The GTPase-activating protein p120RasGAP has an evolutionarily conserved “ FLVR-unique ” SH2 domain

The Src homology 2 (SH2) domain has a highly conserved architecture that recognizes linear phosphotyrosine motifs and is present in a wide range of signaling pathways across different evolutionary taxa. A hallmark of SH2 domains is the arginine residue in the conserved FLVR motif that forms a direct salt bridge with bound phosphotyrosine. Here, we solve the X-ray crystal structures of the C-terminal SH2 domain of p120RasGAP ( RASA1 ) in its apo and peptide-bound form. We find that the arginine residue in the FLVR motif does not directly contact pTyr 1087 of a bound phosphopeptide derived from p190RhoGAP; rather, it makes an intramolecular salt bridge to an as-partic acid. Unexpectedly, coordination of phosphotyrosine is achieved by a modified binding pocket that appears early in evolution. Using isothermal titration calorimetry, we find that substitution of the FLVR arginine R377A does not cause a sig-nificant loss of phosphopeptide binding, but rather a tandem substitution of R398A (SH2 position b D4) and K400A (SH2 position b D6) is required to disrupt the binding. These results indicate a hitherto unrecognized diversity in SH2 domain interactions with phosphotyrosine and classify the C-terminal SH2 domain

shallow cleft-within the ;100-amino acid globular domain. Linear phosphotyrosine peptides bind perpendicular to the b-sheet in a two-pronged interaction with the pocket and cleft, a mode of binding that is reliably mirrored in cells and in the purified setting (4, 14). The deep pocket binds the pTyr residue, which is captured by electrostatic interactions with an arginine residue invariant in all pTyr-binding SH2 domains (9). In contrast, the shallow cleft binds residues C-terminal to the pTyr and varies considerably between SH2 domains allowing specificity determination (8,13,19,20). This two-pronged interaction also dictates a consistent orientation of the bound phosphopeptide N to C terminus with respect to the SH2 domain (18). In v-Src, the deep pocket arginine residue is part of the Phe 172 -Leu 173 -Val 174 -Arg 175 sequence, or "FLVR motif" (15), and arginine at this position (notated as the fifth residue on strand bB, bB5) is conserved in 117 of 120 human SH2 domains (9). Multiple lines of evidence indicate that the FLVR arginine is required for SH2-pTyr binding. To date, all structural studies of SH2 domain interactions with pTyr have demonstrated direct interactions between the FLVR arginine and pTyr. Further, the binding affinity of unphosphorylated peptides is on the order of 1000-fold weaker than phosphopeptides (15,18). Additionally, the FLVR arginine was found to be the primary contributor of binding free energy (21,22). Consequently, mutations of this residue are invariably used to generate a "dead" SH2 domain (23,24). p120RasGAP (RASA1, RasGAP, Ras GTPase-activating protein 1) was one of the first SH2 domain proteins to be identified (25)(26)(27) and was the first GTPase-activating protein (GAP) to be discovered (25,(28)(29)(30). It is ubiquitously expressed and required for life, because animals without p120RasGAP have major vascular defects (31,32). p120RasGAP contains two SH2 domains at its N terminus that sandwich an SH3 domain, followed by PH and C2 domains for membrane recruitment and a RasGAP domain (Fig. 1A) (30,33,34,84). The SH2 domains are used to directly interact with multiple phosphorylated binding partners including the p190RhoGAPs, the Eph receptor tyrosine kinases, and the Dok scaffolding proteins (32). These interactions are correlated with altered RasGAP activity and consequently with regulation of Ras signaling (35)(36)(37)(38)(39). The p120RasGAP SH2 domains therefore play critical roles in spatial-temporal regulation of Ras signaling by their interactions with this wide array of partners.
The SH2 domains of p120RasGAP are thought to be canonical SH2 domains that mediate direct interactions with pTyr This article contains supporting information. * For correspondence: Titus J. Boggon, titus.boggon@yale.edu. residues using their FLVR arginine residue, which is conserved in both domains. We recently confirmed this to be the case for the N-terminal SH2 domain (40); however, in contrast we now demonstrate that the C-terminal SH2 domain of p120RasGAP is a novel SH2 domain. Using X-ray crystallography, we find that the bB5 FLVR arginine does not contact phosphotyrosine pTyr 1087 of a bound p190RhoGAP peptide; instead, it makes a salt bridge to residue Asp 380 . Analysis of 715 aligned SH2 domain structures shows that this position of the FLVR arginine is rare, and point mutagenesis demonstrates that the FLVR Figure 1. Structure of p120RasGAP C-terminal SH2 domain. A, schematic of p120RasGAP interaction with p190RhoGAP. Domains are depicted, and the region co-crystallized is shown in a dashed box. B, structure of apo p120RasGAP C-SH2 indicating secondary structure elements and locations of the pTyr-binding pocket and specificity cleft. C, structure of p120RasGAP C-SH2 in complex with a synthesized phosphopeptide corresponding to p190RhoGAP-A residues 1086 DpYAEPMDA 1093 . Simulated annealing omit F obs 2 F calc difference map contoured at 3s RMSD is shown. D, surface electrostatics for p120RasGAP C-SH2 with p190RhoGAP-A peptide. E, interactions observed between p120RasGAP C-SH2 (green) and p190 phosphopeptide (yellow) defined by PDBsum (84). Hydrogen bonds are shown by red lines; nonbonded elements are shown by dashed lines. F, alignment of secondary structure features for p120RasGAP C-SH2, compared with p120RasGAP N-SH2 (PDB code 6PXC) (39), and Src (PDB code 1SPS) (18). b-Strands are highlighted yellow, and a-helices are highlighted orange. Residues that contact p190 phosphopeptide as defined by PDBsum are indicated with bold and underlined text. Residues discussed in the text are indicated.
arginine is not required for pTyr binding. Instead, pTyr binding is mediated by an alternate array of residues, including an unusual Arg 398 at the bD4 position. These findings demonstrate that the C-terminal SH2 domain of p120RasGAP is "FLVRunique." Results p120RasGAP interaction with p190RhoGAP is critical for recruitment of RhoGAP activity to sites of cell adhesion and for suppression of RasGAP activity at these locations (35,36,(41)(42)(43). Contacts between p120RasGAP and p190RhoGAP are mediated by the two SH2 domains of p120RasGAP (termed N-SH2 and C-SH2), which bind to phosphorylated tyrosine residues Tyr 1087 and Tyr 1105 of p190RhoGAP (44,45); both pTyr residues reside in the preferred pYXXP sequence recognized by both SH2 domains of p120RasGAP (13,19). We previously reported the crystal structure of N-SH2 of p120RasGAP and investigated its interaction with a p190RhoGAP pTyr 1105 phosphopeptide, which revealed a canonical SH2 domain structure and pTyr peptide-binding mode with K d of 0.3 6 0.1 mM (40). In the present study, we aim to determine the structure and pTyr-binding mode of C-SH2 of p120RasGAP. Toward this end, we expressed and purified the isolated C-SH2 domain recombinantly and performed crystallization studies. We obtained crystals of the apo form of p120RasGAP C-SH2 and solved the structure to 1.5 Å resolution. To examine the structural basis of pTyr binding, we also solved a 1.5 Å co-crystal structure of p120RasGAP C-SH2 with a pTyr 1087 p190RhoGAP phosphopeptide.
The structure of the apo form of C-SH2 ( Fig. 1B and Table 1) reveals a typical overall SH2 fold that is most similar to the p120RasGAP N-SH2 (PDB code 6PXC) (40) with root-meansquared deviation (RMSD) of ;1.3 Å over 94 Ca atoms and 31% sequence identity; it is also highly similar to the C-terminal SH2 domain of PLCg-1 (46) (PDB code 5TQ1; RMSD, ;1.8 Å over 101 Ca atoms, 27% identity) and Nck2 (47) (PDB code 2CIA; RMSD, 1.1 Å over 93 Ca atoms, 25%). The two-pronged pTyr pocket and specificity cleft interaction sites (16,18,48) are clearly visible in p120RasGAP C-SH2 (Fig. 1B), with a strongly electropositive deep pocket and a hydrophobic shallow cleft both available to interact with a linear peptide. We then determined the 1.5 Å co-crystal structure of C-SH2 in complex with a synthetic phosphopeptide corresponding to p190Rho-GAP residues 1086-1092 ( 1086 DpYAEPMD 1092 ) ( Fig. 1C and Table 1). The structure of C-SH2 in complex with phosphopeptide is experimentally similar to the apo form (RMSDs 0.9 Å over 105 Ca atoms and 1.0 Å over 102 Ca atoms for chains A and B, respectively). As expected, the N-to C-terminal orientation of the bound phosphopeptide is consistent with other SH2 domain structures (18) and is dictated by placing pTyr 1087 into the deep electrostatic pocket and Pro 1090 into the shallow cleft, recapitulating canonical electrostatic and van der Waals interactions (Fig. 1D). The residues of p120RasGAP C-SH2 that contact the phosphopeptide are generally similar to previously studied SH2-phosphopeptide interactions (16,18,48) (Fig. 1, E and F). Curiously, however, we observed that the FLVR motif arginine residue, Arg 377 , is oriented differently to other SH2 domains in both the apo and peptide-bound crystal forms. We thus investigated this major structural difference in detail.
In pTyr-binding SH2 domains, the conserved FLVR arginine at bB5 is required to form the base of the electropositive pocket and to hydrogen bond to pTyr (21,22). Unexpectedly, in the p120RasGAP C-SH2/phosphopeptide co-crystal structure, the FLVR arginine Arg 377 does not contact pTyr directly. Instead, Arg 377 makes a salt bridge to Asp 380 (at position BC1) ( Fig. 2A), an interaction that is also observed in the apo C-SH2 structure (Fig. 2B). Therefore, unlike typical SH2 domains, C-SH2 Arg 377 does not orient toward the phosphotyrosine-binding site in the absence of pTyr, nor does it undergo conformational change to contact pTyr directly in the presence of phosphopeptide. This unique orientation contrasts with p120RasGAP's N-SH2 domain, which binds phosphotyrosine in a canonical fashion (Fig.  2C) (40).
To assess whether the salt-bridge engagement of FLVR Arg 377 with Asp 380 in p120RasGAP C-SH2 is unique among determined SH2 domains structures, we conducted in silico analysis. We find that such an orientation is rare among the 715 aligned SH2 domains identified by the DALI server (49). At the time of this analysis, there are only two other examples of FLVR arginine residues that form interactions with another residues within the SH2 domain itself: 1) in the STAT6 SH2 domain, the FLVR arginine makes salt-bridge contacts to both pTyr and Asp at position BC1 (50); and 2) in the VAV SH2 domain when bound to an unphosphorylated tyrosine, the FLVR arginine hydrogen bonds to Gln at position BC1 (51). The atypical orientation of Arg 377 can be observed by superposition of aligned SH2 domains, in which the Arg 377 side chain is pointed away from the pTyr-binding site, unlike the positions of a majority of the typical arginine side chains (Fig. 2D). The FLVR Arg of p120RasGAP C-SH2 is therefore unique among structures of SH2 domains.
The molecular basis of this unique FLVR arginine orientation seems to be dictated by both the salt bridge to Asp 380 and by steric interference by Tyr 389 (residue bC5) (Fig. 2, B and C). Tyrosine at position bC5 is not observed in any other human SH2 domain and is usually a small amino acid: over the 120 human SH2 domains, residue bC5 is observed as Ser (63 of 120 times including N-SH2 of p120RasGAP), Thr (27 times), Ala (13 times), Cys (10 times), Gly (3 times), Val (2 times), Met (1 time), and Tyr (1 time, p120RasGAP C-SH2) (1). Small amino acids at bC5 allow the FLVR arginine to engage the pTyr directly as observed in p120RasGAP N-SH2 bound to a phosphopeptide ( Fig. 2C). At position BC1 (equivalent to Asp 380 in p120RasGAP C-SH2), an acidic residue is frequently observed (Asp, 6 times and Glu, 38 times), but in many SH2 domains it caps helix aB (e.g. Glu 179 in Fyn SH2; Fig. 2E). In contrast, in p120RasGAP C-SH2 a helix capping interaction by BC1 is not possible because the FLVR arginine guanidino group prevents close arrangement of helix aB and strand bB. The position of the FLVR arginine therefore seems to accommodate atypical orientations of other elements of the p120RasGAP C-SH2 domain.
Upon inspection of the p120RasGAP C-SH2 structure in complex with phosphopeptide, we observe several additional unique features of pTyr binding in addition to the orientation of the FLVR arginine and presence of bC5 tyrosine. Across SH2 domains, three major interactions have been observed between the pTyr and its binding pocket: 1) the salt bridge between the pTyr and the FLVR motif bB5 arginine (Arg 207 in N-SH2), 2) binding to a basic residue at either position aA2 (Arg 188 in N-SH2) or bD6, and 3) binding to residues of the BC loop (between the bB and bC strands (Ser 209 in N-SH2; Figs. 1F and 3A) (21,40,52). Consistent with these interactions, p120Ras-GAP C-SH2 uses bD6 (Lys 400 ) and residues in the BC loop (Ser 379 , Asn 381 , and Thr 382 ; Fig. 3B). However, in contrast, p120RasGAP C-SH2 uses additional residues bC3 (Ser 387 ) and a basic residue at position bD4 (Arg 398 ) to bind pTyr (Figs. 1, E and F, and 3B). Arg 398 at position bD4 is unique to p120Ras-GAP C-SH2; this residue is most commonly a histidine (82 of 120 human SH2 domains; His 229 in N-SH2; Fig. 3A) (1). The unusual binding site also manifests in the location of the phosphate-when phosphate atoms are mapped, C-SH2 binds to pTyr in a location divergent to all previously determined SH2 domains (Fig. 3C). The p120RasGAP C-SH2 pTyr-binding pocket therefore diverges from either the Src-like (where pTyr is coordinated by an Arg at position aA2) or SAP-like (where pTyr is coordinated by a basic residue at position bD6) pockets (52). Sequence alignment of human SH2 domains suggests that no other SH2 domain harbors dual basic residues at positions bD4 and bD6 (1), potentially indicating an evolution of the site to compensate for the loss of direct FLVR arginine binding. Additionally, the amino-aromatic interaction typically contributed by the arginine at aA2 (15,16) is instead fulfilled by the unique Arg 398 at bD4 in C-SH2 (Fig. S1).
Many SH2-pTyr interactions have been studied in solution, and the measured binding affinities range in the 10 25 to 10 28 M (10 mM to 10 nM), or 27 to 211 kcal/mol range (53). We therefore used isothermal titration calorimetry (ITC) to measure the affinity of p120RasGAP C-SH2 with pTyr 1087 phosphopeptide from p190RhoGAP and find the resultant K d = 0.15 6 0.04 mM, approximately 29 kcal/mol, to be within this expected range ( Table 2 and Fig. S2). We next used ITC to assess the extent of binding of pTyr 1087 phosphopeptide to C-SH2 mutants. For canonical SH2-pTyr interactions, the FLVR arginine is the primary contributor of binding free energy (21,22), and mutation of this residue abrogates binding (23,24). However, the unusual nature of the p120RasGAP C-SH2 suggests that the basis for its interaction with pTyr diverges from canonical SH2-pTyr inter-actions. We therefore tested whether Arg 377 contributes to pTyr binding. Using ITC, we find that R377A mutation leads to slight reduction in affinity from WT K d = 0.15 6 0.04 mM to    Table S1).  (Table 2 and Fig. S2). To our knowledge, this is the first SH2 domain studied to date that does not suffer a major loss of pTyr binding when the FLVR arginine residue is mutated. To further define the residues critical for pTyr binding, we introduced alanine point mutations at other basic residues that directly bind the pTyr: Arg 398 at bD4 and Lys 400 at bD6. Using ITC, we find that although the single mutants R398A and K400A only modestly impact pTyr peptide binding (K d values of 0.31 6 0.20 and 0.81 6 0.15 mM, respectively), in combination, the double R398A/K400A mutant results in an ;40-fold loss of binding (K d of 6.24 6 4.2 mM; Table 2 and Fig. S2). This indicates that unique among SH2 domains, the p120RasGAP C-SH2 requires multiple point mutations to abrogate pTyr binding.
To assess the evolution of the p120RasGAP C-SH2 domain, we generated an alignment of 209 p120RasGAP sequences. We find that p120RasGAP is present in mammals, invertebrates, sponges, the choanoflagellates Monosiga brevicollis and Salpingoeca rosetta, the placozoa Trichoplax sp. H2, the orthonectid Intoshia linei, and in the single-celled eukaryote Capsapora owczarzaki (Figs. 1A and 3D and Fig. S3); notably, the domain architecture is preserved throughout phylogeny. We next examined the conservation of the unique phosphotyrosinebinding site. We observe that many of the phosphate-binding residues are well-conserved. However, we observe that a bulky residue at bC5 (Tyr 389 in human), which sterically hinders canonical orientation of the FLVR arginine, which is retained in vertebrates and many invertebrates as Tyr or Phe, is a small residue (mostly Ser) in corals and more ancient species (Fig. S3). Similarly, the unique Arg 398 at position bD4 is highly conserved in vertebrates and invertebrates but is a His in choanoflagellates and in C. owczarzaki. The evolutionary alterations in the unique pTyr-binding site therefore seem to indicate that p120RasGAP's C-terminal SH2 domain originally had a canonical binding site but that it evolved to its FLVR-unique conformation.

Discussion
Among protein domains the SH2 family is extraordinarily well-studied, making it unexpected for major divergence to have gone unidentified and even less expected that major divergence should be identified in one of the founding members. Nonetheless, we have shown that the C-terminal SH2 domain of p120RasGAP, the prototypical RasGAP and one of the earliest identified SH2 domains, is divergent from all studied SH2 domains. The lack of FLVR motif arginine contact with phosphotyrosine is unique among SH2 domains; in fact, even SH2 domains that can bind unphosphorylated partners do so in a FLVR arginine-dependent manner (e.g. SAP can bind Tyr as well as pTyr peptides) (8,54). We therefore term the p120RasGAP C-SH2 a FLVR-unique SH2 domain.
These studies, using the isolated C-SH2 domain and single pTyr peptide, do not rule out the possibility that in the context of full-length proteins, potential domain-domain interactions within the p120RasGAP SH2-SH3-SH2 cassette (Fig. 1A) might alter the pTyr-binding site of C-SH2 to a more conventional FLVR-driven conformation. Alternatively, interdomain contacts might create an alternative unique mode of pTyr binding, similar to the tyrosine kinase ZAP70, which contains two SH2 domains separated by a short helical linker domain and binds two pTyr targets in the T-cell receptor. Specifically, the two ZAP70 SH2 domains come together to create an interface that forms one unique pTyr-binding site, whereas the other more typical pTyr-binding site is contained within a single SH2 domain (55). Future studies utilizing longer p120RasGAP constructs and dual pTyr-binding partners will help to examine these possibilities.

Classification of p120RasGAP C-SH2
Canonically, the FLVR arginine is required for interactions with pTyr peptides, contributing over 50% of their free energy of binding to the interaction (22,56), and mutations of this residue result in an effectively "dead" SH2 domain. This residue is highly conserved, and there are only three human SH2 domains that do not contain the FLVR arginine residue (RIN has a His at this position, SH2D5 has a Trp, and Tyk2 has a Met) (9). For Tyk2, this belies the Janus kinase FERM-SH2 module mediating direct interaction with nonphosphorylated cytoplasmic tails of cytokine receptors (57,58). The lack of diversity at the FLVR arginine position indicates conserved function, which was recently confirmed in bacteria in which a large number of SH2 domains were identified (52). Bacterial SH2 domains are classified in two groups, both of which are structurally divergent from eukaryotic SH2 domains, but even these divergent bacterial SH2 domains bind pTyr using the conserved FLVRarginine (52). The C-terminal SH2 of p120RasGAP therefore seems to have evolved uniquely among the SH2 family of proteins.
The two-pronged pocket and cleft interaction site found in most SH2 domains (16,18,48) can be classified into different groups (groups IA to IE, IIA to IID, and III) that have divergent specificities, with the majority displaying a binding preference for the residue at the 12, 13, or 14 position C-terminal to the pTyr (13, 19) (although P 1 1, P . 4, and regions N-terminal to the pTyr can also influence specificity (59)(60)(61)(62)). The determinants of the specificity cleft are controlled primarily by two loops: one between the E and F b-strands (the EF loop) and one between a-helix B and the b-strand G (the BG loop). These can be thought of as analogous to the complementarity-determining regions, specificity-determining loops of antibodies (13,19,20). In this classification scheme, the p120RasGAP Cterminal SH2 domain is classified as a group IB SH2 domain, with specificity for hydrophobic residue at position 13 (13,19). Our crystal structures confirm the interaction site with these loops (Fig. 1).

Specificity of C-SH2 for phosphotyrosine
Two determinants of SH2 domain-binding specificity for phosphotyrosine over phosphoserine or phosphothreonine are 1) the depth of the binding pocket and 2) presence of aminoaromatic interactions (15,16,(63)(64)(65). For p120RasGAP C-SH2 bound to a pTyr-containing peptide, we observe the typical deep, elongated pocket to accommodate the pTyr residue; the groove is lined by Arg 398 and Lys 400 , which cradle the aromatic ring. This amino-aromatic interaction between Arg 398 and the pTyr ring is similar to other typical SH2 domains such as Src and Lck (15,16); however, Arg at the bD4 position rather than aA2 is unique to C-SH2. Taken together, these observations suggest that p120RasGAP has binding specificity for pTyr residues.

NMR solution structure of C-SH2
The NMR solution structure of p120RasGAP C-terminal SH2 domain, residues 340-446, was determined by the RIKEN Structural Genomics/Proteomics Initiative in 2006 and deposited in the Protein Data Bank (code 2GSB). The solution structure contains the 20 lowest energy models. Overall, the superposition with our crystal structures is close (RMSD 1.12 Å over 101 Ca atoms) (Fig. S4A), but in-solution conformational flexibility is observed in the EF loop, which defines 13 specificity (19), and in the BC loop, which harbors Asp 380 . None of the NMR structures exhibit the bidentate salt bridge between Arg 377 and Asp 380 (residue BC1), and both residues display extensive conformational variability, but their overall orientation is similar to our crystal structures (Fig. S4B). In contrast, Tyr 389 is in a broadly similar position to our crystal structures and blocks orientation of the FLVR Arg toward the canonical pTyr-binding position. The unpublished NMR structure therefore supports our crystallographic data that p120RasGAP C-SH2 is a FLVR-unique SH2 domain.

Functional role of the FLVR-unique C-SH2
What then might the function of this highly unusual SH2 domain in p120RasGAP be? SH2 domains seem to have helped facilitate the evolutionary increase in complexity of signal transduction pathways and the transition from unicellular to multicellular organisms (as illustrated by a single SH2 domain residing in baker's yeast, Saccharomyces cerevisiae) (10). In humans there are ;120 proteins that contain SH2 domains, but only 10 of these have dual SH2s. For p120RasGAP, the bivalent SH2 domains probably indicate that p120RasGAP has fast rebinding and long dwell times at pTyr-binding partners (66), and cooperation between the p120RasGAP domains is thought to impact signal transduction (7) with conformational changes proposed to occur on dual engagement of the SH2 domains with phosphotyrosine partners (44). However, the affinities of SH2 domain interactions with their functional phospho-partners is generally in the moderate 0.1-10 mM range (56, 67), allowing ready dissociation and thus preventing masking of the pTyr site and prevention of signal transduction (68,69). For p120RasGAP, the combination of two tight SH2-pTyr interactions may result in extremely long dwell times that are deleterious for signal transduction. It may be that the altered pTyrbinding site in the C-terminal SH2 domain beneficially impacts p120RasGAP's signaling by tuning recruitment and retention at pTyr partners and thus prevents masking (68, 69) of these sites.

Broader implications
Disruption of SH2-pTyr interactions has theoretical clinical potential to regulate diverse signal transduction pathways, and consequently much work was conducted to achieve SH2 domain-specific inhibitors. Clinically useful selectivity has not, however, been achieved in large part because of bioavailability and the molecular similarities between SH2 domains (21). Selective picomolar binders can be designed where SH2 domains diverge as demonstrated for Grb2, which has an unusual specificity pocket that recognizes Asn at residue pY 1 2 (70)(71)(72). Although it remains an outside possibility, nonetheless, it is interesting to speculate that the unique nature of p120RasGAP's C-terminal SH2 domain may represent a novel SH2-inhibitor target with the potential to beneficially alter both Ras and Rho signaling.
SH2 domains have played an important role in influencing our understanding of how cytosolic signaling occurs. Invariably these domains bind phosphotyrosine partners with their FLVR motif arginine residue acting as the linchpin of the interaction. It is striking, therefore, that one of the first identified SH2 domain proteins should diverge from this paradigm. The functional reasons for this divergence are currently unclear, but the array of bidentate binding partners for p120RasGAP and alterations in p120RasGAP's RasGAP activity on binding to phosphorylated partner proteins may hint at an evolutionary requirement to allow unmasking of the phosphotyrosine sites. The discovery of the unique nature of the C-terminal SH2 domain and how to alter its phosphotyrosine binding may therefore provide guidance to resolving how p120RasGAP functions mechanistically.

Materials and methods
Expression and purification p120RasGAP C-SH2 domain cDNA encoding the C-terminal SH2 domain of human p120RasGAP (UniProt ID P20936; residues 340-444) was amplified by PCR and ligated into a modified pET vector, which includes an N-terminal His 6 tag and TEV protease recognition site. Two native cysteine residues, Cys 372 and Cys 402 , were mutated to serine by QuikChange mutagenesis (Agilent) to prevent formation of intermolecular disulfide bonds. The following point mutants were also generated by QuikChange mutagenesis: K377A, K398A, K400A, and K398A/K400A. Protein expression of WT and mutant C-SH2 was performed in Rosetta (DE3) cells, which were cultured in 1 liter of Luria broth at 37°C to an A 600 of 0.6-0.8 and then cooled to 18°C, and protein expression was induced with 0.2 mM isopropyl b-D-thiogalactopyranoside. The cells were harvested by centrifugation, resuspended in lysis buffer (50 mM HEPES, pH 7.3, and 500 mM NaCl), and lysed by freeze-thaw cycles in the presence of lysozyme followed by sonication. Total cellular lysate was clarified by centrifugation at 5000 3 g at 4°C and applied to nickelnitrilotriacetic acid-agarose resin (Qiagen) for 1 h at 4°C to capture His 6 -tagged protein. Beads with bound protein were washed with 20 column volumes of wash buffer containing 50 mM HEPES, pH 7.3, 500 mM NaCl, 20 mM imidazole. The His 6 tag was proteolytically removed from the C-SH2 proteins "on bead" overnight at 4°C by the addition of TEV protease, which itself is also His 6 -tagged and captured by the nickel-nitrilotriacetic acid resin. The flow-through containing untagged C-SH2 protein was collected and applied to size-exclusion chromatography (Superdex 75; GE Healthcare) in buffer containing 20 mM Tris, pH 7.4, 150 mM NaCl. Finally, C-SH2 proteins were concentrated in a centrifugal filter with a molecular mass cutoff of 3,000 Da (Amicon Ultra, Millipore Sigma). 1 liter of Rosetta (DE3) cell culture resulted in a final purified protein yield of ;20 mg for WT and up to 10 mg for mutant.
Crystallization, data collection, structure determination, and refinement p120RasGAP C-SH2 WT protein was used in crystallization trials at ;14 mg/ml. Initial crystal screening was conducted with Index HT kit (Hampton Research) by a TTP Labtech Mosquito in sitting-drop vapor-diffusion trays at room temperature. Single crystals were obtained in Index HT position A3 containing 2.0 M ammonium sulfate, 0.1 M Bis-Tris, pH 6.5, with a 1:1 (v:v) protein:reservoir solution ratio. Optimization of this crystallization condition was achieved in hanging-drop vapor-diffusion plates, with a reservoir buffer containing 2.3 m ammonium sulfate, 0.1 M Bis-Tris, pH 6.5, and ratio of 1:1 (v:v) protein:reservoir solution. Single crystals with approximate dimensions 200 3 200 3 200 mm were harvested from the drop, cryopreserved in reservoir solution supplemented with 20% ethylene glycol, and flash-cooled in liquid nitrogen. X-ray data collection on a single crystal was performed at Northeastern Collaborative Access Team Beamline 24-ID-C at Argonne National Laboratory Advanced Photon Source. X-ray data were processed and scaled in HKL2000 (73) in space group P2 1 2 1 2 1 with the unit cell dimensions a = 52.5 Å, b = 65.6 Å, c = 71.6 Å, a = b = g = 90°, to 1.50 Å resolution. Matthews probability predicted two copies of SH2 in the asymmetric unit, and a molecular replacement solution confirmed the prediction with copies of C-SH2 obtained by Phenix Phaser (74) using the SH2 domain of SAP (PDB code 1D4T) (54) as a search model, yielding the translational function Z score of 12.7. Model building was performed in Phenix Autobuild (75), which successfully built 196 residues and correctly placed 192 in sequence (residues 344-442 of copy A and 350-442 of copy B). Manual model building was performed in Coot (76) and refinement in Phenix (77). Two sulfate ions (from the crystallization drop) and six ethylene glycol molecules (from the cryopreservative solution) were also modeled into density. Final refinement statistics are R work = 17.9% and R free = 19.7%.
For co-crystallization with the 7-amino acid p190RhoGAP pTyr 1087 phosphopeptide, C-SH2 protein at 800 mM (10 mg/ml) was premixed with phosphopeptide concentrations ranging from 4 to 8 mM. Initial crystallization screens were performed with Index HT and SaltRx HT screens (Hampton Research) on a TTP Labtech Mosquito into sitting drops. Optimized co-crystals were obtained with reservoir solution containing 1.2 M sodium citrate tribasic dihydrate, 0.1 M Tris, pH 8.5. Single crystals were cryopreserved in reservoir buffer supplemented with 0.5 M sodium malonate, pH 7.0, before being flash-cooled in liquid nitrogen. X-ray data collection on a single crystal was performed at Northeastern Collaborative Access Team Beamline 24-ID-C at Argonne National Laboratory Advanced Photon Source. X-ray data were processed in HKL2000 (73) in space group C222 1 with unit cell dimensions a = 63.1 Å, b = 83.9 Å, c = 54.2 Å, a = b = g = 90°to 1.50 Å resolution and one copy per asymmetric unit. For structure solution, an all-alanine model derived from the NMR structure of p120RasGAP C-SH2 (PDB code 2GSB), truncated to residues 345-442 and B factors set to 20, was used as a search model for molecular replacement. Molecular replacement was performed by Phaser (74), which found a single solution for one copy of C-SH2 with a TFZ score of 10.6. Autobuilding was performed in Phenix (75), which removed model bias and successfully built and placed 100 residues (residues 342-442). Autobuilding also resulted in the building of five residues of the phosphopeptide, corresponding to p190RhoGAP residues 1087-1091. Manual model building was performed in Coot (76) and refinement in Phenix (77), yielding final R work = 16.5% and R free = 19.0%.

Isothermal titration calorimetry
Both C-SH2 WT and mutant proteins and pTyr 1087 phosphopeptide (15 amino acids) were prepared for ITC by overnight dialysis in a common buffer with a 20 mM Tris, pH 7.4, 150 mM NaCl composition. Slide-A-Lyzer dialysis cassettes were used with a molecular mass cutoff of 3,500 Da were used for protein dialysis, and Micro Float-A-Lyzer dialysis devices with a 100-500-Da cutoff were used for peptide dialysis. The samples were retrieved from their cartridges and spun down for 10 min at 4°C. The concentrations were measured by Nanodrop (Thermo Fisher). To determine peptide concentration, a phosphotyrosine extinction coefficient of 458.6 M 21 cm 21 at pH 7.4 was used (78). For ITC, a Nano-ITC (TA Instruments) was used. 350 ml of protein were injected into the sample cell. Both protein and peptide were degassed for 3 min prior to loading. The sample cell contents were stirred at 350 rpm at 25°C to achieve continuous mixing. The results were analyzed using Nano-ITC Analyze software.