Structural and functional characterization of the PDZ domain of the human phosphatase PTPN3 and its interaction with the human papillomavirus E6 oncoprotein.

The human protein tyrosine phosphatase non-receptor type 3 (PTPN3) is a PDZ (PSD-95/Dlg/ZO-1) domain-containing phosphatase with a tumor-suppressive or a tumor-promoting role in many cancers. Interestingly, the high-risk genital human papillomavirus (HPV) types 16 and 18 target the PDZ domain of PTPN3. The presence of a PDZ binding motif (PBM) on E6 confers interaction with a number of different cellular PDZ domain-containing proteins and is a marker of high oncogenic potential. Here, we report the molecular basis of interaction between the PDZ domain of PTPN3 and the PBM of the HPV E6 protein. We combined biophysical, NMR and X-ray experiments to investigate the structural and functional properties of the PDZ domain of PTPN3. We showed that the C-terminal sequences from viral proteins encompassing a PBM interact with PTPN3-PDZ with similar affinities to the endogenous PTPN3 ligand MAP kinase p38γ. PBM binding stabilizes the PDZ domain of PTPN3. We solved the X-ray structure of the PDZ domain of PTPN3 in complex with the PBM of the HPV E6 protein. The crystal structure and the NMR chemical shift mapping of the PTPN3-PDZ/peptide complex allowed us to pinpoint the main structural determinants of recognition of the C-terminal sequence of the E6 protein and the long-range perturbations induced upon PBM binding.

The E6 proteins of HPV16 and HPV18 possess a conserved C-terminal PDZ binding motif (PBM), which mediates interaction with some cellular PDZ domain-containing proteins. The ability of E6 to bind to PDZ domain-containing proteins correlates with its oncogenic potential 6 . The PDZ domain of PTPN3 (PTPN3-PDZ) has been identified as a target of the E6 PBM of HPV16 and 18. This PDZ-PBM interaction results in the ubiquitin-mediated proteasomal degradation of PTPN3. Therefore, the endogenous levels of PTPN3 are particularly low in HPV-positive cervical carcinoma cell lines 3 .
To date, the structure of PTPN3-PDZ is not known and the PDZ-mediated interactions between PTPN3 and viral partners have not been described. Indeed, the few biophysical and structural studies on PTPN3 have focused on the PTP domain in complex with phospho-peptide substrates derived either from the mitogen-activated protein kinase (MAPK) p38γ (also known as MAPK12) 7 or the Epidermal growth factor receptor substrate 15 (Eps15) 8 . We have previously shown that the PDZ domain of the closely related PTPN4 inhibits its phosphatase activity 9,10 . Similarly, the inhibitory role of the PDZ domain of PTPN3 on the catalytic activity has been reported using a phospho-p38γ peptide as a substrate for kinetics experiments 7 .
In this study, we report the structural and functional analyses of the PDZ domain of PTPN3. We investigated the molecular mechanism of interaction between the PDZ domain of PTPN3 and the PBM of cellular and viral partners (Table 1), the MAP kinase p38γ, the HBV core protein and the HPV E6 protein. We employed an integrative approach based on biophysical, nuclear magnetic resonance (NMR) and X-ray crystallography experiments. We showed that the C-terminal PBM sequences of the HPV E6 protein interact with PTPN3-PDZ with similar affinities to those of the endogenous PTPN3 ligand p38γ and the HBV Core protein 4 . By solving the X-ray structure and mapping the NMR chemical shift changes of PTPN3-PDZ in complex with the PBM of HPV16 E6, we identified the molecular basis of recognition of the C-terminal sequence of E6 protein and the induced perturbations that spread from the binding groove.

Results
Quality control of the recombinant PTPN3-PDZ domain. Presently, there is no structural information on PTPN3-PDZ other than that provided by homology modelling 7 . To bridge this gap, we performed different structural and biophysical studies on the recombinant PTPN3-PDZ construct ( Fig. 1)

expressed in Escherichia coli.
To estimate the secondary structure content of the PDZ construct, we performed circular dichroism (CD) measurements in the far-UV (195-240 nm). The PTPN3-PDZ spectrum ( Fig. 2A) appeared to be of mixed α-helix and β-sheet content, which upon deconvolution indicated 16% α-helix and 32% β-sheet. The secondary structure content extracted from the X-ray structure of the PDZ domain of its close homologue PTPN4 (PTPN4-PDZ) (PDB id 3NFK) 11 is 17% α-helix and 31% β-sheet. Thus, the PTPN3-PDZ construct presents a secondary structure content similar to that of PTPN4-PDZ.
We assessed the tertiary folding of PTPN3-PDZ by NMR by performing 15  Stability and oligomeric state of PTPN3-PDZ. To evaluate the stability of PTPN3-PDZ, we performed differential scanning calorimetry (DSC) (Fig. 2C). A single endothermic peak was observed in the DSC thermogram, with a thermal transition midpoint (T m ) of 41 °C. As a comparison, we performed DSC on PTPN4-PDZ. We obtained an endothermic peak with a T m of 47 °C (Fig. 2C). The data show that PTPN3-PDZ is less stable in Figure 1. Schematic representation of the PTPN3 constructs. Numbers on both extremities indicate the boundary residues for each construct; Numbers in italic above the schematic construct of full-length PTPN3 correspond to the boundary residues of each protein domain from Uniprot P26045. www.nature.com/scientificreports www.nature.com/scientificreports/ solution than PTPN4-PDZ. This thermal instability of the PTPN3-PDZ construct could be responsible for its aggregation previously detected by NMR. Indeed, we observed a significant loss of peak intensities in the HSQC spectrum of PTPN3-PDZ related to aggregation after 10 h at 20 °C (data not shown).

Peptides
To estimate the oligomeric state of the PTPN3-PDZ construct, analytical ultracentrifugation (AUC) experiments were performed (Table 2). Three different concentrations of the protein were tested, 10, 25 and 70 μM. Only one single peak was detected at 10 μM with a sedimentation coefficient of 1.5S in agreement with a monomeric form of 10.5 kDa. At 25 μM, an additional peak was detected with a sedimentation coefficient of 2.6S corresponding to a dimeric form. At a concentration of 70 μM, higher oligomeric species could be detected. Thus, the AUC data of the PTPN3-PDZ construct reveal a concentration-dependent equilibrium between monomer, dimer and higher oligomeric states with only monomers detected at a concentration of 10 μM.  15 N HSQC spectra of PTPN3-PDZ (black) and PTPN3-PDZ Next (red). (C) DSC thermograms of PTPN3-PDZ unbound and complexed to PBM peptides. Free PTPN3-PDZ curve is shown as a black line, and PTPN3-PDZ complexed to p38γ PBM, HBVc PBM and HPV16E6 PBM and HPV18E6 PBM curves are shown as yellow, purple, green and red lines, respectively. The DSC thermogram of free PTPN4-PDZ is colored in blue. (D) Sedimentation coefficient distributions of PTPN3-PDZ Next unbound and complexed to viral PBM peptides. The black, red, green and purple lines correspond to PTPN3-PDZ Next unbound and complexed to HPV18E6PBM, HPV16E6 PBM and HBVc PBM, respectively.  www.nature.com/scientificreports www.nature.com/scientificreports/ PBM-mediated stabilization of the PTPN3-PDZ. To check whether the PBM binding to the PDZ domain could affect the stability of PTPN3-PDZ, we performed DSC and AUC on PTPN3-PDZ in complex with the p38γ PBM and the viral PBMs of HBV Core and HPV 16 and 18 E6 proteins, namely HBVc PBM, HPV16E6 PBM and HPV18E6 PBM respectively (Table 1). These PBMs have been shown to interact with the PTPN3-PDZ 3,4,7 . A single endothermic peak was observed in the DSC thermograms of all complexes (Fig. 2C) with a Tm of 45 °C, 47 °C, 52 °C and 49 °C for PTPN3-PDZ complexed to p38γ PBM, HBVc PBM, HPV16E6 PBM and HPV18E6 PBM, respectively (Table 1). For all the PBMs tested, an increase of 4 to 11 °C in the Tm was observed, showing that the PBM binding onto PTPN3-PDZ stabilizes the domain, whether the PBM is of cellular or viral origin.
In addition, AUC experiments of the PTPN3-PDZ construct at 70 μM complexed to HBVc PBM show only one species with a sedimentation coefficient of 1.6S corresponding to a one-to-one complex with the peptide, without higher oligomeric species (Table 2). Thus, the PBM binding onto PTPN3-PDZ prevents oligomerization at high concentration.
Affinities of the viral and the cellular PBMs for PTPN3-PDZ. The affinities of HPV16E6 PBM, HPV18E6 PBM, p38γ PBM and HBVc PBM for PTPN3-PDZ were measured by NMR titration. We followed 1 H, 15 N chemical shift perturbations of PTPN3-PDZ signals in the 1 H-15 N HSQC spectra as a function of increasing concentrations of the PBM peptide to determine the dissociation constant (K D ) (Fig. S1). The p38γ PBM peptide binds to PTPN3-PDZ with a K D value of 26 μM (Table 1). This affinity is 16-fold lower than the one previously reported for PTPN4-PDZ (K D of 1.6 μM) 10 . We obtained K D values of 29 μM, 53 μM and 37 μM for PTPN3-PDZ with HBVc PBM, HPV16E6 PBM and HPV18E6 PBM, respectively ( Table 1). The K D values are all in the same tenth-of-micromolar range for the viral PBMs and are close to the one of the cellular partner p38γ. The measured affinities fall in the standard 0.1-100 μM range 12 for PDZ-PBM interactions. To rule out the possibility of an effect of self-association of PTPN3-PDZ on the K D values, we compared the K D values with the HPV16E6 and HPV18E6 PBM peptides fitted from the NMR data with the ones estimated from the binding intensities (BIs) obtained for the HPV16E6 and HPV18E6 PBM peptides measured from a quantitative screening assay against the human PDZome library, in which each PDZ domain is at a concentration of 4 μM and in excess of PBM peptides 12 . The BIs are directly related to the Kd. For PTPN3-PDZ, the estimated K D values are 46 and 96 μM for the HPV16E6 and HPV18E6 PBMs respectively, in good agreement with our experimental results.
Stabilization of PTPN3-PDZ for structural studies. The instability and tendency to oligomerize of PTPN3-PDZ made this construct unsuitable for crystallogenesis. To gain in stability and protein expression yield, we extended the N-terminal extremity of PTPN3-PDZ by 15-residues with its wild-type upstream sequence (PTPN3-PDZ Next in Fig. 1). These extensions have been reported to provide structural stability to some PDZ containing proteins 13,14 . The PTPN3-PDZ production yield was increased two-fold after extension from 0.9 mg to 1.8 mg of purified protein per liter of culture. The stability of PTPN3-PDZ Next was then evaluated by NMR HSQC spectra recorded during a week at 20 °C. Spectra show a similar pattern of resonances than in the HSQC spectrum of PTPN3-PDZ without any signs of aggregation, such as a loss of peak intensity (Fig. 2B). The additional peaks of the N-terminal extension residues fall in the spectral region characteristic of unfolded protein and no chemical shift differences between PTPN3-PDZ Next and the shorter form are detected. Thus, the N-terminal extension is not structured in the PTPN3-PDZ Next and does not interact with the PDZ domain.
In addition, one single peak was detected by AUC for PTPN3-PDZ Next at concentrations between 17.5 μM and 70 μM with a sedimentation coefficient of 1.6-1.7S, in agreement with a monomeric form of 12.7 kDa ( Table 2) and devoid of higher oligomeric species. All these data indicate that the extension of PTPN3-PDZ resulted in a stable and folded PDZ domain in solution.
AUC experiments were also performed on the PTPN3-PDZ Next construct at 70 μM complexed to HBVc PBM, HPV16E6 PBM and HPV18E6 PBM ( Table 2 and Fig. 2D). As expected, only one species with a sedimentation coefficient of 1.6S is detected in all cases, corresponding to a one-to-one complex.

Crystal structure of the PDZ domain of PTPN3 in complex with the viral HPV16E6 PBM.
To investigate the molecular determinants of the interaction of PTPN3 with the HPV16 E6 protein, we solved the crystal structure of the complex formed by PTPN3-PDZ Next and HPV16E6 PBM by molecular replacement at 2.19 Å resolution ( Table 3). The structure factors and coordinates have been deposited in the Protein data Bank under accession code 6HKS.
PTPN3-PDZ Next adopts a typical PDZ fold, with a β-sandwich comprising five β strands and two α helices (Fig. 3A). The PBM ligand binds in a hydrophobic cleft formed by the β2-strand, the α2-helix and the "GLGF" loop (Figs 3A,B). HPV16E6 PBM binds to the PDZ domain as an anti-parallel extension of the β2-strand domain in a conventional mode. There is no electron density corresponding to the N-terminal extension of PTPN3-PDZ Next in the crystal, which indicates a disordered region, in agreement with the NMR results that show an unfolded extension.
We also determined a 3D structural model with the CS-ROSETTA approach 15 using the 15 N, 13 C α , 13 CO NMR backbone and 13 C β resonances of PTPN3-PDZ Next complexed to HPV16E6 PBM (BMRB accession number 27645). The CS-Rosetta modeling using solution NMR data revealed a very similar conformation to the crystal structure, with a low root mean square deviation (rmsd) of 1.11 Å for the backbone atoms between the crystal structure and the averaged solution model originated from the 10 lowest energy models (Fig. 4C). Thus, 3D models of PDZ-PTPN3 determined by CS-Rosetta reveal a conformation in solution that matches the crystal structure of the PDZ domain of the complex PTPN3-PDZ Next and HPV16E6 PBM (Fig. 3B). The AUC sedimentation velocity was also back-calculated using the crystal structure 16 . We obtained a calculated sedimentation coefficient value www.nature.com/scientificreports www.nature.com/scientificreports/ of 1.59S, which is in good agreement with the experimental measurement of 1.6S. Thus, the overall structure of the domain in the crystal is consistent with its arrangement observed in solution.
Then, we compared the PDZ domains of PTPN3 and PTPN4, which share 71% of sequence identity (Fig. 4A). Both structures of PTPN3-PDZ and PTPN4-PDZ are highly similar, with a very low rmsd value of 0.34 Å for the backbone atoms (PTPN4 PDB ID 5EYZ) 10 (Fig. 4B).

Structural insights on the recognition of the PBM of HPV16 E6 protein.
The PDZ domain of PTPN3 possesses the interaction network specific to class I PDZ domains and recognizes the consensus sequence S/T-X-Φ COOH , where X is any residue, and Φ is a hydrophobic residue 17 . A clear electron density map was seen for only the last seven C-terminal residues of HPV16E6 PBM (-TRRETQL COOH ) that are inserted into the binding groove (Fig. 3A,B). Similarly, only the last 5 or 6 C-terminal residues of PBM peptides are visible in the crystal PTPN4-PDZ structures in complex with PBM peptides (PDB IDs 3NFL, 3NFK, 5EZO, 5EYZ in references 10,11 ).
The interactions of the PBM residues at positions 0 and −2 with PTPN3-PDZ are quite similar to the bonding patterns already observed in the complex between PDZ-PTPN4 and the viral peptide Cyto13-att (-GETRL -COOH ) derived from the attenuated rabies virus, or the optimized pro-apoptotic 13-amino acids peptide Cyto8-RETEV (-RETEV -COOH ) (PDB IDs 3NFK and 5EYZ respectively) 10,11 . Indeed, the C-terminal carboxylate of the leucine (L 0 ) of the HPV16E6 PBM forms three H-bonds with the amide nitrogens of F521, G522 and F523 of the "GLGF motif " on PTPN3-PDZ (Fig. 3B) as observed for F528, G529 and F530 of PTPN4-PDZ with the L 0 of the Cyto13-att (-GETRL -COOH ) PBM 11 . The hydroxyl group of threonine at position −2 forms a hydrogen bond with the Nε2 of the conserved histidine H572 from the α2-helix of PTPN3-PDZ (Fig. 3B). Electron acceptors such as serine and threonine are therefore preferred at this position for the class I PDZ domains.
At position −1 of HPV16E6 PBM, the glutamine (Q −1 ) side chain well defined and forms a H-bond with a water molecule that is also H-bonded to the Nδ2 of N524 of PTPN3-PDZ (Fig. 3B), whereas it is exposed to the solvent. Interestingly, in the complex of PTPN4-PDZ with the PBM of the glutamate receptor subunit GluN2A (PDB ID 3NFL), which presents a D in position −1 11 , the D −1 forms a H-bond with the N531 side-chain amine group of PTPN4-PDZ, the equivalent of N524 of PTPN3-PDZ.
A glutamate at position −3 (E −3 ) is conserved in all viral PBMs targeting PTPN3 and is also present in the one of p38γ. The side-chain carboxyl of E −3 forms a bifurcated H-bond with the hydroxyl of the conserved S538 (S545 for PTPN4) and N524 (N531 for PTPN4) amine group (Figs 3B and 4A). E −3 is also stabilized by hydrophobic contacts involving its Cβ-Cγ carbon chain and the long aliphatic side chain of K526 as observed in PTPN4 (K533) bound to Cyto8retev (PDB 5EYZ).
Finally, the guanidinium nitrogens of arginine at position −4 (R −4 ) form ionic bonds with the carboxylate oxygens of D573 (D580 in PTPN4) (Fig. 3B).  www.nature.com/scientificreports www.nature.com/scientificreports/ To determine short-and long-range perturbations in PTPN3-PDZ upon PBM binding, we analyzed by solution NMR the chemical shifts of the free PTPN3-PDZ in solution and its complex with peptide HPV16E6 PBM, comparing their 1 H, 15 N HSQC spectra. We assigned 97% of the HN resonances, 99% of the Cα resonances, 90% of the Cβ resonances and 89% of the CO resonances (89 non-Proline residues over 94) of PTPN3-PDZ complexed to HPV16E6 PBM (BMRB accession number 27645). Chemical shift changes (Δδ) in PTPN3-PDZ spectra upon complex formation provide insights at atomic level on the residues involved in the interaction with the HPV16E6 PBM and on potential distal effects. Two types of signals were useful for the analysis of the 1 H, 15 N chemical shift mapping (Fig. 5A): (1) signals experiencing significant chemical shift changes (Δδ > 0.15 ppm); (2) signals that undoubtedly disappear from their original well-resolved position in the spectrum upon complex formation and are therefore severely affected when binding to the PBM (either due to large chemical shift changes or to severe line broadening effects caused by exchange). Residues corresponding to type 1 are shown in blue in Fig. 5A,B, while seven residues of type 2 are colored in red. Nine residues, whose behavior could not be safely defined mainly because they fall in crowded spectral regions, are colored in gray.
As expected, we identified differences in backbone NH chemical shifts between free PTPN3-PDZ and when bound to HPV16E6 PBM. Residues G522, G527 and H572, are among the most affected and are located in the PBM binding site. I559 and L590 also experience a strong effect. Indeed, they make hydrophobic contacts of 5.4 Å and 4 Å with F523 and F521 of the "GLGF motif ", respectively. E589 (in red), the direct neighbor of L590, displays perturbations both in chemical shift or intensity. Some residues of α2-helix in the binding site are affected: D573 and F578 (in blue) and V575 (in red). We find also residues such as F521 and F523 of the "GLGF" motif and D516 in the "GLGF" loop affected in their NMR resonances. D530 in the β2-β3 loop forms a H-bond with H572, which interacts directly with the PBM peptide (position T −2 ).
Interestingly, G556 (in red) is part of a path of perturbation starting from G527 (in red) and G528 (in blue) at the end of β2-strand in the binding groove, transmitted to the close V536 (in red) at the beginning of β3-strand, affected www.nature.com/scientificreports www.nature.com/scientificreports/ in signal intensity. The perturbation of V536 seems to be transferred to the close G556 on the β4-strand. I559 (in red) on β4-strand is also affected, possibly experiencing the perturbation of the F523 located 5 Å away of the "GLGF motif ". Finally, the path of perturbation finishes with R595 at the C-terminus of the PDZ domain (in blue). Thus, long-range perturbations seem to be induced upon PBM binding and transmitted through an interconnected network of residues throughout PTPN3-PDZ. This network involves the β2, β3 and β4 strands and the C-terminus.

Discussion
PTPN3 is a PDZ domain-containing phosphatase that has been demonstrated to function as a tumor suppressor or, conversely, as an oncoprotein in a context-dependent manner. It integrates a number of signaling pathways via interactions mediated by its PDZ domain [18][19][20] . The PDZ domain of PTPN3 is also a cellular target of oncoviruses. Until now, no structural data on this domain were available. We investigated the structural and functional properties of PTPN3-PDZ and characterized its interaction with the PBMs of one cellular partner, the MAP kinase p38γ, and of its viral partners, the HPV E6 protein and the HBV core protein. We defined in particular the molecular basis of the PDZ-PBM interaction between HPV E6 and PTPN3.
Structural properties of the PDZ domain of PTPN3. The crystal structure of PTPN3-PDZ Next complexed to HPV16E6 PBM reveals a typical PDZ fold with five β-strands and two α-helices (Fig. 3A,B). It was previously reported that some PDZ domains can be stabilized by extensions of either the N-, C-, or both termini of a PDZ 21 . These extended regions were required for correct folding and ligand binding. For example, the PDZ1 of the membrane-associated guanylate kinase inverted MAGI-1 is unstable without N-and C-terminal extensions of 14 and 26 residues, respectively, even though these sequences are unstructured in both free and ligand-bound states 22 . Our minimal PTPN3-PDZ construct, deduced from sequence alignments with PDZ domains of known structure (Fig. 1), started at residue 504, while the first N-terminal secondary structure element observed in the crystal structure of PTPN3-PDZ Next , the β1-strand, started at residue 507 and not at 510 as expected from the sequence alignments. We showed that this PTPN3-PDZ construct is folded but unstable. We were able to increase its stability and production yield, while decreasing its tendency to auto-associate, by the addition of an unfolded 15-residue N-terminal extension to the minimal delimitation of PTPN3-PDZ. 3D structural models of PDZ-PTPN3 in complex with HPV16E6 PBM determined by CS-Rosetta using backbone and 13 C β NMR chemical shift assignments revealed a conformation in solution congruent with the X-ray structure of the PDZ domain.
Our AUC data showed that PTPN3-PDZ auto-association is prevented by PBM binding, as already reported for other PDZ domains 23 . The molecular mechanism by which PBM binding interferes with PTPN3 PDZ auto-association remains unknown. Our NMR results on long-range perturbations upon PBM binding are consistent with a network involving the β2, β3 and β4 strands and the C-terminus residues throughout PTPN3-PDZ. This connected pathway communicates the binding event to regions that are distal to the binding cleft. These findings are compatible with previous data on PDZ domains suggesting that energetic pathways within PDZ domains may support allostery [24][25][26][27] . A regulation controlled by the equilibrium between PBM binding and dimerization is attractive since over 30% of PDZ domains are known to form dimers in solution 28 . www.nature.com/scientificreports www.nature.com/scientificreports/ The PDZ domain of PTPN3 as a target of viruses. We showed that the viral PBMs interact with PTPN3-PDZ with similar affinities to that of the endogenous PTPN3 ligand p38γ. Despite variations in the PBM sequences, all the affinities fall in the 25-55 μM range (Table 1), in agreement with affinities previously reported for HPV E6 PBM PDZ binders 12 . This result is consistent with the hypothesis of a competition between cellular PBM-containing partners and PBMs on viral proteins to bind PTPN3 and hijack signalling pathways in infected cells. E6 binding to PTPN3 should be favoured in HPV infected cells since E6 is highly expressed in HPV-derived cancer cells. Only the C-termini of E6 oncoproteins in high-risk HPV strains contain PBMs, and this is a marker of high oncogenic potential. The presence of a PBM on E6 confers the capacity to interact with various cellular PDZ domain-containing proteins including PTPN3 29 . Furthermore, this interaction causes degradation of most of its targets through the ubiquitin-proteasome pathway 30 . Therefore, PDZ-protein interactions with E6 PBM not only disrupt protein-protein interactions but also promote degradation of the PDZ-containing protein. Our results raise the question of how specificity is achieved in this interaction, and whether or not PTPN3 PDZ domain is able to discriminate its binding partners.

Molecular basis and specificities of the interaction with the PDZ domain of PTPN3. The crystal
structure and the NMR chemical shift mapping of PDZ-PTPN3 in complex with the PBM of the E6 oncogenic protein of HPV16 highlight the main structural determinants of recognition of the C-terminal sequence of the E6 protein. HPV16E6 PBM binding to PTPN3-PDZ is consistent with the binding mode observed for canonical class I PDZ domains, where L 0 and T −2 are involved in key interactions with the PDZ domain. Indeed, L 0 interacts with the conserved GLGF motif, which is crucial for the hydrogen bond coordination of the terminal carboxylate group during the PDZ domain-PBM ligand interaction. Moreover, the T −2 forms a hydrogen bond with a conserved Histidine or Arginine in the PDZ domain, signature of class I PDZ domains 14,31 . The histidine, H572 in PTPN3, is very well conserved in the PTPN3 and PTPN4 orthologs (Fig. 6), and was also identified as a preferred www.nature.com/scientificreports www.nature.com/scientificreports/ residue for E6 binding by the alignment of 209 PDZ domains ranked according to their highest E6 binding intensity, as determined by a high-throughput assay 12 .
At position −1 of HPV16E6 PBM, a glutamine forms a H-bond with a water molecule that is also H-bonded to the N524 of the PDZ domain of PTPN3, whereas the N531 of PTPN4 forms a H-bond with the D in position −1 in the PBM of the cellular partner GluN2A-16 11 . This asparagine is very well conserved in the orthologs of PTPN3 and PTPN4, while a serine or threonine is more commonly found at this position in the PDZome.
N524 and S538 (S545 for PTPN4) form also H-bonds with the E in position −3 of the HPV16E6 PBM (Figs 3B and 4A). S538 and N524 are strictly conserved in PTPN3 and PTPN4 orthologues, with only 2 and 1 exceptions respectively (Fig. 6); although in the PDZome, S or T residues are often located at this position 524, and in position 538, we often find S or T but also K, H, Q and R. E −3 is also stabilized by K526 in PTPN3. This K is conserved in PTPN3 and PTPN4 orthologues but only a few K are present at this position in the human PDZome and I, V, A, S and M are more often found. We previously reported that one single mutation (Q to E) at position −3 of the PBM of the envelope G protein of rabies virus (RABV) switches the fate of the infected cell from survival to apoptosis 32 . Indeed, the Q to E change increases the number and change the pattern of cellular partners for the PBM in the infected cells, enabling the attenuated RABV strain G protein to interact with PTPN4 inducing cell death. PTPN4-PDZ is able to discriminate between these peptides, displaying a substantially higher affinity for E rather than Q in position −3. Altogether, these observations and the fact that a glutamic acid is often found in position −3 in all PBMs interacting with PTPN3 and PTPN4 3,4,10,11,19,20,32,33 suggest that interactions with this E in position −3 are a critical determinant of specificity of PDZ/PBM interaction in the NT5 group comprising PTPN3 and PTPN4 phosphatases.
Finally, the arginine in position −4 is linked by ionic bonds to D573 in PTPN3-PDZ (D580 in PTPN4-PDZ) complexed to HPV16E6 PBM. This interaction is most likely maintained in the complexes with viral HPV18E6 PBM, HBVc PBMs, and even with the p38γ PBM, which presents a lysine instead of an arginine. D573 is well conserved in the orthologous PTPN3 and PTPN4 with only 3 exceptions, yet it is not the most frequently found amino acid at this position in the human PDZome. It might also be a specificity determinant common to the PDZ of PTPN3 and PTPN4 phosphatases. These two closely-related non-receptor PTPs that compose the NT5 subfamily emerged in holozoa 34 and duplicated in vertebrates with 54% of sequence identity, which rises to 71% for their PDZ domains. However, the expression pattern, substrates and interacting partners of PTPN3 and PTPN4 have a limited overlap.

Methods
Production and purification of recombinant proteins and PBM ligands. PTPN3-PDZ and PTPN3-PDZ Next (Fig. 1) are encoded as an N-terminal gluthathione S-transferase (GST) tagged protein in a pDEST15 expression plasmid and a pGST//2 (derived from pGEX-4T-1; Amersham) expression plasmid respectively. A TEV cleavage site is introduced between the N-terminal tag and the protein sequence. The vectors were used to transform E. coli BL21 Star (DE3) star cells (Invitrogen, Carlsbad, CA, USA). Uniformly 15 N-labeled, 13 C, 15 N-labeled and unlabeled PTPN3-PDZ and PTPN3-PDZ Next constructs were expressed and purified as previously described 9 .
Briefly, harvested cells were resuspended in buffer A (50 mM Tris/HCl, pH 7.5, 150 mM NaCl), 2 mM β-mercaptoethanol and protease inhibitor cocktail (Roche), and then disrupted in a French press. The clarified supernatants were loaded onto a GST column (GSTrap HP, GE Healthcare) and washed with the same buffer. The GST tag was cleaved by overnight incubation at 4 °C by TEV protease (1% mol/mol) directly injected into the column. The eluted fractions containing the protein were pooled and loaded onto a size exclusion column (HiLoad Superdex 75 pg; GE) equilibrated with buffer A with 0.5 mM Tris(2-carboxyethyl)phosphine (TCEP). For crystallogenesis of PTPN3-PDZ Next , the same protocol was followed, replacing the Tris/HCl in buffer A by 20 mM HEPES pH 8 on the size exclusion chromatography step. Purified proteins were concentrated using centrifugal filter devices (Vivaspin, Sartorius). Protein concentration was estimated from its absorbance at 280 nm.
The peptides, p38γ PBM, HBVc PBM, HPV16E6 PBM and HPV18E6 PBM, were synthesized in solid phase using Fmoc strategy (Proteogenix) and resuspended in H 2 O. CD experiments. All CD measurements were acquired with an Aviv 215 spectropolarimeter. Far-UV (195-240 nm) spectra were recorded at 25 °C on 8.4 μM PTPN3-PDZ samples in a cylindrical cell with a 0.2-mm pathlength. Ellipticity was measured every 1 nm. The final spectrum of the protein sample was obtained by averaging three successive scans and subtracting the baseline spectrum of the buffer recorded under the same conditions. The CONTIN program was used for quantitative decomposition of the far-UV CD spectrum 35 .
NMR experiments. The NMR samples for the PTPN3-PDZ and PTPN3-PDZ Next constructs were prepared in buffer A with 0.5 mM TCEP and D 2 O (5-10% vol:vol). All NMR experiments were performed on a 600-MHz Varian NMR System spectrometer equipped with a triple resonance 1 H{ 13 C/ 15 N} cryoprobe.
The NMR titration experiments to measure PTPN3-PDZ·PBM peptide affinities and the NMR experiments for backbone assignment of PTPN3-PDZ in complex with HPV16E6 PBM were performed with the PTPN3-PDZ construct at 15 °C. Briefly, the unlabeled peptides (stock solutions ranging from 2.8 to 5.7 mM) at pH 7.5 were added stepwise in a sample initially containing 240-260 μL of 15 N-labeled PTPN3-PDZ at a concentration of 95 or 149 μM. A series of 1 H, 15 N HSQC spectra was recorded for the different titration points. Chemical shift changes were calculated using the free PTPN3-PDZ signals as a reference. Chemical shift differences in the cross-peaks by titration were calculated using the relationship: Δδ = ((Δδ HN ) 2 + (0. 15 × Δδ N ) 2 ) 0.5 where Δδ HN and Δδ N are changes in the 1 H and 15 N chemical shifts in ppm, respectively. The weighting factor of 0.15 was used to adjust the relative magnitudes of the amide nitrogen chemical shift range and the amide proton chemical shift range. Signals broaden in the moderate fast-exchange regime observed with PTPN3-PDZ and the PBM peptides, increasing the experimental errors on the chemical shift measurements used for the fitting of the Kd. The following of chemical shift changes during titrations and the fitting of curves were performed with the CcpNmr Analysis software 36 . A pool of 8 to 14 peaks with the best fit for each titration were kept to deduce the K D , and the errors are the standard deviations of all the K D values fitted from the curves.
The sequence specific 1 H N , 15 N, 13 C α , 13 C β and 13 CO resonance assignments were performed using TROSY-based versions of the following experiments: 2D 1 H, 15 N HSQC and 3D HNCO, HNCA, HN(CO)CA, CBCA(CO)NH and HNCACB. The spectra were processed with NMRPipe 37 and subsequently analysed in CcpNmr Analysis software 36  AUC experiments. Sedimentation velocity experiments were carried out at 20 °C using a Beckman Coulter XL-I centrifuge equipped with a AN60-Ti rotor. Various protein and protein-peptide complex concentrations (protein concentrations ranging from 12.5 to 70 μM) samples were centrifuged for 17 h at 42000 rpm. Data were analyzed with SEDFIT 15.1 using a continuous size distribution c(S) model. The partial specific volume, the viscosity and the density of the samples were calculated with SEDNTERP. The processed data were used to obtain values of sedimentation coefficients at null concentration in our experimental conditions (S0) and to get the standard sedimentation coefficients in water at 20 °C (S 0,w,20 ) (Table 2). www.nature.com/scientificreports www.nature.com/scientificreports/ Crystallisation, data collection, and structure determination. The HPV16E6 PBM peptide used for co-crystallization was added in excess to form >95% of the complex with the protein. The PDZ domain-peptide complex for crystallization was generated by mixing PTPN3-PDZ Next and the peptide at a ratio of 1:2. Initial screening of crystallization conditions was carried out by the vapor diffusion method using a MosquitoTM nanoliter-dispensing system (TTP Labtech). Sitting drops were set up using 400 nL of a 1:1 mixture of each sample protein and crystallization solutions (672 different commercially available conditions) equilibrated against a 150 μL reservoir in multiwell plates (Greiner Bio-One). The crystallization plates were stored at 4 °C in a RockImager1000 ® (Formulatrix) automated imaging system to monitor crystal growth. The best crystals were obtained by mixing 200 nL of PTPN3-PDZ Next · HPV16E6 PBM complex solution (concentration of the PDZ domain at 4.8 mg/mL) in 20 mM HEPES pH 8, 150 mM NaCl, 0.5 mM TCEP mixed with 200 nL of reservoir solution containing 20% w/v PEG 3350, 0.2 mM KI at pH 7. Crystals were then flash-cooled in liquid nitrogen using Paratone-paraffin 50%(V/V)/50%V/V) oil as the cryoprotectant.
X-ray diffraction data were collected at a wavelength of 0.979 Å on the beamline PROXIMA-2A at Synchrotron SOLEIL (St. Aubin, France). The data were processed with XDS 38 and Xdsme 39 , and other programs from the CCP4 suite 40 . The structures were solved by molecular replacement with PHASER 41 using the search atomic model of PTPN4-PDZ (PDB ID 5EZ0). The locations of the bound peptides were determined from a F o -F c difference electron density maps. Models were rebuilt using COOT 42 , and refinement was done with phenix.refine of the PHENIX suite 43 . The overall assessment of model quality was performed using MolProbity 44 . The crystal parameters, data collection statistics, and final refinement statistics are shown in Table 3. All structural figures were generated with the PyMOL Molecular Graphics System, Version 1.7 (Schrödinger).
Sequence alignment. Sequence of PTPN3 (accession number NP_002820.3) was used as query on the InterEvolAlign server 45 to retrieve one single homolog per species assessed as probable ortholog through a reciprocal blast search procedure against the non-redundant database. Retrieved full-length sequences were re-aligned using MAFFT 46 and displayed using Jalview 47 .

Data Availability
All data generated or analysed during this study are included in this published article.