|Home | About | Journals | Submit | Contact Us | Français|
Studies of cellular and tissue dynamics benefit greatly from tools that can control protein activity with specificity and precise timing in living systems. We describe here a new approach to confer allosteric regulation specifically on the catalytic activity of kinases. A highly conserved portion of the kinase catalytic domain is modified with a small protein insert that inactivates catalytic activity, but does not affect other protein interactions. Catalytic activity is restored by addition of rapamycin or non-immunosuppresive analogs (Fig. 1A). We demonstrate the approach by specifically activating focal adhesion kinase (FAK) within minutes in living cells, thereby demonstrating a novel role for FAK in regulation of membrane dynamics. Molecular modeling and mutagenesis indicate that the protein insert reduces activity by increasing the flexibility of the catalytic domain. Drug binding restores activity by increasing rigidity. Successful regulation of Src and p38 suggest that modification of this highly conserved site will be applicable to other kinases.
Recent novel methods for regulation of kinases with precise timing in living cells include induced dimerization, subcellular localization, proteolytic degradation or chemical rescue from an inactivating mutation1–4. Engineered allosteric regulation as well shows great promise for precise control of protein activity 5–7. Nonetheless, important challenges remain in that existing methods are limited to specific targets, inactivate rather than activate kinases, and/or do not enable regulation of a particular domain within the target. We describe here a new method to activate specifically the catalytic domain within a multidomain protein kinase, using FAK as a model. FAK has been implicated in a wide variety of cell behaviors, including proliferation, apoptosis, migration and tumorigenesis8–11. It is a multidomain protein that functions as both a scaffold and a kinase11 and relatively little is known about the specific role of its catalytic activity. It therefore served as a good test of the new method, which enabled us to specifically dissect the function of FAK kinase activity without affecting scaffolding functions, controlling it with a temporal resolution of 1–2 minutes.
To allosterically regulate FAK’s catalytic activity we used a portion of the small protein FKBP12; a previous study showed that ligand binding to FKBP12 greatly increased its conformational rigidity 12, suggesting that insertion of FKBP12 near the catalytic site of kinases could be used to control the conformational mobility of the kinase active site. It was, however, unclear that FKBP12 could be inserted into the middle of the kinase sequence without severely disrupting kinase structure or FKBP12 binding interactions. We therefore experimented with truncated forms of FKBP12, leading to an FKBP12 derivative named iFKBP (insertable FKBP, Fig. 1B). In iFKBP, the N and C termini are positioned near one another for minimal perturbation of kinase secondary structure (Fig 1B). Co-immunoprecipitation experiments showed that iFKBP interacts with rapamycin and FKBP12-Rapamycin Binding domain (FRB) as efficiently as does wild type FKBP12, even when inserted in the middle of the FAK molecule (Fig. 1C, Supplementary Fig. S1). Molecular dynamics studies of iFKBP indicated that its conformational fluctuation is reduced by interaction with rapamycin or by rapamycin-induced heterodimerization with FRB (Fig. 1D and Supplementary Fig. S2). Changes in conformational fluctuations were especially pronounced at the N and C termini where iFKBP would be linked to FAK, suggesting that the effects of rapamycin/FRB binding could be communicated to FAK.
Optimization of the insertion site and the linkers connecting iFKBP to FAK led to a version of FAK that was susceptible to regulation by rapamycin-induced FRB binding. With insertion of iFKBP at Glu445 (FAK-iFKBP445 construct), FAK catalytic activity was dramatically reduced. Rapamycin-induced binding to FRB restored activity (Fig. 2A). Treatment with rapamycin/FRB did not affect the activity of wild-type FAK (FAKwt) or a construct with iFKBP attached to the FAK N-terminus, demonstrating that regulation of catalytic activity is dependent on specific placement of the insert in the catalytic subunit. To optimize regulation of FAK by rapamycin, several modifications were introduced into the regions where iFKBP was connected to FAK. iFKBP was positioned within the FAK loop Met442-Ala448, between two β-strands in the N-terminal lobe of the FAK catalytic domain (Fig. 2B). Replacing FAK residues Met442-Ala448 with iFKBP, using no linkers, negated the effect of iFKBP on FAK activity and dramatically reduced interaction with rapamycin and FRB (Figs. 2A and 2B, construct FAK-iFKBP 442–448). Computational analysis revealed that the construct without linkers is locked in a distorted conformation that prevents ligand binding (Supplementary Fig. S3). In contrast, introduction of short linkers to connect iFKBP with the β-strands of the FAK catalytic domain led to the optimized structure used henceforth (named RapR-FAK, for Rapamycin-regulated FAK). In RapR-FAK, activity in the absence of rapamycin was significantly lower than that of FAK-iFKBP445 (Fig. 2A). Rapmycin-induced FRB binding restored activity to near wild type level. Activation of RapR-FAK catalytic activity was achieved in living cells within 2 minutes and with 50 nM rapamycin(Fig. 2C and D). Activation was also achieved by treatment with rapamycin alone, without co-expression of FRB (Supplementary Fig. S4). However, this required significantly higher concentrations of rapamycin (up to 4 μM), so the remaining studies described here were carried out using rapamycin-induced FRB binding. Computational analysis indicated that rapamycin alone does not stabilize iFKBP to the same extent as rapmycin/FRB (Fig. 1D and Supplementary Fig. S2).
iFKBP-mediated FAK regulation was designed to specifically control catalytic activity without perturbing other FAK functions. Thus, it was important to test the effects of iFKBP insertion on normal FAK binding interactions and FAK regulation. FAK catalytic activity is regulated by an autoinhibitory interaction between the N-terminal FERM domain and the catalytic domain 13. Two amino acids known to be involved in this interaction were mutated to alanines (Y180A and M183A, previously described 13) to test if RapR-FAK remains regulated by autoinhibition. When activated by rapamycin, the Y180A/M183A construct (RapR-FAK-YM) demonstrates significantly higher activity than RapR-FAK (Fig. 2E), consistent with published results for constitutively active FAK 13 and demonstrating that RapR-FAK is still regulated by autoinhibition. Importantly, RapR-FAK-YM is regulated solely by rapamycin, and not by endogenous mechanisms. To confirm that RapR-FAK phosphorylates substrates in a rapamycin-dependent manner in cells, phosphorylation of two known FAK substrates was tested before and after addition of rapamycin. Upon activation of RapR-FAK-YM, phosphorylation of paxillin on residue Tyr31 and autophosphorylation of FAK on residue Tyr397 are significantly increased (Fig. 2F). A control construct lacking catalytic activity (RapR-FAK-YM-KD, with additional mutation D546R) failed to demonstrate any change in phosphorylation. RapR-FAK and wtFAK showed similar binding to paxillin and Src in co-immunoprecipitation assays (Supplementary Fig. S5), indicating that introduction of iFKBP into the catalytic domain of FAK does not affect interaction with binding partners. Also, iFKBP insertion did not perturb the intracellular distribution of RapR-FAK; its localization was identical to that of wild-type FAK (Supplementary Fig. S6). Activation of RapR-FAK was accompanied by translocation of fluorescently labeled FRB into focal adhesions and co-localization with fluorescent RapR-FAK (Supplementary Fig. S7). The translocation of fluorescent FRB into adhesions served as a useful marker of FAK activation in live cells. Overall we conclude that RapR-FAK enables robust and specific activation of FAK catalytic activity in living cells without perturbation of other FAK properties.
FAK is known to be overexpressed and activated in human tumors 14–16, but the specific role of its catalytic activity remains unclear. To identify processes affected specifically by FAK catalytic activity, we examined the activation of RapR-FAK-YM in HeLa cells. The Y180A/M183A mutant was used to ensure the regulation of RapR-FAK by rapamycin only, and exclude modulation by endogenous upstream factors. Consistent with previous reports showing that catalytic activity is not required for FAK’s role in growth factor-stimulated motility17, activation of RapR-FAK-YM did not significantly affect cell movement (Supplementary Fig 8). However, we did observe a distinct effect on membrane dynamics. HeLa cells normally show small peripheral ruffles that remain near the cell border. Upon addition of rapamycin, the extent of ruffling greatly increased, and very large and dynamic ruffles appeared across the dorsal surface (Fig. 3A, B, Supplementary movie S1, 36/64 analyzed cells). In control studies, cells expressing similar levels of catalytically inactive RapR-FAK-YM-KD showed no change in normal ruffling activity (Fig. 3B, 34/35 analyzed cells). RapR-FAK was localized within these ruffles (Supplementary Fig. S9). Importantly, wild-type FAK was also detected in ruffles stimulated by RapR-FAK and in those produced by PDGF treatment (Supplementary Fig. S10, S11, S12), indicating that dorsal ruffles are not an artifact of RapR-FAK mislocalization. Furthermore, FAK-null fibroblasts failed to produce PDGF-stimulated dorsal ruffles (158 cells analyzed), whereas 50% of control fibroblasts expressing FAK (59 out of 118 analyzed) exhibited distinct dorsal ruffling under the same stimulation conditions. These data implicate FAK catalytic activity in the regulation of dorsal membrane protrusions.
Published work has demonstrated that FAK autophosphorylation of Tyr397 plays an important role in FAK-mediated signaling, and that Tyr397 phosphorylation level correlates with FAK activation18. Because autophosphorylation of FAK on Tyr397 creates a binding site for Src family kinases 18, 19 it has been proposed that interaction of FAK with Src leads to Src activation 18. Furthermore, Src is involved in the formation of dorsal protrusions stimulated by platelet derived growth factor (PDGF) 20. Together these observations led us to hypothesize that the FAK-stimulated formation of dorsal protrusions occurs via activation of Src. In our studies, mutation of Tyr397 to phenylalanine in RapR-FAK completely abolished the formation of dorsal protrusions (Fig. 3B). To test the potential role of Src, cells were treated with PP2, an inhibitor of Src family kinases, after stimulation of RapR-FAK-YM. This abrogated the FAK-induced dorsal ruffling (Fig 3C, Supplementary movie S2). In contrast, control compound PP3, an inactive PP2 stereoisomer, or imatinib, an inhibitor of Abl kinase, had no effect (data not shown). Phosphorylation of Src Tyr418 (Tyr416 in avian Src) is known to occur upon Src activation 21, 22. Rapamycin addition to cells transfected with RapR-FAK-YM led to increased Src Tyr418 phosphorylation, while cells expressing RapR-FAK-YM with an additional mutation that abolishes Src binding (Y397F mutation) showed no effect (Fig. 3D). Together, these data directly demonstrate that FAK catalytic activity stimulates Src, and that this in turn leads to dorsal protrusions. Dorsal protrusions play an important role in the invasive migration of cells into extracellular matrix 23 and enhanced FAK expression in tumor cells is associated with cell invasiveness. Our data suggests a mechanism whereby FAK overexpression contributes to cancer.
In order to understand the molecular mechanism of RapR-FAK allosteric regulation and explore the generalizability of the approach, we performed molecular dynamics simulations24, 25. Combined with the biochemical data, the computational analysis indicated a mechanism for iFKBP-mediated regulation. The point where iFKBP is inserted connects via a β strand to FAK’s Gly loop (G-loop), a structural feature critical for positioning the ATP phosphate groups in the catalytic site (Fig 4A) 26. Molecular dynamics analysis indicated that the conformational mobility of the G-loop is correlated with that of the FAK region where iFKBP is inserted (the ‘insertion loop’, Fig. 4B), suggesting that the dynamics of the insertion loop could affect the dynamics of the G-loop and thereby change the catalytic activity. Comparison of wt FAK and RapR-FAK dynamics indicated that the amplitude of G-loop conformational dynamics is dramatically increased when iFKBP is inserted in the catalytic domain. These dynamics decreased back to wild-type levels upon binding to rapamycin/FRB (Fig. 4C, D, supplementary movie S3). Based on this analysis, we postulate that the effectiveness of the G-loop in the phosphate transfer reaction is reduced due to greater conformational flexibility produced by insertion of iFKBP. Interaction with rapamycin and FRB stabilizes the G loop to rescue FAK catalytic activity. Molecular dynamics analysis was consistent with empirical measurements; dynamics analysis of the FAK-iFKBP445 variant suggested that its longer linkers decreased coupling between the iFKBP insert and G-loop dynamics (Supplementary Fig. S13), resulting in the less effective FAK inhibition observed in biochemical studies (Fig. 2A, FAK-iFKBP445 construct). In contrast, insertion of iFKBP without any linkers restricted the structural dynamics of iFKBP, consistent with the observed minimal effects on catalytic activity (Supplementary Fig. S13, FAK-iFKBP442-8 construct). In summary, computational analysis indicates that the allosteric modulation of RapR-FAK activity results from dynamic coupling of the optimized iFKBP insertion and the kinase G-loop, highly conserved structural features in all known kinases 26.
Because the mechanism of allosteric regulation is based on coupling of highly conserved structural elements, the RapR approach may well be applicable to other kinases. We explored this by inserting iFKBP into a tyrosine kinase, Src, and into a serine/threonine kinase, p38, at a site analogous to that used in FAK (Gly288 in Src, Lys45 in p38α) (Supplementary Fig. S14). In both Src and p38, insertion of iFKBP strongly inhibited activity, and activity was rescued by interaction with rapamycin/FRB (Fig. 4E, Supplementary Fig. S15). Treatment with rapamycin did not affect wild-type Src or control Src constructs in which iFKBP was added to the C-terminus, nor did it have any significant effect on wild-type p38. In molecular dynamics simulations, Src showed the same coupling between iFKBP and the Gly-loop that was observed for FAK (Supplementary Fig. S16, S17). These data suggest that the iFKBP cassette can be used for allosteric regulation of a wide variety of both tyrosine and serine/threonine kinases.
Although we saw no effects of rapamycin in the absence of RapR kinases, we were concerned that some potential studies could be complicated by the known immunosuppressive effects of rapamycin. We therefore tested the ability to regulate RapR kinases using known non-immunosuppresive analogs of Rapamycin, iRap and AP21967. Both compounds regulated RapR-FAK activity at concentrations comparable to those reported previously for dimerization of proteins in living cells 27 (Supplementary Fig. S18). Importantly, AP21967 and a similar analog of rapamycin (C20-MaRap) have been successfully used for experiments in animals 28, 29, indicating that the RapR method can be applied in live animal studies. The F36V mutant of FKBP, which interacts tightly with the Shield 1 compound 4, could potentially eliminate the requirement for FRB and minimize effects on endogenous FKBP12 function.
In summary, we describe a protein modification to confer rapamycin sensitivity specifically on the catalytic activity of kinases. The approach is based upon highly conserved regions in both serine/threonine and tyrosine kinases, promising broad applicability. It requires only addition of a small protein insert into the conserved portion of the catalytic subunit, and can be used with non-immunosuppresive rapamycin analogs suitable for in vivo studies. The approach combines the temporal resolution of small molecule inhibitors with the absolute specificity of genetic approaches, and enables allosteric regulation of a single domain in a multidomain protein. A mechanistic model based on molecular dynamics, and application to analogous sites in FAK, Src and p38α, indicate that rapamycin exerts its effect by modulating the conformational flexibility of the conserved catalytic subunit. By selectively activating FAK catalytic activity in living cells, we directly demonstrated that FAK catalysis activates Src to trigger large dorsal protrusions, a potential mechanism explaining how overexpression and activation of FAK contributes to tumor progression.
Methods and any associated references are available in the online version of the paper at http://www.nature.com/naturebiotechnology/.
We thank Jonathan Edwards, Daniel Dominguez and Vishal Rao for help with construction and testing of RapR-Src and RapR-p38α constructs, Betsy Clarke for her design of figures, and are grateful to the UNC Cancer Research Fund and the National Institutes of Health for funding (GM64346 and GM057464 to KMH; GM080742 and GM080742-03S1 to N.V.D).
Author Contributions A.V.K initiated the project, developed and validated regulation of RapR-kinases, and performed the studies of FAK biological function. F.D. performed molecular modeling of FKBP12 variants, RapR-FAK and RapR-Src. P.K. performed biochemical characterization of RapR-p38. N.V.D. coordinated molecular dynamics studies. K.M.H. coordinated the study and wrote the final version of the manuscript, based on contributions from all authors.
Author Information Reprints and permissions information is available at http://npg.nature.com/reprintsandpermissions/.