proteins, lipids and RNA of the plasma membranes of epithelial and endothelial cells and neurons, pinpointing defined regions (namely basal, apical, basolateral) with specific structural and functional features .
Cell polarity and communications between adjacent cells are ensured by specific structures named adherent junctions (AJs) and tight junctions (TJs). AJs are prevalently found at the basolateral region and regulate cell–cell adhesion through transmembrane proteins named nectins and cadherins. Tight junctions (TJs) determine the membrane polarity by the action of membrane proteins named occludin and claudin , localizing components across the different sides of the membranes and regulating ions and solutes transport among cells. TJs and AJs play a key role in the maintenance of tissue integrity and regulate essential cellular functions, such as proliferation, apoptosis, metabolism, differentiation, and motility.
The link between cell polarity and tumor proliferation processes has been identified for the first time in Drosophila . Most polarity complexes forming TJs and AJs are composed by several PDZ-containing proteins: (i) PAR (partitioning-defective) complex generating TJs are formed by interaction between Par3 and Par6 with the atypical protein kinase C (aPKC) and cell division control protein (CDC42); (ii) CRUMBS polarity complex is composed by the transmembrane protein CRUMBS and the scaffolding PDZ-containing proteins PALS1 e PATJ; (iii) SCRIBBLE complex generating AJs are composed of e-cadherin and Scrib, interacting with DISCS large proteins (Dlg) and Lethal-2-giant larvae proteins (Lgl) . Furthermore, the AJs and TJs are physically linked by the zonula occludens proteins (ZO), and include other PDZ domain-containing proteins as signaling molecules and actin cytoskeletal modifiers . Several of these PDZ proteins belong to the MAGUK family, scaffolding proteins recruiting cellular receptors and signaling molecules.
Since AJ and TJ are distinctive of specialized differentiated cells, disturbances of these complexes were found to be strongly correlated to cancer . In particular, loss of tissue integrity and subsequent increased tendency to invasion and metastasis of cancer cells  have been ascribed to dysfunction of Scrib , Magi [40, 41], Dlg-5 [42, 43], Patj, Lin7, Par3 and Par6 , ZO1 , ZO2 [34, 46, 47], and Dlg1 . The latter, being part of the Scribble polarity complex, leads to uncontrolled epithelial cell proliferation and neoplastic transformation.
PDZ domains mediate signalling complexes formation
The role played by PDZ domains in recruiting proteins involved in molecular signal transduction complexes implied in cell survival, apoptosis, proliferation and differentiation makes them important pharmacological targets in cancer. The oncosuppressor Pten is able to bind the PDZ domains of the Par3, NHERF and Magi-1 proteins. In particular, the binding of Magi-1 to Pten protects it from degradation [40, 49, 50], down-regulates of the PI3K/Akt pathway  and exerts an oncosuppressor activity. Interestingly, in acute lymphoblastic leukemia  and in colon cancer the expression of Magi-1 is commonly found downregulated.
Another important example is represented by the PDZ-containing protein Syntenin, also named melanoma differentiation-associated gene-9 (MDA-9). Syntenin expression is increased in metastatic and invasive cells [53, 54]. Numerous studies have shown that syntenin is involved in the formation of metastasis, cell migration and cytoskeletal rearrangement through the activation of the nuclear factor-kappa B (NF-kB) pathway (Fig. 2) [55, 56] which regulates the expression of genes involved in cell motility and invasion . From a structural perspective, Syntenin comprises a tandem of two PDZ domains mediating its activity. Liu and coauthors designed a dimeric ligand binding both PDZ1 and PDZ2 domains with high affinity , preventing the interaction with cellular targets. The dimeric inhibitor is based on two sequences naturally interacting with Sytentin PDZ domains, connected each other through a PEG3 (triethylene glycol) linker and modified at positions -2 and -1 with the amino acid naphthyl-alanine. In vitro experiments conducted by Liu and co-workers reported high affinity (KD = 0.21 ± 0.01 µM), together with the ability to reduce cellular migration by downregulating ERK/MAPK pathway in cellula (58).
A recent work by Haugaard-Kedström and co-workers reported the design of new monomeric peptides (KLS-128018, KSL-128114) able to bind PDZ1 of Syntenin in a non-canonical way with high affinity. These Peptides showed a promising effect against highly aggressive cancer forms, such as glioblastoma (GBM) .
PDZ domains bind G protein coupled receptors
G protein coupled receptors (GPCR) are a family of receptors that regulate numerous physiological functions. Several GPCRs are reported as binders of PDZ domains through their PDZ binding motifs (PBMs) . Since the main pathways triggered by GPCRs, PKA and PLC signaling pathways, regulate cell survival, growth, migration and differentiation [61, 62], alterations of the binding between PDZs and GPCRs are often tumorigenic.
A typical example is represented by the Frizzled receptor (Frz). It is involved in the activation of the Wnt signal pathway through the interaction of its C-terminal PBM with the PDZ-containing protein Disheveled (Dvl) . Dvl triggers the activation of two signaling pathways: the canonical pathway activating the β-catenin dependent cell proliferation  and the non-canonical pathway regulating cytoskeletal remodeling and cell migration . Both pathways are involved in tumorigenesis [66, 67]. Given the importance of this signalling pathway in the onset of cancer, targeting the PDZ domain of Dvl protein represents a promising antitumor strategy, especially by inhibiting the interaction with Frizzled proteins.
In particular, Frizzled 7 (Frz7) is a receptor subtype highly expressed in a broad range of tumours, exerting its oncogenic activity through Wnt pathway activation. The disruption of this interaction can be selectively addressed by designing inhibitors with peculiar characteristics. Fujii and coworkers  proposed a small molecule, called FJ9, which was reported to inhibit the binding between Frz7 and the PDZ domain of Dvl. This inhibition lowered cytosolic level of β-catenin in a dose-dependent manner, downregulating the canonical Wnt pathway in cells and inducing apoptosis in human lung cancer and melanoma cells.
In another work from Mahindroo et al.  a small molecule was successfully designed to disrupt the interaction between Frz7 and PDZ of Dvl. The molecule, an indole-2-amide compound, was able to bind the PDZ domain by mimicking the side chains of the second and fourth amino acid residues of the endogenous ligand through the substituents at positions 2 and 3 of the indole. The compound was found to interact with Frz7 and exert an apoptotic effect by down-regulating Dvl-driven Tcf activation of transcription.
Zhang and coauthors have elegantly designed, through phage-display, short peptides mimicking internal ligands binding the isoform 2 of Dvl (Dvl2) able to inhibit the Wnt/β-catenin pathway. Among these peptides (called pepN1, pepN2 and pepN3), pepN3 inhibited the Wnt/b-catenin pathway in a dose-dependent manner with potency (IC50 of 11 ± 4 µM) superior to FJ9 (see above in the paragraph) and was atoxic for the cells at active concentrations .
Several other proteins, such as LARG-Rho , CAR11 , GIPC1 , NHERF1-2 , PREX1 , TIAM1 , show interaction with GPCRs and are associated to cancer, an aspect reinforcing the view that targeting PDZ mediated protein–protein interactions may be a powerful strategy aimed to develop effective antitumor pharmacological strategies.
Cystic fibrosis is a genetic disorder caused by mutations in the CFTR gene encoding Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). CFTR protein is a chloride channel activated by local cAMP that is located in the apical membrane of epithelial cells. The activity of CFTR contributes to maintaining the correct state of hydration on the epithelial surface by regulating the flux of ions and fluid through the plasma membrane [75,76,77]. CFTR is expressed in different organs including lung, intestine, pancreas and kidney. Given its important physiological role, dysregulation of CFTR signaling causes severe defects in these organs. The impairment in the transport of ions through the epithelial membrane leads to an accumulation of thick mucus in the lung that obstructs the airways [78,79,80].
Several PDZ proteins are involved in the regulation of CFTR. In particular, CAL (CFTR associated ligand) has been identified as an important regulator of CFTR endocytic trafficking and lysosomal degradation . CAL is a protein of 461 residues that is ubiquitously expressed. Its structure consists of unstructured (unfolded) N- and C-terminal regions, a coiled-coil domain and a PDZ domain (Fig. 3). The PDZ domain of CAL contains a His residue at the N-terminal of α2 helix which allows it to bind preferentially PBMs of class I. The recognition of a PBM in CFTR and the PDZ domain of CAL promotes the degradation of CFTR in lysosomes, with consequent reduction of the levels of CFTR on the plasma membrane surface [82,83,84]. Other two PDZ-domain proteins, the two isoforms of Na+/H+ exchanger regulatory factor (NHERF 1 and 2), have been identified as positive regulators of CFTR. NHERF 1 and NHERF 2 recognize the cytoplasmic tail of CFTR through their two PDZ domains, stabilizing its localization at the plasma membrane and thus regulating its activity .
The most common mutation occurring on CFTR gene and causing CF is the deletion of the Phe508 residue (∆F508) . This mutation causes an inefficient folding of the protein and a decreased channel activity, as well as a rapid degradation mediated by the interaction between CFTR PBM and the PDZ domain of CAL [82, 86, 87]. Examples of molecules identified as inhibitors of PDZ-domain mediated interactions involved in the cystic fibrosis will be discussed.
Inhibitors of PDZ-domains mediated interactions for the treatment of cystic fibrosis
Small molecules have been designed to induce correct folding and channel activity of ∆F508 CFTR [88, 89]. However, due to the rapid degradation in the cell of the protein mediated by CAL, this approach could be applied only in in vitro experiments. In a different work , by knocking down CAL in a bronchial epithelial cell line derived from a CF patient ∆F508, CFTR expression and channel activity has been restored. This result suggested that the inhibition of the interaction between the PDZ domain of CAL and CFTR could represent a potential treatment for cystic fibrosis.
Since both CAL and NHERF proteins recognize CFTR, a specific inhibitor of CAL PDZ – CFTR interaction was designed . Through a combination of library screening and different steps of optimization, a decameric peptidyl inhibitor called iCAL3610 was produced (Fig. 3). This molecule showed high affinity for CAL PDZ (Ki = 17.3 ± 4.3 µM) and low affinity for the PDZ-domains of NHERF proteins (Ki > 5000 µM for the PDZ1 and PDZ2 of NHERF1; Ki > 5000 µM and Ki > 3000 µM for PDZ1 and PDZ2 of NHERF2, respectively). Experiments conducted in airway epithelial cell lines from CF patients demonstrated that iCAL3610 was able to increase the half-time of CFTR at the plasma membrane and to enhance the activity of the channel .
The use of peptides targeting the PDZ domain of CAL to inhibit its interaction with CFTR resulted as an effective strategy, with some limitations due to low cell-permeability and metabolic stability. In a recent study  a peptide called PGD97 was designed to overcome these difficulties. It presents two distinctive regions, a cell-penetrating peptide (CPP) and a binding sequence for CAL PDZ, which forms as a disulfide-cyclized macrocycle and becomes linear in the intracellular environment. In cellula experiments demonstrated that PGD97 is able to stabilize ∆F508 CFTR and improve CFTR functions , representing a potential novel treatment for cystic fibrosis.
Nervous system disorders
Neuronal network is finely regulated during synaptic transmission. In the synapses, neurotransmitter transporters and receptor complexes are localized in the presynaptic and postsynaptic region respectively, and a fine regulated control is necessary to guarantee the correct propagation of the signal . Abnormal synaptic transmissions are at the origin of a plethora of different pathological conditions. In this scenario, receptor complexes represent the site of action of almost 40% approved drugs, highlighting the importance of these proteins as pharmacological targets [95, 96].
Among the others, PDZ-containing proteins are particularly important for the formation, function and localization of postsynaptic receptor complexes [97, 98]. PDZ proteins can interact not only with membrane proteins but also with cytoplasmic proteins producing a large variety of signalling complexes [99, 100]. Remarkably, PDZ-containing proteins are also involved in the regulation of synaptic adhesion and maturation of excitatory synapses, as exemplified by the case of PSD-95 [97, 101, 102]. Their abundance and crucial role in the regulation of different neurological processes, establish a close link between PDZ dysfunction and the onset of different pathological conditions. In this paragraph we will focus our attention on the role of PDZ domains in the onset of different neurological pathologies .
Autism spectrum disorder (ASD)
ASD is a neurodevelopmental condition that affects childhood population on average 1 in 68 . Autistic patients are characterized by behavioural abnormalities such as reduced vocal communication, aberrant social interactions and repetition [104, 105], caused mainly by impairments in synaptic plasticity and synaptic processing.
Synaptic plasticity is mainly controlled at the level of the postsynaptic density (PSD) region . PSD-95 is one of the major components of PSD and it is composed of three N-terminal PDZ domains and an SH3-GK module [107,108,109]. It is able to interact, through its PDZ domains, with NMDA receptor subunits, NR2A and NR2B, and with AMPA receptor accessory proteins , and it plays a key role in regulating plasticity of glutamatergic synapses (schematized in Fig. 4) during neurodevelopment . As a prevalent component of the postsynaptic density region, the disruption of PSD-95 physiological interactions has been correlated with the onset of ASD [105, 110,111,112].
Additional evidence of aberrant interactions between PSD-95 and PDZ-containing SHANK family proteins corroborates the link between PSD-95 and ASD [105, 113]. SHANK proteins are scaffolding proteins involved in the formation of large complexes crucial for synaptic development and function. An increasing amount of data indicate that mutations in the genes that encode for SHANK proteins may be correlated with several behavioural abnormalities in mice models, some of which are considered ASD-like behaviours [113,114,115,116,117,118]. This evidence points the attention on PDZ-containing proteins as targets to develop pharmacological strategies against ASD.
Alzheimer’s disease (AD)
AD is a neurodegenerative condition that is becoming dramatically relevant in terms of health care and welfare in the modern world [119, 120]. A peculiar characteristic of AD is the accumulation of protein aggregates (or plaques) in the brain tissue [120,121,122]. Principal components of AD plaques are the Amyloid beta (Aβ) peptides, natural products of amyloid precursor protein (APP) metabolism . APP is a transmembrane protein of 695–770 amino acids, cleaved by the action of β- and γ-secretases that generate Aβ fragments of various lengths. The Aβ1-42 variant displays a high propensity to form insoluble aggregates.
One of the major interactors of APP is Munc18-interacting proteins (Mints or X11s) [123,124,125]. Mint proteins present a variable N-terminal region, and a conserved C-terminal region that contains a phosphotyrosine binding (PTB) domain and two PDZ domains. Interestingly, PDZ domains of Mint are regulated by an intramolecular mechanism, in which the highly conserved C-terminal tail of Mint is able to inhibit the binding of the construct . The PTB domain binds the conserved YENPTY motif of APP controlling its trafficking and regulating Aβ fragments production [127, 128]. Additional evidence about the involvement of Mint in the onset of AD derives from the description of the interaction between its PDZ domains and Presenilin-1 [129,130,131], the catalytic subunit of the γ-secretase complex. The interaction between the PDZ domains of Mint with Presenilin-1 promotes APP/Presenilin-1 colocalization regulating Aβ fragments formation. Altogether, these findings indicate that APP/Mint/Presilin-1 interaction is of great interest for potential treatment of AD, with PDZ modulation as a feasible therapeutic target.
Parkinson's disease (PD)
PD is a neurodegenerative disorder affecting 2–3% of the population over 65 years old. PD is the most common neurodegenerative movement disease, characterized by a loss of dopaminergic neurons in the substantia nigra and the accumulation of protein aggregates called Lewy bodies [132, 133]. The main constituent of Lewy bodies is α-synuclein protein, which tends to form aggregate as a consequence of misfolding [120, 134].
The molecular mechanism of α-synuclein misfolding has been extensively investigated, but still poorly understood. One of the prevalent causes of protein misfolding is the exposure of cells to internal and external stress which cells tend to contrast through different strategies. An example is represented by the oligomeric HtrA protease family . HtrA protease contains one or two C-terminal PDZ domains, which bind misfolded proteins, triggering the activation of the trypsin-like protease domain for degradation [135,136,137]. A direct correlation between the mammalian HtrA2 inactivation and the onset of PD has been established in different studies [138,139,140], and PD patients have been identified through missense mutations in the gene encoding for HtrA [138, 139]. Interestingly, one of these mutations, p.G399S, affects one of the PDZ domains of HtrA2 . Other studies performed on HtrA2 deficient mice exhibiting neurodegeneration and a parkisonian phenotype [140, 141] report additional evidence of the correlation between HtrA2 inactivation and the onset of PD.
Hearing and vision diseases
Hearing and vision mechanisms control is mainly achieved by clustering signaling proteins in large molecular complexes, the organization of which foresees the action of many PDZ-containing proteins.
Usher syndrome (USH) is a syndrome affecting hearing, vision and body balance, and represents the most common form of hearing and vision loss . PDZ domains play a pivotal role in the onset of this pathology. Two pioneering works by Verpy and colleagues and Bitner-Glindzicz and colleagues described mutations in a gene encoding the PDZ-containing protein Harmonin  that lead to Usher type 1C (USH1C) disease .
Usher syndrome can occur in three distinct forms with USH type 2 (USH2) as the most common. Among the others there are three genes that are recognized to cause USH2 named USH2A, GPR98, and WHRN, whereas a fourth gene, PDZD7, is a modifier gene found in USH2 patients [145, 146]. Two of these genes, WHRN and PDZD7, codify for PDZ-containing proteins able to mediate the formation of a quaternary complex with the other two proteins codified by USH2A and GPR98 . Inactivation and mutations in the PDZ domains of Whirlin and PDZD7 proteins have been associated directly to the manifestation of USH2 [143, 145, 147].
Ischemic stroke represents the leading cause of disability and the second cause of death worldwide, with an urgent need for pharmacological therapies able to relieve neuronal damages . The interaction between the PDZ domains of PSD-95 and the N-methyl-D-aspartate (NMDA) receptor is a key step in the onset of stroke. In particular, this interaction causes an overproduction of nitric oxide and consequent neuronal death . On these bases, a suitable candidate for the treatment of neuronal damage after stroke is represented by hijacking the interaction between the PDZ domains of PSD-95 and NMDA.
Targeting PDZ domains as potential neurological treatment
PDZ domains represent an extremely interesting candidate for novel neurological treatments. A peculiar feature of PDZ domains is their presence as tandem repeats [150,151,152]. Interfering with multiple PDZ domains simultaneously can enhance both affinity and selectivity of a putative inhibitor and the design of multivalent ligands to target protein–protein interactions is a promising strategy for the treatment of neurological disorders.
An important example is NA-1 (now in phase 3 of the clinical trial NCT04462536) which targets PDZ domains of MAGUK family proteins (PSD-95, PSD-93, SAP-97 and SAP-102) . The MAGUK structural architecture is generally composed by a tandem repeat of PDZ domains followed by a SH3 and a GK domain. MAGUK proteins are responsible for the formation of post-synaptic protein complexes and are potential drug targets for the treatment of different neurological pathologies. Since the interaction between PSD-95 and N-methyl-D-aspartate receptor (NMDA) and neuronal NO synthase (nNOS) is mediated by PSD-95 PDZ domains, Nissen et al. designed and produced a trimeric ligand able to bind simultaneously PDZ1-2–3 domains of PSD-95. NA-1 showed high binding affinity towards these MAGUK proteins, confirming the therapeutic importance of this PDZ-protein interaction.
Another example of a potential treatment of dysfunctional neurological conditions obtained by inhibiting PDZ domain-mediated interaction is the Tat-P4-(C5)2 peptide, studied in vivo by Christensen and coworkers . To avoid direct targeting and inhibition of NMDA and AMPA receptors, which could lead to significant side effects, a peptide with the ability to interfere with synaptic PDZ domain-scaffold protein PICK1 was developed. PICK1 regulates the expression and activity of AMPA receptors and mediates important membrane protein interactions, including those with the GluA2 subunit of AMPA. Tat-P4-(C5)2 resulted in being able to block two different regions of the PICK1 PDZ domain, leading to the disruption of the interaction with AMPARs, and consequently, limiting the dysfunctional synaptic plasticity associated with correlated neurological disorders, such as neuropathic pain.
Viral proteins targeting PDZ domains
A large number of PDZ-containing proteins possess a fundamental role in maintaining the correct physiology of the cell and in determining key aspects of specialized cells, as for example cell polarity in epithelial and neuronal cells. Under this light, it is not surprising that several viral pathogens have evolved PDZ-binding motifs in their proteins to target host cell PDZ domains and disrupt physiological interactions to favor viral replication and disease progression.
At the end of 1990s, the first PBMs in viral proteins were identified in HTLV-1 Tax protein , high-risk HPV E6 oncoproteins , and adenovirus E4 oncoprotein . Since then, many other viral proteins were found to present PBMs in their sequence and the evolutionary strategy of viral pathogens to target these protein–protein interactions became clearer. In fact, a wide range of pathologies may arise from viruses that developed the ability to target PDZ protein functions and many well-established PDZ targeting viral proteins have been pinpointed and characterized [155, 158,159,160,161,162,163] reinforcing the evidence on how PDZ domains represent fundamental pharmacological targets in the struggle to prevent and cure several viral diseases.
PBM of Coronaviruses Envelope protein
A typical example of viral protein targeting PDZ domains upon infection is represented by coronaviruses MERS-CoV, SARS-CoV, and SARS-CoV-2 Envelope (E) membrane proteins. The genome of coronaviruses typically encodes for four major structural proteins, including spike (S), nucleocapsid (N), membrane (M), and envelope (E) proteins. The E protein is a tiny integral membrane protein that is poorly present in the mature virus, while being highly expressed in the host cell, where it forms, through interaction of their transmembrane domain, pentameric ion channels mainly involved in virion maturation and trafficking .
E proteins from SARS-CoV and SARS-CoV-2 possess a PBM at their C-terminus which allows them to interact with PDZ-containing proteins in the host cell. Their primary structures have 98% sequence identity. The few variations appreciable between the two protein sequences occur at their C-terminal domain and do not affect the PBM. Although the exact role of these interactions is not well established, there is evidence about SARS-CoV E protein PBM as virulence factor . In cellula experiments reported that the removal of the PBM from SARS-CoV E protein resulted in attenuated virulence. Furthermore, the acquisition of new alternative PBMs after a number of cell passages confirmed the key importance of the binding with PDZ proteins for the virus activity. Interaction occurring between SARS-CoV E protein and PDZ domains of PALS1 and syntenin  as well as with other PDZ-containing proteins such as TJP1-2, PTPN13, HTRA1, MLLT4, PARD3, LNX2, recognizing the PBM of SARS-CoV E protein, and NHERF1, MAST2, RADIL, SNX27 as specific interactors of SARS-CoV-2 E protein  has been reported.
The interaction of E protein with PALS1 is of particular importance. PALS1 is a member of MAGUK superfamily and it is the human homologue of D. melanogaster Stardust protein. It is composed of two N-terminal L27 domains, followed by a PDZ domain, a SH3 domain and a guanylate kinase domain (GUK). PALS1 possesses a central role in determining the Crumbs polarity complex, which, in its entirety, is composed of a transmembrane protein (Crumbs) and two cytoplasmic scaffolding proteins, PATJ and PALS1. The association of PALS1 with Crumbs is mediated by PDZ, SH3 and GUK domain supramodular structure , determining the apical portion of epithelial cells, together with the interaction with PATJ and MUPP1 [169, 170]. The interaction between PALS1 PDZ domain and the E protein of SARS-CoV (and SARS-CoV-2) is suggested to be at the basis of lung epithelial damage [163, 165], retaining the protein in Golgi vesicles after synthesis, and preventing the correct formation of tight junctions. As a result, a diffuse damage of lung epithelial tissue occurs, representing one of the most dramatic and fatal outcomes of coronavirus infections. Given these premises, reinforced by the global health emergency due to SARS-CoV-2 spread and the severity of COVID-19 pandemic, the PDZ domain of PALS1 represents a strategic site to be pharmacologically targeted.
The three dimensional structure of the PALS1:E protein complex has been recently resolved  and outlined a synergistic mechanism of ligand recognition exerted by PDZ and SH3 domains. Recent studies showed a higher affinity of E protein from SARS-CoV-2 compared to SARS-CoV for the isolated PDZ domain of PALS1 [172, 173]. Molecular Dynamics simulations highlighted the SARS-CoV-2 Arginine 69 as key residue responsible of the improved affinity to PALS1 compared to the SARS-CoV homologue, in particular by enhancing polar interactions with negatively charged pockets of PALS1 PDZ domain, resulting in significantly reduced mobility of the viral protein. These data supported the hypothesis that the typical virulence of SARS-CoV-2 may rely on the improved binding of E protein with PALS1 and represent a first step in understanding the mechanistic details of this important interaction, which should be further investigated to develop potential SARS-CoV-2 antiviral strategies.
Oncogenic viral PDZ domain interacting proteins
As detailed in paragraph 2.1, a large number of PDZ-containing proteins possess key roles in the maintenance of the correct physiology of the cell at different levels, ranging from transcription factors to scaffolding proteins and to polarity determination of specialized cells. Consequently, viruses expressing proteins able to target PDZ domains are often correlated with the onset of cancer pathologies.
There are several examples of viruses exerting their oncogenic activity by targeting PDZ containing proteins, as for example Hepatitis C virus , Hepatitis B virus [159, 160] and Human T Cell Leukemia Virus 1 [155, 161]. However, one of the most studied and characterized PDZ interacting viral proteins is the E6 protein from HPV (Human Papillomavirus) (Fig. 2). Despite over 200 different strains of Papillomaviruses being identified, only a small subset (around 30) of them are reported as carcinogenic, denoted as high-risk HPVs. Interestingly, only high-risk HPVs contain a PDZ-binding motif at the C-terminus of their E6 protein, highlighting the importance of PDZ mediated interaction in the tumorigenic progress of these viruses infection.
The principal event in tumorigenic activity of E6 is its ability to inactivate tumor suppressor p53 protein [174, 175]. Furthermore, many PDZ proteins with key roles in cell proliferation, cell growth, cell polarity and protein degradation are reported as interactors of E6 high-risk HPVs . For such reasons, a number of studies have focused on understanding the binding process of E6 proteins with PDZ domains and the molecular details of this interaction . In general, carcinogenic activity of high-risk HPVs is achieved through the interaction between E6 and PDZ domain of SAP-97 and Scribble proteins. Recently, the ability of high-risk HPV-16 and HPV-18 E6 proteins to target the PDZ domain of NHERF2 has been reported . NHERF2 is a tumor suppressor protein which, among other functions in the cell, regulates endothelial proliferation. Since in transformed cells apoptosis is prevented only as long as the expression of E6 and E7 are sustained in the host cell, PDZ domains interacting with E6 proteins represent promising drug targets to contrast the tumorigenic activity of high-risk HPVs.
Protein-Engineering optimized PDZ domain as pharmacological strategy
With the final goal to bind and sequester E6 protein from high-risk HPV18 and prevent it to interact with host cell targets, a recombinant optimized PDZ domain was conceived and produced (named "PDZbody") by designing a chimeric domain composed of a strategically mutated PDZ domain fused with an extra alpha helix from E6AP (E6-associated protein), a different interactor of E6 protein in the host cell . This engineered PDZbody allowed to target two different sites of the E6 proteins, with an increased affinity compared to its natural interactors . This strategy reported promising results both in in vitro and in cellula experiments, confirming the ability of PDZbody to trap E6 protein from interacting with host cell proteins. By following an analogous approach, a protein chimera composed of the PDZ2 domain of the tight-junction protein MAGI1 and the LxxLL motif of E6AP was designed to disrupt E6 interactions in the host cells . Although these strategies represent an important starting point in the attempt to hijack the oncogenic activity of high-risk HPVs, the diversity of sequences of E6 proteins among the high-risk HPVs family and the several PDZ domains involved in the pathogenic pathways makes an arduous effort to develop focused pharmacological therapies and further experimental efforts are demanded in order to step forward to this goal.
The crucial role played by PDZ domain in the spreading of cellular signals and their aberrant activations in many human diseases makes the PDZ domains very attractive targets for drug discovery (a summarizing list of PDZ-containing proteins involved in human pathologies is reported in Table 1). Thus, the discovery of small molecules able to impar the protein–protein interactions in which PDZs are involved, proved to be very profitable, rather than targeting entire signaling cascades, as typically achieved by receptor antagonists. Efforts in the identification of modulators of the PDZ signals has widely increased in the last years. Since 1996, when it was reported the first peptide able to bind a PDZ domain  more than 600 papers about PDZ inhibitors were published (source SciFinder). Among them, many remarkable results were reported such as the PDZ inhibitors of PSD-95 , Synthenin  and Dvl [69, 70]. More than 600 crystal structures of human PDZ domains available at the protein data bank (ww.rcsb.org) have brought significant insight into the rational design of PDZ modulators. This structural information encouraged the use of molecular modelling studies. Virtual screening is highly used to identify PDZ inhibitors; indeed, it is possible to use the cognate substrate of the targeted PDZ to design a pharmacophore model by which selecting the studied compounds [182,183,184].
Despite the promising results, at the state of the art, no small molecules are in clinical or preclinical phase. It may be due to: (i) the wider surface of the binding pocket, making difficult to reach with high affinity the binding site by a small molecule [71, 185]; (ii) the promiscuity of the PDZ domains making selectivity a big concern ; and (iii) the post translational modifications, such as phosphorylation, which have shown to be potent modifiers of binding affinities to PDZ domains and can either decrease or enhance affinity . On the other hand, a large number of peptides and peptidomimetics have been evaluated as PDZ modulators. The most successful story is about NA-1. It is a peptide inhibitor of the PDS-95 PDZ2 with Ki of 4.4 μM. . NA-1 (NH2-YGRKKRRQRRRKLSSIESDV-COOH) was designed as a fusion peptide bearing a PDZ binding sequence obtained from the cognate substrate GluN2B NMDAR and a Tat peptide to increase the cell permeability. In phase II clinical studies, NA-1 reduced the number of heart attacks in patients at risk of embolic stroke . Worthy of note, the studies about PSD-95 led to a new paradigm in the design of PDZ inhibitors. The very similar structures of PDZ1 and PDZ2 suggested the development of a tandem binder. Starting from the cognate substrate GluN2B, a pentapeptide (IETAV) was identified which dimerized through a PEG linker leading to derivative AVLX-125, with 145-fold improved binding affinity compared with the monomer. and a Ki of 10 nM . Later, the same authors reported a trimeric peptide by adding another branch to AVLX-125. The added peptide (YKQTSV) was different from the previous one, because the PSD-95 PDZ3 had a lower homology with the other PDZ domains. The tripeptide showed a higher affinity compared to the dimer with a Ki close to 3 nM  (Fig. 5).
The crucial role played by DVL in the cancer development, progression, metastasis and chemotherapy resistance  prompted great effort in the development of small molecules able to impair this aberrant PDZ dependent activity. As a result, a large number of DVL small molecule inhibitors were synthesized. The first one, NSC6680036 reported in 2005 , was discovered by a structure based virtual screening and the mechanism of action was confirmed by NMR studies . NSC6680036 derivatives were not further developed because of their peptidomimetic rather than small molecule strcuture. Later, the same authors reported derivative J01-017a, identified by virtual screening and 3D QSAR methods, with improved binding affinity (Kd 1.5 μM)  and FJ9 (DVL3 Kd 26 μM) . The latter derivative had an indole/indene-carboxylic acid scaffold which was conserved, with minor modification, in many DVL PDZ inhibitors, such as the non steroidal antinflammatory drug sulindac (Kd 11 μM) and KY02061 (IC50 24 μM) . In general, nonsteroidal anti-inflammatory compounds showed the ability to suppress the Wnt pathway in breast, colon and lung cancers . KY02061 identified by virtual screening approach, impaired the Dvl–CXXC5 interaction by binding the PDZ domain, and increased of the β-catenin nuclear concentration favoring the bone anabolic activity . Mahindroo et al.  reported an indole based DVL PDZ inhibitor designed by mimicking the peptide sequence of the substrate. The most active compound, 6e, an indole-2-carboxamide-5-carboxylic acid derivative, showed IC50 values of 23 and 49 μM for DVL3 and DVL1, respectively (Fig. 6).
Benzofused heterocycles were reported as privileged scaffolds for the inhibition of PDZ of the DVL: indole and indazole with Kd in the one-digit micromolar range for DVL1 by Kandem (https://doi.org/10.5194/mr-2-355-2021), and benzothiophenone derivatives (i.e. BMD4602 with Kd of 11 μM) by Choi . The indole ring seems to fit well in the binding pocket of the PDZ. Generally speaking, the benzofused scaffold (benzene plus a 5-menber heterocyclic ring) allows to generate a variety of diverse compound libraries with potential high binding affinity and selectivity towards the PDZ family. Indole derivatives were also reported as inhibitors of some other PDZ domains . Representative examples are reported in a series of papers by Fujii et al. By docking analysis the authors identified an irreversible inhibitor of membrane-associated guanylate kinase 3 (MAGI3) PDZ2. The biological activity of this inhibitor assayed in HTC116 cells and the binding was confirmed by mass spectrometry experiments . Introduction of appropriate substituents at position(s) 1, 2 and 3 of the indole ring shifted the targeted PDZ from MAGI3 to DVLs (6e)  (for examples, see Figs. 6 and 7). A derivative with different substituent at the indole showed high binding affinity for both PDZ domain of NHERF1 in the micromolar range . This example well illustrates the possibility to modulate the desired biological activity by changing substituents of the core skeleton. At the same time, it rises a not negligible problem of selectivity among the PDZ domains.
The growing interest for PDZ modulators over the past years is due to their vast therapeutic potential (Table 2). However, despite several hit-compounds have been discovered, none of them entered the clinic stages, suggesting that the optimization of initial hit-compounds is not trivial. Overall, the drug discovery community have the opportunity to step up to the challenge posed by the development of PDZ inhibitors as new treatments for still unsolved diseases.
PDZ domains are the most diffused structural and functional protein modules mediating protein–protein interactions, and they serve as fundamental elements in the construction of the cellular molecular machinery. Because of their importance in several molecular and physiological pathways, misregulation of PDZ-mediated interactions causes the onset of many pathologies. Thus, PDZ domains represent interesting drug targets and the inhibition of their interactions is an important pharmacological strategy to treat those pathologies.
A continuously increasing effort from the scientific community allowed the development of brilliant experimental strategies aimed to target PDZ domains. However, difficulties arose during the years to achieve this goal, ranging from the generally low binding selectivity of PDZ domains, which prevented the targeting of a specific PDZ domain, to the scarce efficiency of small molecules in inhibiting PDZ binding. As already described in paragraph 1.1 PDZ domains can be generally classified in three classes based on their binding specificity, depending on the sequence of the recognized protein. However, a proteomic analysis conducted on mouse PDZ domains demonstrated this classification to be superficial, specificity of PDZ domains being particularly broad , multiple residues, probably arranged in the binding pocket, driving selectivity. In particular, residues 0 and -2 were shown to possess key role in determining affinity, while residues -4, -3, -2 and -1 seem to orchestrate the selectivity of the recognition  with overlapping consensus sequences among the domain family. As an illustrative example of the complexity of successful inhibition of PDZ domains, in order to improve affinity and selectivity in targeting PDZ domain of CAL and avoid cross-reactivity, the design of a selective inhibitor of CFTR-CAL binding (showed in Fig. 3), required not just a “C-terminal core” (-4, -3, -2, -1, 0) to be taken into account, but also residues upstream (-9,-8,-7,-6,-5) were found to be fundamental .
Under this light, it appears clear that achieving a controlled selectivity in targeting of PDZ domain appears to be a difficult but crucial task, in order to decrease cross-reactivity and improve efficacy in therapies based on the inhibition of PDZ-containing proteins. Nevertheless, given the importance of PDZ domains in several human pathologies, further theoretical and experimental investigations are required in order to develop feasible and efficient drugs able to regulate and inhibit PDZ mediated interactions.
Availability of data and materials
Copley RR, Doerks T, Letunic I, Bork P. Protein domain analysis in the era of complete genomes. FEBS Lett. 2002;513:129–34.
Jadwin JA, Ogiue-Ikeda M, Machida K. The application of modular protein domains in proteomics. FEBS Lett. 2012;586:2586–96.
Songyang Z, Shoelson SE, Chaudhuri M, Gish G, Pawson T, Haser WG, et al. SH2 domains recognize specific phosphopeptide sequences. Cell. 1993;72:767–78.
Kavanaugh WM, Williams LT. An alternative to SH2 domains for binding tyrosine-phosphorylated proteins. Science. 1994;266:1862–5.
Blaikie P, Immanuel D, Wu J, Li N, Yajnik V, Margolis B. A region in Shc distinct from the SH2 domain can bind tyrosine-phosphorylated growth factor receptors. J Biol Chem. 1994;269:32031–4.
Yaffe MB, Elia AE. Phosphoserine/threonine-binding domains. Curr Opin Cell Biol. 2001;13:131–8.
Zeng L, Zhou MM. Bromodomain: an acetyl-lysine binding domain. FEBS Lett. 2002;513:124–8.
Yap KL, Zhou M-M. Structure and mechanisms of lysine methylation recognition by the chromodomain in gene transcription. Biochemistry. 2011;50:1966–80.
Marmorstein R. Protein modules that manipulate histone tails for chromatin regulation. Nat Rev Mol Cell Biol. 2001;2:422–32.
Ren R, Mayer BJ, Cicchetti P, Baltimore D. Identification of a ten-amino acid proline-rich SH3 binding site. Science. 1993;259:1157–61.
Macias MJ, Wiesner S, Sudol M. WW and SH3 domains, two different scaffolds to recognize proline-rich ligands. FEBS Lett. 2002;513:30–7.
Sudol M. From Src Homology domains to other signaling modules: proposal of the “protein recognition code.” Oncogene. 1998;17:1469–74.
Park HH, Lo Y-C, Lin S-C, Wang L, Yang JK, Wu H. The death domain superfamily in intracellular signaling of apoptosis and inflammation. Annu Rev Immunol. 2007;25:561–86.
Barnhart BC, Lee JC, Alappat EC, Peter ME. The death effector domain protein family. Oncogene. 2003;22:8634–44.
Hofmann K, Bucher P, Tschopp J. The CARD domain: a new apoptotic signalling motif. Trends Biochem Sci. 1997;22:155–6.
Reed JC, Zha H, Aime-Sempe C, Takayama S, Wang HG. Structure-function analysis of Bcl-2 family proteins. Regulators of programmed cell death. Adv Exp Med Biol. 1996;406:99–112.
Kofler MM, Freund C. The GYF domain. FEBS J. 2006;273:245–56.
Weimbs T, Low SH, Chapin SJ, Mostov KE, Bucher P, Hofmann K. A conserved domain is present in different families of vesicular fusion proteins: a new superfamily. Proc Natl Acad Sci U S A. 1997;94:3046–51.
Lohi O, Poussu A, Mao Y, Quiocho F, Lehto VP. VHS domain – a longshoreman of vesicle lines. FEBS Lett. 2002;513:19–23.
Kim CA, Bowie JU. SAM domains: uniform structure, diversity of function. Trends Biochem Sci. 2003;28:625–8.
Amacher JF, Brooks L, Hampton TH, Madden DR. Specificity in PDZ-peptide interaction networks: computational analysis and review. J Struct Biol X. 2020;4:100022.
Kennedy MB. Origin of PDZ (DHR, GLGF) domains. Trends Biochem Sci. 1995;20:350.
Kennedy MB. The postsynaptic density at glutamatergic synapses. Trends Neurosci. 1997;20:264–8.
Cho KO, Hunt CA, Kennedy MB. The rat brain postsynaptic density fraction contains a homolog of the Drosophila discs-large tumor suppressor protein. Neuron. 1992;9:929–42.
Songyang Z, Fanning AS, Fu C, Xu J, Marfatia SM, Chishti AH, et al. Recognition of unique carboxyl-terminal motifs by distinct PDZ domains. Science. 1997;275:73–7.
Liu X, Fuentes EJ. Emerging themes in PDZ domain signaling: structure, function, and inhibition. Int Rev Cell Mol Biol. 2019;343:129–218.
Cohen NA, Brenman JE, Snyder SH, Bredt DS. Binding of the inward rectifier K+ channel Kir 2.3 to PSD-95 is regulated by protein kinase A phosphorylation. Neuron. 1996;17:759–67.
Zimmermann P, Meerschaert K, Reekmans G, Leenaerts I, Small JV, Vandekerckhove J, et al. PIP(2)-PDZ domain binding controls the association of syntenin with the plasma membrane. Mol Cell. 2002;9:1215–25.
Penkert RR, DiVittorio HM, Prehoda KE. Internal recognition through PDZ domain plasticity in the Par-6-Pals1 complex. Nat Struct Mol Biol. 2004;11:1122–7.
Hillier BJ, Christopherson KS, Prehoda KE, Bredt DS, Lim WA. Unexpected modes of PDZ domain scaffolding revealed by structure of nNOS-syntrophin complex. Science. 1999;284:812–5.
Craven SE, Bredt DS. PDZ proteins organize synaptic signaling pathways. Cell. 1998;93:495–8.
Labouesse M. The yeast mitochondrial leucyl-tRNA synthetase is a splicing factor for the excision of several group I introns. Mol Gen Genet MGG. 1990;224:209–21.
Halaoui R, McCaffrey L. Rewiring cell polarity signaling in cancer. Oncogene. 2015;34:939–50.
Subbaiah VK, Kranjec C, Thomas M, Banks L. PDZ domains: the building blocks regulating tumorigenesis. Biochem J. 2011;439:195–205.
Hartsock A, Nelson WJ. Adherens and tight junctions: structure, function and connections to the actin cytoskeleton. Biochim Biophys Acta. 2008;1778:660–9.
Bilder D. Epithelial polarity and proliferation control: links from the Drosophila neoplastic tumor suppressors. Genes Dev. 2004;18:1909–25.
Campbell HK, Maiers JL, DeMali KA. Interplay between tight junctions & adherens junctions. Exp Cell Res. 2017;358:39–44.
Martin TA, Jiang WG. Loss of tight junction barrier function and its role in cancer metastasis. Biochim Biophys Acta. 2009;1788:872–91.
Kapil S, Sharma BK, Patil M, Elattar S, Yuan J, Hou SX, et al. The cell polarity protein Scrib functions as a tumor suppressor in liver cancer. Oncotarget. 2017;8:26515–31.
Feng X, Jia S, Martin TA, Jiang WG. Regulation and involvement in cancer and pathological conditions of MAGI1, a tight junction protein. Anticancer Res. 2014;34:3251–6.
Zaric J, Joseph J-M, Tercier S, Sengstag T, Ponsonnet L, Delorenzi M, et al. Identification of MAGI1 as a tumor-suppressor protein induced by cyclooxygenase-2 inhibitors in colorectal cancer cells. Oncogene. 2012;31:48–59.
Kwan J, Sczaniecka A, Heidary Arash E, Nguyen L, Chen C-C, Ratkovic S, et al. DLG5 connects cell polarity and Hippo signaling protein networks by linking PAR-1 with MST1/2. Genes Dev. 2016;30:2696–709.
Liu J, Li J, Li P, Wang Y, Liang Z, Jiang Y, et al. Loss of DLG5 promotes breast cancer malignancy by inhibiting the Hippo signaling pathway. Sci Rep. 2017;7:42125.
Santoni M-J, Kashyap R, Camoin L, Borg J-P. The Scribble family in cancer: twentieth anniversary. Oncogene. 2020;39:7019–33.
Zhang X, Wang L, Zhang H, Tu F, Qiang Y, Nie C. Decreased expression of ZO-1 is associated with tumor metastases in liver cancer. Oncol Lett. 2019;17:1859–64.
González-Mariscal L, Gallego-Gutiérrez H, González-González L, Hernández-Guzmán C. ZO-2 is a master regulator of gene expression, cell proliferation, cytoarchitecture, and cell size. Int J Mol Sci. 2019;20:4128.
Facciuto F, Cavatorta AL, Valdano MB, Marziali F, Gardiol D. Differential expression of PDZ domain-containing proteins in human diseases - challenging topics and novel issues. FEBS J. 2012;279:3538–48.
Roberts S, Delury C, Marsh E. The PDZ protein discs-large (DLG): the “Jekyll and Hyde” of the epithelial polarity proteins. FEBS J. 2012;279:3549–58.
Valiente M, Andrés-Pons A, Gomar B, Torres J, Gil A, Tapparel C, et al. Binding of PTEN to specific PDZ domains contributes to PTEN protein stability and phosphorylation by microtubule-associated serine/threonine kinases. J Biol Chem. 2005;280:28936–43.
Takahashi Y, Morales FC, Kreimann EL, Georgescu M-M. PTEN tumor suppressor associates with NHERF proteins to attenuate PDGF receptor signaling. EMBO J. 2006;25:910–20.
Kotelevets L, Scott MGH, Chastre E. Targeting PTEN in colorectal cancers. Adv Exp Med Biol. 2018;1110:55–73.
Kuang S-Q, Tong W-G, Yang H, Lin W, Lee MK, Fang ZH, et al. Genome-wide identification of aberrantly methylated promoter associated CpG islands in acute lymphocytic leukemia. Leukemia. 2008;22:1529–38.
Kegelman TP, Das SK, Hu B, Bacolod MD, Fuller CE, Menezes ME, et al. MDA-9/syntenin is a key regulator of glioma pathogenesis. Neuro-Oncol. 2014;16:50–61.
Kegelman TP, Das SK, Emdad L, Hu B, Menezes ME, Bhoopathi P, et al. Targeting tumor invasion: the roles of MDA-9/Syntenin. Expert Opin Ther Targets. 2015;19:97–112.
Boukerche H, Aissaoui H, Prévost C, Hirbec H, Das SK, Su Z-Z, et al. Src kinase activation is mandatory for MDA-9/syntenin-mediated activation of nuclear factor-kappaB. Oncogene. 2010;29:3054–66.
Storz P, Toker A. Protein kinase D mediates a stress-induced NF-kappaB activation and survival pathway. EMBO J. 2003;22:109–20.
Menezes ME, Shen X-N, Das SK, Emdad L, Sarkar D, Fisher PB. MDA-9/Syntenin (SDCBP) modulates small GTPases RhoA and Cdc42 via transforming growth factor β1 to enhance epithelial-mesenchymal transition in breast cancer. Oncotarget. 2016;7:80175–89.
Liu J, Qu J, Zhou W, Huang Y, Jia L, Huang X, et al. Syntenin-targeted peptide blocker inhibits progression of cancer cells. Eur J Med Chem. 2018;154:354–66.
Haugaard-Kedström LM, Clemmensen LS, Sereikaite V, Jin Z, Fernandes EFA, Wind B, et al. A high-affinity peptide ligand targeting syntenin inhibits glioblastoma. J Med Chem. 2021;64:1423–34.
Romero G, von Zastrow M, Friedman PA. Role of PDZ proteins in regulating trafficking, signaling, and function of GPCRs: means, motif, and opportunity. Adv Pharmacol San Diego Calif. 2011;62:279–314.
Caretta A, Mucignat-Caretta C. Protein kinase a in cancer. Cancers. 2011;3:913–26.
Owusu Obeng E, Rusciano I, Marvi MV, Fazio A, Ratti S, Follo MY, et al. Phosphoinositide-dependent signaling in cancer: a focus on phospholipase C isozymes. Int J Mol Sci. 2020;21:2581.
Wong H-C, Bourdelas A, Krauss A, Lee H-J, Shao Y, Wu D, et al. Direct binding of the PDZ domain of Dishevelled to a conserved internal sequence in the C-terminal region of Frizzled. Mol Cell. 2003;12:1251–60.
Clevers H, Nusse R. Wnt/β-catenin signaling and disease. Cell. 2012;149:1192–205.
Veeman MT, Axelrod JD, Moon RT. A second canon Functions and mechanisms of beta-catenin-independent Wnt signaling. Dev Cell. 2003;5:367–77.
Weeraratna AT, Jiang Y, Hostetter G, Rosenblatt K, Duray P, Bittner M, et al. Wnt5a signaling directly affects cell motility and invasion of metastatic melanoma. Cancer Cell. 2002;1:279–88.
Yuzugullu H, Benhaj K, Ozturk N, Senturk S, Celik E, Toylu A, et al. Canonical Wnt signaling is antagonized by noncanonical Wnt5a in hepatocellular carcinoma cells. Mol Cancer. 2009;8:90.
Fujii N, You L, Xu Z, Uematsu K, Shan J, He B, et al. An antagonist of dishevelled protein-protein interaction suppresses beta-catenin-dependent tumor cell growth. Cancer Res. 2007;67:573–9.
Mahindroo N, Punchihewa C, Bail AM, Fujii N. Indole-2-amide based biochemical antagonist of Dishevelled PDZ domain interaction down-regulates Dishevelled-driven Tcf transcriptional activity. Bioorg Med Chem Lett. 2008;18:946–9.
Zhang Y, Appleton BA, Wiesmann C, Lau T, Costa M, Hannoush RN, et al. Inhibition of Wnt signaling by Dishevelled PDZ peptides. Nat Chem Biol. 2009;5:217–9.
Christensen NR, Čalyševa J, Fernandes EFA, Lüchow S, Clemmensen LS, Haugaard-Kedström LM, et al. PDZ domains as drug targets. Adv Ther. 2019;2:1800143.
Chittenden TW, Pak J, Rubio R, Cheng H, Holton K, Prendergast N, et al. Therapeutic implications of GIPC1 silencing in cancer. PLoS ONE. 2010;5:e15581.
Centonze M, Saponaro C, Mangia A. NHERF1 between promises and hopes: overview on cancer and prospective openings. Transl Oncol. 2018;11:374–90.
Srijakotre N, Liu H-J, Nobis M, Man J, Yip HYK, Papa A, et al. PtdIns(3,4,5)P3-dependent Rac exchanger 1 (P-Rex1) promotes mammary tumor initiation and metastasis. Proc Natl Acad Sci USA. 2020;117:28056–67.
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245:1066–73.
Sheppard DN, Welsh MJ. Structure and function of the CFTR chloride channel. Physiol Rev. 1999;79:S23-45.
Saint-Criq V, Gray MA. Role of CFTR in epithelial physiology. Cell Mol Life Sci CMLS. 2017;74:93–115.
Guggino WB. Cystic fibrosis and the salt controversy. Cell. 1999;96:607–10.
Riordan JR. CFTR function and prospects for therapy. Annu Rev Biochem. 2008;77:701–26.
Boucher RC. Airway surface dehydration in cystic fibrosis: pathogenesis and therapy. Annu Rev Med. 2007;58:157–70.
Cheng J, Moyer BD, Milewski M, Loffing J, Ikeda M, Mickle JE, et al. A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression. J Biol Chem. 2002;277:3520–9.
Guggino WB. The cystic fibrosis transmembrane regulator forms macromolecular complexes with PDZ domain scaffold proteins. Proc Am Thorac Soc. 2004;1:28–32.
Cheng J, Wang H, Guggino WB. Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CAL. J Biol Chem. 2004;279:1892–8.
Cheng J, Cebotaru V, Cebotaru L, Guggino WB. Syntaxin 6 and CAL mediate the degradation of the cystic fibrosis transmembrane conductance regulator. Mol Biol Cell. 2010;21:1178–87.
Raghuram V, Mak DO, Foskett JK. Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction. Proc Natl Acad Sci USA. 2001;98:1300–5.
Guggino WB, Stanton BA. New insights into cystic fibrosis: molecular switches that regulate CFTR. Nat Rev Mol Cell Biol. 2006;7:426–36.
Lukacs GL, Verkman AS. CFTR: folding, misfolding and correcting the ΔF508 conformational defect. Trends Mol Med. 2012;18:81–91.
Pedemonte N, Lukacs GL, Du K, Caci E, Zegarra-Moran O, Galietta LJV, et al. Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening. J Clin Invest. 2005;115:2564–71.
Van Goor F, Straley KS, Cao D, González J, Hadida S, Hazlewood A, et al. Rescue of DeltaF508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules. Am J Physiol Lung Cell Mol Physiol. 2006;290:L1117-1130.
Wolde M, Fellows A, Cheng J, Kivenson A, Coutermarsh B, Talebian L, et al. Targeting CAL as a negative regulator of DeltaF508-CFTR cell-surface expression: an RNA interference and structure-based mutagenetic approach. J Biol Chem. 2007;282:8099–109.
Vouilleme L, Cushing PR, Volkmer R, Madden DR, Boisguerin P. Engineering peptide inhibitors to overcome PDZ binding promiscuity. Angew Chem Int Ed Engl. 2010;49:9912–6.
Cushing PR, Vouilleme L, Pellegrini M, Boisguerin P, Madden DR. A stabilizing influence: CAL PDZ inhibition extends the half-life of ΔF508-CFTR. Angew Chem Int Ed Engl. 2010;49:9907–11.
Dougherty PG, Wellmerling JH, Koley A, Lukowski JK, Hummon AB, Cormet-Boyaka E, et al. Cyclic peptidyl inhibitors against CAL/CFTR interaction for treatment of cystic fibrosis. J Med Chem. 2020;63:15773–84.
Sheng M, Kim MJ. Postsynaptic signaling and plasticity mechanisms. Science. 2002;298:776–80.
Santos R, Ursu O, Gaulton A, Bento AP, Donadi RS, Bologa CG, et al. A comprehensive map of molecular drug targets. Nat Rev Drug Discov. 2017;16:19–34.
Rosenbaum MI, Clemmensen LS, Bredt DS, Bettler B, Strømgaard K. Targeting receptor complexes: a new dimension in drug discovery. Nat Rev Drug Discov. 2020;19:884–901.
Kim E, Sheng M. PDZ domain proteins of synapses. Nat Rev Neurosci. 2004;5:771–81.
Garner CC, Nash J, Huganir RL. PDZ domains in synapse assembly and signalling. Trends Cell Biol. 2000;10:274–80.
McGee AW, Bredt DS. Assembly and plasticity of the glutamatergic postsynaptic specialization. Curr Opin Neurobiol. 2003;13:111–8.
Brenman JE, Chao DS, Gee SH, McGee AW, Craven SE, Santillano DR, et al. Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains. Cell. 1996;84:757–67.
Han K, Kim E. Synaptic adhesion molecules and PSD-95. Prog Neurobiol. 2008;84:263–83.
El-Husseini AE, Schnell E, Chetkovich DM, Nicoll RA, Bredt DS. PSD-95 involvement in maturation of excitatory synapses. Science. 2000;290:1364–8.
Dev KK. Making protein interactions druggable: targeting PDZ domains. Nat Rev Drug Discov. 2004;3:1047–56.
Toro R, Konyukh M, Delorme R, Leblond C, Chaste P, Fauchereau F, et al. Key role for gene dosage and synaptic homeostasis in autism spectrum disorders. Trends Genet TIG. 2010;26:363–72.
Coley AA, Gao W-J. PSD95: a synaptic protein implicated in schizophrenia or autism? Prog Neuropsychopharmacol Biol Psychiatry. 2018;82:187–94.
Feng W, Zhang M. Organization and dynamics of PDZ-domain-related supramodules in the postsynaptic density. Nat Rev Neurosci. 2009;10:87–99.
Zhang J, Lewis SM, Kuhlman B, Lee AL. Supertertiary structure of the MAGUK core from PSD-95. Struct Lond Engl. 1993;2013(21):402–13.
McGee AW, Dakoji SR, Olsen O, Bredt DS, Lim WA, Prehoda KE. Structure of the SH3-guanylate kinase module from PSD-95 suggests a mechanism for regulated assembly of MAGUK scaffolding proteins. Mol Cell. 2001;8:1291–301.
Funke L, Dakoji S, Bredt DS. Membrane-associated guanylate kinases regulate adhesion and plasticity at cell junctions. Annu Rev Biochem. 2005;74:219–45.
Tsai N-P, Wilkerson JR, Guo W, Maksimova MA, DeMartino GN, Cowan CW, et al. Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95. Cell. 2012;151:1581–94.
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 2014;515:209–15.
Gilman SR, Iossifov I, Levy D, Ronemus M, Wigler M, Vitkup D. Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron. 2011;70:898–907.
Monteiro P, Feng G. SHANK proteins: roles at the synapse and in autism spectrum disorder. Nat Rev Neurosci. 2017;18:147–57.
Peça J, Feliciano C, Ting JT, Wang W, Wells MF, Venkatraman TN, et al. Shank3 mutant mice display autistic-like behaviours and striatal dysfunction. Nature. 2011;472:437–42.
Schmeisser MJ, Ey E, Wegener S, Bockmann J, Stempel AV, Kuebler A, et al. Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2. Nature. 2012;486:256–60.
Boccuto L, Lauri M, Sarasua SM, Skinner CD, Buccella D, Dwivedi A, et al. Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. Eur J Hum Genet EJHG. 2013;21:310–6.
Yang M, Bozdagi O, Scattoni ML, Wöhr M, Roullet FI, Katz AM, et al. Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice. J Neurosci Off J Soc Neurosci. 2012;32:6525–41.
Hung AY, Futai K, Sala C, Valtschanoff JG, Ryu J, Woodworth MA, et al. Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1. J Neurosci Off J Soc Neurosci. 2008;28:1697–708.
Dobson CM, Knowles TP, Vendruscolo M. The amyloid phenomenon and its significance in biology and medicine. Cold Spring Harb Perspect Biol. 2019. https://doi.org/10.1101/cshperspect.a033878.
Chiti F, Dobson CM. Protein misfolding, amyloid formation, and human disease: a summary of progress over the last decade. Annu Rev Biochem. 2017;86:27–68.
Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer’s disease: progress and problems on the road to therapeutics. Science. 2002;297:353–6.
Knowles TP, Vendruscolo M, Dobson CM. The amyloid state and its association with protein misfolding diseases. Nat Rev Mol Cell Biol. 2014;15:384–96.
Sastre M, Turner RS, Levy E. X11 interaction with beta-amyloid precursor protein modulates its cellular stabilization and reduces amyloid beta-protein secretion. J Biol Chem. 1998;273:22351–7.
Tomita S, Ozaki T, Taru H, Oguchi S, Takeda S, Yagi Y, et al. Interaction of a neuron-specific protein containing PDZ domains with Alzheimer’s amyloid precursor protein. J Biol Chem. 1999;274:2243–54.
Miller CCJ, McLoughlin DM, Lau K-F, Tennant ME, Rogelj B. The X11 proteins, Abeta production and Alzheimer’s disease. Trends Neurosci. 2006;29:280–5.
Long J-F, Feng W, Wang R, Chan L-N, Ip FCF, Xia J, et al. Autoinhibition of X11/Mint scaffold proteins revealed by the closed conformation of the PDZ tandem. Nat Struct Mol Biol. 2005;12:722–8.
Borg JP, Ooi J, Levy E, Margolis B. The phosphotyrosine interaction domains of X11 and FE65 bind to distinct sites on the YENPTY motif of amyloid precursor protein. Mol Cell Biol. 1996;16:6229–41.
King GD, Perez RG, Steinhilb ML, Gaut JR, Turner RS. X11alpha modulates secretory and endocytic trafficking and metabolism of amyloid precursor protein: mutational analysis of the YENPTY sequence. Neuroscience. 2003;120:143–54.
Lau KF, McLoughlin DM, Standen C, Miller CC. X11 alpha and x11 beta interact with presenilin-1 via their PDZ domains. Mol Cell Neurosci. 2000;16:557–65.
Biederer T, Cao X, Südhof TC, Liu X. Regulation of APP-dependent transcription complexes by Mint/X11s: differential functions of Mint isoforms. J Neurosci Off J Soc Neurosci. 2002;22:7340–51.
Sullivan SE, Dillon GM, Sullivan JM, Ho A. Mint proteins are required for synaptic activity-dependent amyloid precursor protein (APP) trafficking and amyloid β generation. J Biol Chem. 2014;289:15374–83.
Poewe W, Seppi K, Tanner CM, Halliday GM, Brundin P, Volkmann J, et al. Parkinson disease. Nat Rev Dis Primer. 2017;3:17013.
Balestrino R, Schapira AHV. Parkinson disease. Eur J Neurol. 2020;27:27–42.
Fusco G, Chen SW, Williamson PTF, Cascella R, Perni M, Jarvis JA, et al. Structural basis of membrane disruption and cellular toxicity by α-synuclein oligomers. Science. 2017;358:1440–3.
Alnemri ES. HtrA2 and Parkinson’s disease: think PINK? Nat Cell Biol. 2007;9:1227–9.
Toyama Y, Harkness RW, Lee TYT, Maynes JT, Kay LE. Oligomeric assembly regulating mitochondrial HtrA2 function as examined by methyl-TROSY NMR. Proc Natl Acad Sci USA. 2021;118:e2025022118.
Schlieker C, Mogk A, Bukau B. A PDZ switch for a cellular stress response. Cell. 2004;117:417–9.
Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, et al. Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson’s disease. Hum Mol Genet. 2005;14:2099–111.
Unal Gulsuner H, Gulsuner S, Mercan FN, Onat OE, Walsh T, Shahin H, et al. Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proc Natl Acad Sci USA. 2014;111:18285–90.
Jones JM, Datta P, Srinivasula SM, Ji W, Gupta S, Zhang Z, et al. Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice. Nature. 2003;425:721–7.
Martins LM, Morrison A, Klupsch K, Fedele V, Moisoi N, Teismann P, et al. Neuroprotective role of the Reaper-related serine protease HtrA2/Omi revealed by targeted deletion in mice. Mol Cell Biol. 2004;24:9848–62.
Géléoc GGS, El-Amraoui A. Disease mechanisms and gene therapy for Usher syndrome. Hear Res. 2020;394:107932.
Yang J, Liu X, Zhao Y, Adamian M, Pawlyk B, Sun X, et al. Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss. PLoS Genet. 2010;6:e1000955.
Verpy E, Leibovici M, Zwaenepoel I, Liu XZ, Gal A, Salem N, et al. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nat Genet. 2000;26:51–5.
Chen Q, Zou J, Shen Z, Zhang W, Yang J. Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2. J Biol Chem. 2014;289:36070–88.
Yan J, Pan L, Chen X, Wu L, Zhang M. The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins. Proc Natl Acad Sci USA. 2010;107:4040–5.
Zou J, Zheng T, Ren C, Askew C, Liu X-P, Pan B, et al. Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice. Hum Mol Genet. 2014;23:2374–90.
Kristensen M, Kucharz K, Felipe Alves Fernandes E, Strømgaard K, Schallburg Nielsen M, Cederberg Helms HC, et al. Conjugation of therapeutic PSD-95 inhibitors to the cell-penetrating peptide tat affects blood-brain barrier adherence, uptake, and permeation. Pharmaceutics. 2020;12:661.
Ballarin B, Tymianski M. Discovery and development of NA-1 for the treatment of acute ischemic stroke. Acta Pharmacol Sin. 2018;39:661–8.
Ullmer C, Schmuck K, Figge A, Lübbert H. Cloning and characterization of MUPP1, a novel PDZ domain protein. FEBS Lett. 1998;424:63–8.
Jemth P, Gianni S. PDZ domains: folding and binding. Biochemistry. 2007;46:8701–8.
Hung AY, Sheng M. PDZ domains: structural modules for protein complex assembly. J Biol Chem. 2002;277:5699–702.
Nissen KB, Haugaard-Kedström LM, Wilbek TS, Nielsen LS, Åberg E, Kristensen AS, et al. Targeting protein-protein interactions with trimeric ligands: high affinity inhibitors of the MAGUK protein family. PLoS ONE. 2015;10:e0117668.
Christensen NR, De Luca M, Lever MB, Richner M, Hansen AB, Noes-Holt G, et al. A high-affinity, bivalent PDZ domain inhibitor complexes PICK1 to alleviate neuropathic pain. EMBO Mol Med. 2020;12:e11248.
Rousset R, Fabre S, Desbois C, Bantignies F, Jalinot P. The C-terminus of the HTLV-1 Tax oncoprotein mediates interaction with the PDZ domain of cellular proteins. Oncogene. 1998;16:643–54.
Kiyono T, Hiraiwa A, Fujita M, Hayashi Y, Akiyama T, Ishibashi M. Binding of high-risk human papillomavirus E6 oncoproteins to the human homologue of the Drosophila discs large tumor suppressor protein. Proc Natl Acad Sci USA. 1997;94:11612–6.
Lee SS, Weiss RS, Javier RT. Binding of human virus oncoproteins to hDlg/SAP97, a mammalian homolog of the Drosophila discs large tumor suppressor protein. Proc Natl Acad Sci USA. 1997;94:6670–5.
Awad A, Sar S, Barré R, Cariven C, Marin M, Salles JP, et al. SHIP2 regulates epithelial cell polarity through its lipid product, which binds to Dlg1, a pathway subverted by hepatitis C virus core protein. Mol Biol Cell. 2013;24:2171–85.
Razanskas R, Sasnauskas K. Interaction of hepatitis B virus core protein with human GIPC1. Arch Virol. 2010;155:247–50.
Hsu E-C, Lin Y-C, Hung C-S, Huang C-J, Lee M-Y, Yang S-C, et al. Suppression of hepatitis B viral gene expression by protein-tyrosine phosphatase PTPN3. J Biomed Sci. 2007;14:731–44.
Blot V, Delamarre L, Perugi F, Pham D, Bénichou S, Benarous R, et al. Human Dlg protein binds to the envelope glycoproteins of human T-cell leukemia virus type 1 and regulates envelope mediated cell-cell fusion in T lymphocytes. J Cell Sci. 2004;117:3983–93.
Sun F, Xiao Y, Qu Z. Oncovirus Kaposi sarcoma herpesvirus (KSHV) represses tumor suppressor PDLIM2 to persistently activate nuclear factor κB (NF-κB) and STAT3 transcription factors for tumorigenesis and tumor maintenance. J Biol Chem. 2015;290:7362–8.
Teoh K-T, Siu Y-L, Chan W-L, Schlüter MA, Liu C-J, Peiris JSM, et al. The SARS coronavirus E protein interacts with PALS1 and alters tight junction formation and epithelial morphogenesis. Mol Biol Cell. 2010;21:3838–52.
Ruch TR, Machamer CE. The coronavirus E protein: assembly and beyond. Viruses. 2012;4:363–82.
Jimenez-Guardeño JM, Nieto-Torres JL, DeDiego ML, Regla-Nava JA, Fernandez-Delgado R, Castaño-Rodriguez C, et al. The PDZ-binding motif of severe acute respiratory syndrome coronavirus envelope protein is a determinant of viral pathogenesis. PLoS Pathog. 2014;10:e1004320.
Schoeman D, Fielding BC. Coronavirus envelope protein: current knowledge. Virol J. 2019;16:69.
Caillet-Saguy C, Durbesson F, Rezelj VV, Gogl G, Tran QD, Twizere J-C, et al. Host PDZ-containing proteins targeted by SARS-CoV-2. FEBS J. 2021;288:5148–62.
Li Y, Wei Z, Yan Y, Wan Q, Du Q, Zhang M. Structure of Crumbs tail in complex with the PALS1 PDZ-SH3-GK tandem reveals a highly specific assembly mechanism for the apical Crumbs complex. Proc Natl Acad Sci USA. 2014;111:17444–9.
Roh MH, Fan S, Liu C-J, Margolis B. The Crumbs3-Pals1 complex participates in the establishment of polarity in mammalian epithelial cells. J Cell Sci. 2003;116:2895–906.
Assémat E, Crost E, Ponserre M, Wijnholds J, Le Bivic A, Massey-Harroche D. The multi-PDZ domain protein-1 (MUPP-1) expression regulates cellular levels of the PALS-1/PATJ polarity complex. Exp Cell Res. 2013;319:2514–25.
Chai J, Cai Y, Pang C, Wang L, McSweeney S, Shanklin J, et al. Structural basis for SARS-CoV-2 envelope protein recognition of human cell junction protein PALS1. Nat Commun. 2021;12:3433.
Toto A, Ma S, Malagrinò F, Visconti L, Pagano L, Stromgaard K, et al. Comparing the binding properties of peptides mimicking the Envelope protein of SARS-CoV and SARS-CoV-2 to the PDZ domain of the tight junction-associated PALS1 protein. Protein Sci Publ Protein Soc. 2020;29:2038–42.
Lo Cascio E, Toto A, Babini G, De Maio F, Sanguinetti M, Mordente A, et al. Structural determinants driving the binding process between PDZ domain of wild type human PALS1 protein and SLiM sequences of SARS-CoV E proteins. Comput Struct Biotechnol J. 2021;19:1838–47.
Massimi P, Shai A, Lambert P, Banks L. HPV E6 degradation of p53 and PDZ containing substrates in an E6AP null background. Oncogene. 2008;27:1800–4.
Brimer N, Vande Pol SB. Papillomavirus E6 PDZ interactions can be replaced by repression of p53 to promote episomal human papillomavirus genome maintenance. J Virol. 2014;88:3027–30.
James C, Roberts S. Viral interactions with PDZ domain-containing proteins—an oncogenic trait? Pathogens. 2016;5:8.
Saidu NEB, Filić V, Thomas M, Sarabia-Vega V, Đukić A, Miljković F, et al. PDZ Domain-Containing Protein NHERF-2 Is a Novel Target of Human Papillomavirus 16 (HPV-16) and HPV-18. J Virol. 2019;94:e00663.
Karlsson OA, Ramirez J, Öberg D, Malmqvist T, Engström Å, Friberg M, et al. Design of a PDZbody, a bivalent binder of the E6 protein from human papillomavirus. Sci Rep. 2015;5:9382.
Ramirez J, Poirson J, Foltz C, Chebaro Y, Schrapp M, Meyer A, et al. Targeting the two oncogenic functional sites of the HPV E6 oncoprotein with a high-affinity bivalent ligand. Angew Chem Int Ed Engl. 2015;54:7958–62.
Doyle DA, Lee A, Lewis J, Kim E, Sheng M, MacKinnon R. Crystal structures of a complexed and peptide-free membrane protein-binding domain: molecular basis of peptide recognition by PDZ. Cell. 1996;85:1067–76.
Hill MD, Goyal M, Menon BK, Nogueira RG, McTaggart RA, Demchuk AM, et al. Efficacy and safety of nerinetide for the treatment of acute ischaemic stroke (ESCAPE-NA1): a multicentre, double-blind, randomised controlled trial. Lancet. 2020;395:878–87.
Choi J, Ma S, Kim H-Y, Yun J-H, Heo J-N, Lee W, et al. Identification of small-molecule compounds targeting the dishevelled PDZ domain by virtual screening and binding studies. Bioorg Med Chem. 2016;24:3259–66.
Coluccia A, La Regina G, Naccarato V, Nalli M, Orlando V, Biagioni S, et al. Drug design and synthesis of first in class PDZ1 targeting NHERF1 inhibitors as anticancer agents. ACS Med Chem Lett. 2019;10:499–503.
Hori K, Ajioka K, Goda N, Shindo A, Takagishi M, Tenno T, et al. Discovery of potent disheveled/Dvl inhibitors using virtual screening optimized with NMR-based docking performance index. Front Pharmacol. 2018;9:983.
Chen X, Longgood JC, Michnoff C, Wei S, Frantz DE, Bezprozvanny L. High-throughput screen for small molecule inhibitors of Mint1-PDZ domains. ASSAY Drug Dev Technol. 2007;5:769–84.
Münz M, Hein J, Biggin PC. The role of flexibility and conformational selection in the binding promiscuity of PDZ domains. PLoS Comput Biol. 2012;8:e1002749.
Hill MD, Martin RH, Mikulis D, Wong JH, Silver FL, terBrugge KG, et al. Safety and efficacy of NA-1 in patients with iatrogenic stroke after endovascular aneurysm repair (ENACT): a phase 2, randomised, double-blind, placebo-controlled trial. Lancet Neurol. 2012;11:942–50.
Bach A, Chi CN, Pang GF, Olsen L, Kristensen AS, Jemth P, et al. Design and synthesis of highly potent and plasma-stable dimeric inhibitors of the PSD-95-NMDA receptor interaction. Angew Chem Int Ed. 2009;48:9685–9.
Yang L, Shi P, Zhao G, Xu J, Peng W, Zhang J, et al. Targeting cancer stem cell pathways for cancer therapy. Signal Transduct Target Ther. 2020;5:8.
Shan J, Shi D-L, Wang J, Zheng J. Identification of a specific inhibitor of the dishevelled PDZ domain †. Biochemistry. 2005;44:15495–503.
Shan J, Zhang X, Bao J, Cassell R, Zheng JJ. Synthesis of potent dishevelled PDZ domain inhibitors guided by virtual screening and NMR studies: inhibitors of the dishevelled PDZ domain. Chem Biol Drug Des. 2012;79:376–83.
Lee H-J, Wang NX, Shi D-L, Zheng JJ. Sulindac inhibits canonical Wnt signaling by blocking the PDZ domain of the protein dishevelled. Angew Chem Int Ed. 2009;48:6448–52.
Kim H, Choi S, Yoon J, Lim HJ, Lee H, Choi J, et al. Small molecule inhibitors of the Dishevelled- CXXC 5 interaction are new drug candidates for bone anabolic osteoporosis therapy. EMBO Mol Med. 2016;8:375–87.
Mayasundari A, Ferreira AM, He L, Mahindroo N, Bashford D, Fujii N. Rational design of the first small-molecule antagonists of NHERF1/EBP50 PDZ domains. Bioorg Med Chem Lett. 2008;18:942–5.
Kamdem N, Roske Y, Kovalskyy D, Platonov MO, Balinskyi O, Kreuchwig A, et al. Small-molecule inhibitors of the PDZ domain of Dishevelled proteins interrupt Wnt signalling. Magn Reson. 2021;2:355–74.
Fujii N, Haresco JJ, Novak KAP, Stokoe D, Kuntz ID, Guy RK. A selective irreversible inhibitor targeting a PDZ protein interaction domain. J Am Chem Soc. 2003;125:12074–5.
Stiffler MA, Chen JR, Grantcharova VP, Lei Y, Fuchs D, Allen JE, et al. PDZ domain binding selectivity is optimized across the mouse proteome. Science. 2007;317:364–9.
Shao X, Zhu L, Wang Y, Lu Y, Wang W, Zhu J, et al. Threonine 82 at the PDZ domain of PICK1 is critical for AMPA receptor interaction and localization. Neurochem Int. 2010;56:962–70.
Haugaard-Kedström LM, Clemmensen LS, Sereikaite V, Jin Z, Fernandes EFA, Wind B, et al. A high-affinity peptide ligand targeting syntenin inhibits glioblastoma. J Med Chem. 2021;64:1423–34.
Work partly supported by grants from the Italian Ministero dell’Istruzione dell’Universita ‘ e della Ricerca (Progetto di Interesse ‘Invecchiamento’ to S.G.), Sapienza University of Rome (RP11715C34AEAC9B and RM1181641C2C24B9, RM11916B414C897E to S.G.), the Associazione Italiana per la Ricerca sul Cancro (Individual Grant – IG 24551 to S.G.) the Istituto Pasteur Italia (Teresa Ariaudo Research Project 2018, to A.T.). F.M. was supported by a fellowship from the FIRC—Associazione Italiana per la Ricerca sul Cancro (Filomena Todini fellowship). R.S. is grateful to AIRC, IG 2020, code n. 24703, and Sapienza University of Rome (RM120172A7EAD07C), and G.L.R. to Istituto Pasteur Italia—Fondazione Cenci Bolognetti (Call 2019, under 45) and Sapienza University of Rome (RP11715C7D1CF0D1 and RM11916B5598E3C4) for financial support.
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Nardella, C., Visconti, L., Malagrinò, F. et al. Targeting PDZ domains as potential treatment for viral infections, neurodegeneration and cancer. Biol Direct 16, 15 (2021). https://doi.org/10.1186/s13062-021-00303-9
- Small molecules
- Protein–protein interactions