|Active site profiling reveals coupling between domains in SRC-family kinases.|
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|PMID: 23143416 Owner: NLM Status: MEDLINE|
|Protein kinases, key regulators of intracellular signal transduction, have emerged as an important class of drug targets. Chemical proteomic tools that facilitate the functional interrogation of protein kinase active sites are powerful reagents for studying the regulation of this large enzyme family and performing inhibitor selectivity screens. Here we describe a new crosslinking strategy that enables rapid and quantitative profiling of protein kinase active sites in lysates and live cells. Applying this methodology to the SRC-family kinases (SFKs) SRC and HCK led to the identification of a series of conformation-specific, ATP-competitive inhibitors that have a distinct preference for the autoinhibited forms of these kinases. Furthermore, we show that ligands that have this selectivity are able to modulate the ability of the regulatory domains of SRC and HCK to engage in intermolecular binding interactions. These studies provide insight into the regulation of this important family of tyrosine kinases.|
|Ratika Krishnamurty; Jennifer L Brigham; Stephen E Leonard; Pratistha Ranjitkar; Eric T Larson; Edward J Dale; Ethan A Merritt; Dustin J Maly|
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|Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't Date: 2012-11-11|
|Title: Nature chemical biology Volume: 9 ISSN: 1552-4469 ISO Abbreviation: Nat. Chem. Biol. Publication Date: 2013 Jan|
|Created Date: 2012-12-14 Completed Date: 2013-02-04 Revised Date: 2013-08-15|
Medline Journal Info:
|Nlm Unique ID: 101231976 Medline TA: Nat Chem Biol Country: United States|
|Languages: eng Pagination: 43-50 Citation Subset: IM|
|Department of Chemistry, University of Washington, Seattle, Washington, USA.|
|Data Bank Information|
Bank Name/Acc. No.:
|PubChem-Substance/152146113; 152146114; 152146115; 152146116; 152146117; 152146118; 152146119; 152146120; 152146121; 152146122; 152146123; 152146124; 152146125; 152146126|
|APA/MLA Format Download EndNote Download BibTex|
src-Family Kinases / chemistry, metabolism*
|R01 AI089441/AI/NIAID NIH HHS; R01 GM086858/GM/NIGMS NIH HHS; R01AI089441/AI/NIAID NIH HHS; R01GM086858/GM/NIGMS NIH HHS|
|0/Photoaffinity Labels; 56-65-5/Adenosine Triphosphate; EC 126.96.36.199/src-Family Kinases|
Journal ID (nlm-journal-id): 101231976
Journal ID (pubmed-jr-id): 32624
Journal ID (nlm-ta): Nat Chem Biol
Journal ID (iso-abbrev): Nat. Chem. Biol.
nihms-submitted publication date: Day: 12 Month: 10 Year: 2012
Electronic publication date: Day: 11 Month: 11 Year: 2012
Print publication date: Month: 1 Year: 2013
pmc-release publication date: Day: 01 Month: 7 Year: 2013
Volume: 9 Issue: 1
First Page: 43 Last Page: 50
PubMed Id: 23143416
|Active site profiling reveals coupling between domains in SRC-family kinases|
|Jennifer L. Brigham1|
|Stephen E. Leonard1|
|Eric T. Larson2|
|Edward J. Dale1|
|Ethan A. Merritt2|
|Dustin J. Maly1*|
1Department of Chemistry, University of Washington. Seattle, WA 98195. U.S.A.
2Department of Biochemistry, University of Washington. Seattle, WA 98195. U.S.A.
|*Correspondence: firstname.lastname@example.org (Tel: 206-543-1653/ FAX: 206-685-7002)
Protein kinases are a large family of enzymes that mediate intracellular protein phosphorylation1. Spatial and temporal coordination of protein kinase activity is essential for proper cellular function. Therefore, it is not surprising that protein kinase misregulation leads to a variety of diseases including cancer, inflammation, and diabetes2. A correspondingly large percentage of drug discovery research focuses on kinase inhibitors as molecularly targeted drugs, with over a dozen successfully completing clinical trials3. Significant efforts have been made to investigate this large enzyme family, of which only a small percentage of its 518 members have been functionally analyzed. The functional annotation of enzymes in other large protein families has greatly benefited from the development of activity- and affinity-based probes that selectively target conserved active site features4,5. For example, activity-based fluorophosphonate probes have proven to be powerful reagents for uncovering potential new serine hydrolase drug targets and performing inhibitor selectivity screens in complex proteomes6. While a number of useful proteomic tools have been developed for studying protein kinases7–9, there remains a need for reagents that allow rapid and quantitative analysis of protein kinase active sites in their native biological environments.
In order to comprehensively profile the roles that protein kinases play in the cell, methods that facilitate interrogation of their ATP-binding sites irrespective of their functional or activation state are particularly useful. In this study, we detail the development and application of a new method for the intracellular labeling of protein kinases in complex biological mixtures. Our strategy relies on a cell-permeable, ATP-competitive photo-probe that covalently modifies the ATP-binding sites of protein kinases upon irradiation with ultraviolet (UV) light. This probe contains an orthogonal chemical handle that facilitates the rapid and quantitative profiling of protein kinase active sites in their native biological environments.
In this study, we have applied our labeling strategy to a family of multidomain, nonreceptor tyrosine kinases called the SRC-family kinases (SFKs). These kinases play important roles in mediating diverse signaling processes and are promising therapeutic targets for a number of diseases10,11. SFKs contain regulatory domains that modulate their catalytic phospho-transfer activity and cellular localization. A number of studies have revealed the structural and biochemical basis of the catalytic regulation of SFKs12,13. Despite this extensive characterization, how regulatory domain interactions influence the ability of the ATP-binding pocket to accommodate small-molecule ligands is not well understood. Using our labeling method, we have identified a series of ATP-competitive inhibitors that display distinct selectivity for the active sites of autoinhibited SFKs in vitro and in situ. Furthermore, by obtaining a structure of one of these inhibitors bound to the catalytic domain of SRC, we have identified the molecular determinants of this preference. Finally, we show that inhibitors that display a preference for autoinhibited SFKs modulate the ability of their regulatory domains to engage in intermolecular interactions. These studies provide insight into how inhibitors can be designed to modulate interactions outside of the ATP-binding site of this therapeutically important enzyme family.
We identified three necessary components for developing general probes that can be used to profile the functional states of protein kinases in complex protein mixtures: (i) a general ligand that can direct a probe to the active site of protein kinases, (ii) a reactive moiety that allows the covalent labeling of bound kinase active sites, and (iii) a chemo-selective tag for conjugation to a reporter. For our studies, the cancer drug dasatinib was selected as the directing group due to its broad kinase target profile. Chemical proteomics studies have determined that dasatinib targets over 40 kinases, including many of clinical interest7,14–16. Furthermore, the interaction of this drug with kinases has been both biochemically and structurally characterized, so it can be derivatized without affecting potency or selectivity16–18. In order to allow covalent labeling of bound kinase active sites, the piperazine moiety of dasatinib was modified with a photo-reactive benzophenone photo-crosslinker (Fig. 1a). Although a number of chemoselective tags can be used to detect labeled kinase targets19, we wished to develop a method that allows rapid and quantitative determination of crosslinking efficiency in a single experiment using immunoblotting as a readout. To do this, an orthogonal chemical handle hexylchloride, which is able to undergo a rapid and selective reaction with the self-labeling protein HaloTag, was incorporated into our probe (1, Fig. 1b)20. The ability to selectively conjugate a large protein to labeled kinases allows for photo-crosslinking efficiency to be determined with a ratiometric gel-shift assay (Supplementary Results, Supplementary Fig. 1).
Prior to performing labeling reactions with 1, we determined whether our modifications affected the capacity of dasatinib to interact with its kinase targets. As expected, 1 retained the ability to potently inhibit the kinases that it was tested against (Supplementary Table 1). Next, the crosslinking efficiency of hexylchloride probe 1 was determined using two different sets of reaction conditions. In the pre-conjugation method, 1 is conjugated to the active site of HaloTag prior to performing photo-crosslinking experiments. The HaloTag-1 conjugate, HT-1, is then incubated with a protein mixture and inhibitor-bound kinases are labeled upon irradiation with UV light (Fig. 1c and Supplementary Fig. 2). In the post-conjugation method, 1 is first photo-crosslinked to inhibitor-bound targets and labeled proteins are subsequently conjugated to HaloTag. For both methods, the percentage of labeled kinase can be determined by separating UV-irradiated samples on an SDS-PAGE gel and probing with a kinase-specific antibody. This results in two distinct bands: a band corresponding to the unlabeled kinase and a mass-shifted band corresponding to the crosslinked kinase conjugated to HaloTag (Supplementary Fig. 1). The efficiency of each method was compared by performing crosslinking experiments with recombinant SRC that had been added to mammalian cell lysates (Fig. 1d and Supplementary Fig. 3). At least 50% of SRC was photo-crosslinked when 1 was conjugated to HaloTag prior to UV irradiation (Fig. 1d), with labeling remaining linear for up to 30 minutes (Supplementary Fig. 4). A similar crosslinking efficiency was observed for the SFK HCK. For both kinases, the absence of a higher molecular weight complex in the presence of an excess of active site competitor demonstrates that the crosslinking event is dependent upon active site binding. In contrast, the post-conjugation method was found to give a much lower crosslinking efficiency (Supplementary Fig. 3). Based on these results, all further experiments were carried out with the pre-conjugation method.
We next determined if our probe was able to efficiently label endogenous protein kinases in mammalian cell lysates. The HT-1 conjugate was incubated with COS-7 cell lysate and then irradiated with UV light. Immunoblotting with an α-SFK antibody demonstrated that greater than 50% of the endogenous SFKs were labeled. (Fig. 2a) A similar crosslinking efficiency (~30%) was observed in HeLa cell lysate (Fig. 2a). Next, the ability of 1 to label kinases in live cells was explored. COS-7 cells transiently expressing HaloTag were treated with probe 1 (Fig. 2b). After incubation and irradiation, the amount of photo-crosslinked SRC was determined. Under these conditions, a mass-shifted band corresponding to the kinase-HaloTag conjugate was observed. For cells that were also incubated with a competitor, no crosslinked kinase was observed. Kinase crosslinking in cells was also found to be UV light dependent (Supplementary Fig. 5) and linear with irradiation time (Supplementary Fig. 6). These results demonstrate that 1 is able to efficiently label endogenous kinases in live cells.
The ability of 1 to efficiently label individual nonreceptor tyrosine kinases in cells was next determined. The SFKs SRC, HCK, LCK, FGR, and BLK and the Tec-family kinase BTK were co-transfected with HaloTag into COS-7 cells. HaloTag-expressing cells were incubated with 1, followed by UV irradiation. Under these conditions, 1 labeled all of the kinases tested (Fig. 2c and Supplementary Fig. 7). Remarkably, 37% and 14% of total intracellular SRC and HCK were labeled by HT-1, respectively. Although LCK, FGR, BLK, and BTK were not labeled as efficiently, the amount of crosslinking observed is sufficient for intracellular profiling of these kinases. The absence of a mass-shifted band for crosslinking experiments performed in the presence of a dasatinib competitor demonstrated that labeling was active site-dependent (Supplementary Fig. 7). Furthermore, introduction of an ATP-binding site mutation, SRCT338I, which disrupted dasatinib binding16, prevented active site labeling (Fig. 2c).
Most protein kinases within the cell possess low catalytic activity in the absence of external stimuli. These enzymes are activated in response to signaling events through a number of mechanisms12,21. Activation causes conformational changes that align key catalytic residues in the ATP-binding site. In SFKs, the catalytic activity of the ATP-binding site is controlled by intramolecular regulatory domain interactions12,13,22. These multidomain proteins contain SH2 and SH3 regulatory domains at the N terminus and a C-terminal catalytic kinase domain. Intramolecular engagement of the SH2 and SH3 domains clamps the kinase in a catalytically inactive conformation. Release of these intramolecular interactions leads to activation of the catalytic domain. Despite extensive study of these regulatory interactions, it is still unclear how these events affect the conformation of the ATP-binding sites of SFKs.
The active sites of protein kinases can sample multiple conformational states, and a photo-affinity probe that does not rely on catalytic activity has the potential to profile all of them. Therefore, we determined the ability of 1 to profile SFKs across a range of activation states. To this end, a panel of SRC and HCK constructs was assembled. A series of mutations outside the active sites of SRC and HCK were selected; each set of mutations biased these kinases towards a specific activation state (Fig. 3a; SRC residue numbering is used to identify each of the various mutations). Highly activated SRC and HCK constructs, SRCAct and HCKAct, contain mutations that disrupt the interaction of the SH2 linker and SH3 domain as well as convert Tyr527 to a nonphosphorylatable phenylalanine. These constructs preclude intramolecular binding and allow the kinase to adopt an activated state23,24. SRC and HCK variants of intermediate activity were generated by mutating tyrosine residues that are regulated by phosphorylation to phenylalanines (Y416F or Y527F). Mutating Tyr527 to a phenylalanine (Y527F) considerably weakened SH2-domain binding because the unmodified C-terminal tail is a suboptimal ligand for this domain. Y416F removes the activation loop residue that is phosphorylated in SFKs25. In addition, two variants that cause SFKs to adopt a closed conformation, and therefore possess low catalytic activity, were generated. The SH3 domain-engaged SFK constructs, SRCSH3eng and HCKSH3eng, are autoinhibited because the introduction of multiple prolines into the SH2 linker enhances the affinity of the SH3 domain for this segment26. The SH2 domain-engaged SFK constructs, SRCSH2eng and HCKSH2eng, contain a C-terminal tail that is a high affinity ligand for the SH2 domain independent of Tyr527 phosphorylation27–30. Prior to performing labeling experiments, each construct was transiently expressed in COS-7 cells and the level of activation loop phosphorylation was determined with a phospho-Y416-specific antibody (Fig. 3b). The relative amounts of phosphorylation are consistent with the engineered regulatory preferences of these constructs.
The ability of 1 to label the active sites of the constructs described above was determined in COS-7 cells. Photo-crosslinking experiments were performed. Interestingly, 1 labeled each series of SFK constructs with almost equal efficiency, regardless of the activation state (Fig. 3c and Supplementary Fig. 8). All of the SRC constructs were labeled with comparable efficiency (35–45%). The HCK variants followed a similar trend, with a crosslinking efficiency of 11–17%. These results are consistent with a study that demonstrated that dasatinib had a similar affinities for unactivated and activation loop-phosphorylated ABL31.
From previous studies of SFK activity and regulation, it has been established that (i) SFKs adopt several different ATP-binding site conformations and (ii) regulatory domain interactions control the catalytic activity of this kinase family. We sought to examine the interplay between these sites in a physiologically relevant context with 1. To do this, we assembled a series of ATP-competitive SRC and HCK inhibitors to determine whether any of these ligands displayed a preference for the distinct active or autoinhibited states (Fig. 4a). The capacity of 1 to label multiple activation states with equal efficiency provided us with a means to rapidly profile each inhibitor in a competition assay. Prior to testing our panel of HCK and SRC inhibitors in cells, their abilities to compete with 1 for ATP-binding site labeling was determined with purified SRC and HCK constructs in vitro. HCKSH3eng, HCKSH2eng, and SRCSH2eng, which contain intramolecularly engaged regulatory domains, were tested. Activated phospho-isoforms of SRC and HCK, generated via auto-phosphorylation of the activation loop of SRCY527F and HCKY527F, were also screened (Supplementary Fig. 9). To allow quantitative and rapid determination of crosslinking inhibition, a fluorescently-labeled HT-1 construct was used.
In total, nine SFK inhibitors were profiled against the purified SFK variants described above (Fig. 4a and Table 1). Several of the inhibitors tested (2, 8–10) were more effective competitors of the autoinhibited HCK constructs (HCKSH3eng and HCKSH2eng) than activated HCK. A similar trend was observed with inhibitors 8–10 for the SRC variants. Interestingly, several inhibitors displayed divergent effects on SRC and HCK. For example, 3 and 6 more effectively competed for crosslinking to SRCAct than SRCSH2eng but had little preference for any of the HCK variants. Inhibitors based on the pyrazolopyrimidine scaffold (6–10) demonstrated some of the most interesting differences in the competition assays for the HCK and SRC constructs (Table 1). Inhibitors that contained smaller aryl substituents at the C-3 position of the pyrazolopyrimidine core (6 and 7) were almost equally potent competitors for the activated and autoinhibited SFK variants. In contrast, analogs that contained larger aryl groups at the C-3 position (8–10) demonstrated a striking preference for autoinhibited SRC and HCK constructs over their activated forms. For example, inhibitor 8 competed 57- and 90-fold more effectively for HCKSH2eng and HCKSH3eng than for activated HCK, respectively. Similarly, inhibitors 9 and 10 showed a distinct preference for the ATP-binding sites of autoinhibited SRC and HCK over SRCAct and HCKAct. To confirm these trends, inhibitors 7–10 were tested in an in vitro activity assay against activated and autoinhibited SRC and HCK constructs (Supplementary Fig. 10). Consistent with the results of the photo-crosslinking competition experiments, inhibitors 8–10 had significantly lower Kis for the autoinhibited forms of SRC and HCK. Furthermore, 7, which had a similar IC50 for all of the SFK constructs in the photo-crosslinking competition experiments, was an almost equipotent inhibitor of all of the SFK constructs.
To determine whether pyrazolopyrimidine ligands demonstrated the same selectivity trend in a more physiologically relevant environment, cellular competition assays were performed to obtain in situ IC50 values. To do this, crosslinking experiments were performed in COS-7 cells with variable concentrations of dasatinib or 10 as competitors. Competition experiments were performed with the highly activated SFK constructs, SRCAct and HCKAct, and their autoinhibited analogs SRCSH3eng and HCKSH3eng. After irradiation, the extent of competition at each inhibitor concentration was determined via immunoblotting (Supplementary Fig. 11). 10 produced the same trend with SRC and HCK in situ as it did in the in vitro competition experiments. This inhibitor is at least 70-fold more potent in the cellular competition assay against HCKSH3eng over HCKAct (Fig. 4b and Supplementary Fig. 12). In cells, 10 did not show significant competition for SRCAct at the highest concentration tested (3 µM) but competed effectively for the autoinhibited form of SRC (SRCSH3eng).
Due to the distinct binding preferences of inhibitors 8–10 for autoinhibited forms of SRC and HCK, we sought to understand how this class of ligands interacts with the ATP-binding sites of SFKs. To this end, we obtained a crystal structure of 9 bound to the catalytic domain of SRC (Fig. 5 and Supplementary Fig. 13). Two molecules of unphosphorylated SRC kinase domain bound to 9 were observed per crystallographic asymmetric unit. As expected, inhibitor 9 occupied the ATP-binding site of SRC, making many of the same interactions as the adenine ring of ATP. Interestingly, the catalytic domain of 9 adopted the SRC/CDK-like inactive conformation32–34. This inactive conformation is characterized by movement of helix αC in the N-terminal lobe, with the rotation of a conserved, catalytically-important glutamic acid residue (Glu310) (Fig. 5b, c). The chlorobenzyloxy group at the C-3 position of the pyrazolopryimidine scaffold projected into the pocket created by the movement of helix αC. Although the chlorobenzyloxy groups adopted slightly different conformations in the two complexes, in both cases an overlay of the inhibitor 9-SRC complex with a crystal structure of active SRC showed that the bulky aryl group would not be accommodated by the active form of the enzyme (Fig. 5d). Our crystallographic observations show that pyrazolopyrimidine inhibitors with extended substituents at the C-3 position stabilize the SRC/CDK-like inactive conformation of SFK ATP-binding sites.
Our competition results demonstrate that certain classes of inhibitors have higher affinities for auto-inhibited SRC and HCK constructs, while others do not. Thus, regulatory interactions affect the conformation of SFK active sites. We were curious whether stabilizing the ATP-binding sites of SFKs in a specific conformation would affect the ability of their regulatory domains to engage in intermolecular interactions. Inhibitors 8–10 were tested for their capacity to modulate the intermolecular accessibility of the SH3 domains of SRC and HCK (Supplementary Fig. 14). SH3 domain pull-down experiments with a polyproline (PP) peptide ligand were performed with SRCY527F and HCKY527F in the presence of saturating amounts of various inhibitors (Fig. 6a). In the presence of dasatinib, 22% and 27% of SRCY527F and HCKY527F were retained on the beads, respectively (Fig. 6b and Supplementary Fig. 15). In contrast, little to no SRCY527F or HCKY527F was pulled down when these SFKs were bound to inhibitors 8–10. Similar amounts of the isolated SH3 domain of HCK were retained on the beads when pull-down experiments were performed in the presence of dasatinib, 9 or 10, demonstrating that the observed differences in SH3 domain accessibility are due to ATP-binding site interactions (Supplementary Fig. 16). The diminished capacity of the SH3 domains of SRC and HCK to engage in intermolecular interactions when bound to inhibitor 10 was confirmed with a quantitative binding assay (Supplementary Fig. 17). The binding affinities of the SH3 domains of SRCY527F-10 and HCKY527F-10 for a fluorescently-labeled PP ligand was at least 10-fold lower than for SRCY527F-dasatinib and HCKY527F-dasatinib. Divergent behavior was observed for inhibitor 2 in the pull-down assay. Consistent with the preference that 2 demonstrates for autoinhibited HCK constructs, the SH3 domain of the HCKY527F-2 complex was hindered in its ability to engage an intermolecular PP ligand (Fig. 6b and Supplementary Fig. 15). However, when SRCY527F was bound to 2, a majority of its SH3 domain was accessible to an intermolecular SH3 ligand, which is consistent with the modest preference that this inhibitor shows in crosslinking competition assays for activated SRC. These pull-down experiments clearly demonstrate that the intermolecular accessibility of SFK regulatory interactions can be modulated through their ATP-binding sites.
In this study, we describe a new method for quantitatively analyzing the ATP-binding site occupancies of protein kinases in cell lysates and live cells. This methodology utilizes a probe, 1, that can be used to covalently label the active sites of protein kinases. The incorporation of a hexylchloride group allows the efficiency of the photo-crosslinking event to be determined ratiometrically. Although we have applied this methodology to protein kinases, this strategy should be applicable to any small-molecule probe that can be modified with an appropriate linker. This should allow for the development of quantitative labeling tools for the analysis of a number of protein families. The ability to apply 1 to quantitatively and efficiently profile kinase active site accessibility in physiologically relevant environments has proved useful for studying SFKs. Specifically, we determined how regulatory domain interactions influence the conformation of the ATP-binding sites of SRC and HCK. We were able to identify several inhibitors (8–10) that were selective for the autoinhibited forms of these SRC and HCK kinases. Although this screen could have been performed with any method that allows the ATP-binding site occupancies of SFK constructs with variable activation states to be determined, our labeling strategy was particularly well suited for this task.
To determine whether the observed preferences of inhibitors 8–10 for auto-inhibited SRC and HCK variants can be explained by the conformation of their ATP-binding sites when bound to these ligands, we obtained a crystal structure of 9 in complex with the catalytic domain of SRC (Fig. 5a). Interestingly, SRC was in the SRC/CDK-like inactive conformation. This conformation is characterized by the movement and rotation of helix αC in the N-terminal lobe of the catalytic domain, which disrupts a salt bridge between Glu310 in helix αC and a conserved catalytic lysine (Lys295) (Fig. 5b). The ATP-binding site of SRC in the SRC-9 complex is distinct from the inactive form, called the DFG-out conformation, that the tyrosine kinase ABL adopts when bound to the drug imatinib35. With one exception, all previous structures of isolated SFK catalytic domains have been in either the active or the DFG-out conformation32,36–38. Generally, the SRC/CDK-like inactive conformation has only been observed in autoinhibited SFK constructs that contain SH2 and SH3 regulatory domains33,34.
The SRC/CDK-like conformation has been observed for a number of kinases21. For example, the receptor tyrosine kinase EGFR adopts the SRC/CDK-like inactive conformation when bound to the drug lapatinib39. Directly relevant to our observations, the kinase domain of Bruton’s tyrosine kinase (BTK) displays ligand-induced conformational changes when bound to pyrazolopyrimidine inhibitor 10 and the ATP-binding site is in the SRC/CDK-like conformation40. Superposition of BTK bound to 10 and SRC bound to 9 showed that their ATP-binding sites are nearly identical in the presence of these inhibitors, with helix αC undergoing a similar degree of movement and rotation (Supplementary Fig. 18a). Inhibitor 10 would not be accommodated in the active form of BTK without this movement. Superposition of inhibitor 10 with the active form of SRC shows that a similar steric clash would be predicted to occur with helix αC (Supplementary Fig. 18b).
We hypothesized that stabilizing the SRC/CDK-like inactive conformation of SRC and HCK with ATP-competitive inhibitors would influence their regulatory domains. Consistent with our speculation, there was a direct correlation between an inhibitor’s preference for autoinhibited SFK constructs and its ability to induce an inaccessible SH3 domain. Inhibitors 8–10 hinder the intermolecular interactions between the SH3 domains of these kinases with a PP peptide ligand. Presumably this occurs because the SH3 domain’s intramolecular interaction with the SH2 linker is strengthened. These results show that ATP-competitive inhibitors that stabilize the ATP-binding site in distinct conformations influence distal regulatory domains.
These results have direct implications for the pharmacological inhibition of multidomain protein kinases like the SFKs. Many multidomain protein kinases use their regulatory domains to engage other signaling partners in the cell, often recruiting their catalytic domains to activated signaling complexes. Inhibitors, like 8–10, that stabilize an inactive ATP-binding site conformation and promote the intramolecular engagement of regulatory interactions would be predicted to prevent kinases from being recruited to active signaling complexes. This is in contrast to several recently reported examples of ATP-competitive kinase inhibitors that lead to activation or priming of specific signaling pathways41–43. Furthermore, while kinase phospho-transfer activity is essential for a variety of cellular processes, growing evidence suggests that these enzymes possess a number of important noncatalytic functions44. Protein kinases mediate protein scaffolding complexes, allosterically regulate other enzymes, and modulate protein-protein and protein-DNA interactions through mechanisms independent of their enzymatic activity. For example, the SH2 and SH3 domains of SRC allow this kinase to play important noncatalytic functions in integrin signaling and the formation of focal adhesions45. In SRC-deficient fibroblasts, kinase dead SRC mutants can rescue cell spreading on fibronectin to comparable levels as the wild-type protein. SFKs have also been shown to have other noncatalytic roles in JAK2 signaling, antigen-specific T-cell activation, and in B-cell antigen receptor signaling46–48. Beyond the SFKs, a large number of protein kinases contain additional domains that play important roles in both the catalytic and noncatalytic functions of these enzymes. The use of conformation-specific ATP-competitive inhibitors provides the opportunity to control the noncatalytic functions of protein kinases by modulating their abilities to engage in intermolecular protein-protein interactions. Thus, it may be possible to obtain different phenotypic effects through the ATP-competitive inhibition of the same kinase, simply by varying how an inhibitor interacts with the ATP-binding site. Finally, ATP-competitive inhibitors that modulate interactions outside of kinase active sites may allow for the differential regulation of the large number of pseudokinases, which are predicted to lack catalytic activity, encoded by the human genome.49 Chemical proteomic tools similar to those described in this study should aid in the discovery of pharmacological agents with these interesting properties.
Synthesis and characterization of probes are described in the Supplementary Methods.
SRC-family kinases SRC (residues 84–533) and HCK (residues 84–531) were expressed and purified as previously described50. Mutations were introduced into SRC and HCK by site-directed mutagenesis and were verified by DNA sequencing. SFKAct variants contained the following mutations (SRC residue numbering is used to identify each of the various mutations): SRC (K249E/P250E/Y527F) and HCK (P250A/P253A/Y527F). SFKSH3eng variants contained the following mutations: SRC (K249P/Q252P/T253P) and HCK (K249P/K252P). SFKSH2eng variants contained the following mutations: SRC (Q528E/P529E/G530I) and HCK (Q528E/Q529E/Q530I). Mutant SRC and HCK constructs were expressed and purified following the same procedure.
Purified kinase (100 nM), mammalian lysate (0.5 mg/ml) and HT-1 (500 nM) were diluted in PBS in a 96-well, U-bottom plate. Samples were prepared either in the absence or presence of 10 µM dasatinib. Samples were mixed and irradiated on ice at 365 nm for 30 minutes by placing a Spectroline ENF-260C UV lamp directly on top of the plate. After irradiation, 25 µL of 3X SDS loading buffer was added. Samples were separated by SDS-PAGE and visualized via Western blot using a non-phospho-SFK (Tyr416) (7G9) antibody (Cell Signaling). The scanned blots were quantified with LI-COR Odyssey software (mean ± SEM, n = 3). To determine the percent kinase crosslinked, the intensities of the mass-shifted band and the non-crosslinked kinase were measured. After background correction, the amount of crosslinked protein was calculated as the percentage of mass-shifted kinase over the amount of total kinase (sum of the mass-shifted and non-crosslinked kinase signals).
Purified kinase (25 nM), mammalian lysate (0.2 mg/ml), and HT-1 (150 nM) were diluted in PBS in a 96-well, U-bottom plate. The ATP-competitive inhibitor (3-fold dilutions over 9 wells) was added to the kinase mixture, and the plate was incubated at room temperature for 20 minutes prior to photo-crosslinking. Samples were mixed and irradiated on ice at 365 nm for 30 minutes by placing a Spectroline ENF-260C UV lamp directly on top of the plate. After irradiation, DTT (1 mM) and a fluorescein-tag (500 nM) were added. Samples were incubated at room temperature in the dark for one hour and quenched with 25 µl of 3X SDS loading buffer. Samples were separated by SDS-PAGE and visualized via in-gel fluorescence scanning using a GE Typhoon FLA 9000. The intensities of the mass shifted bands at each inhibitor concentration were quantified with ImageQuant. Data was analyzed using Prism Graphpad software and IC50 values were determined using non-linear regression analysis (mean ± SEM, n = 3). Inhibitors that were found to have an IC50 less than 25 nM were re-tested at lower concentrations of SRC and HCK.
All cells were grown at 37°C in high glucose DMEM supplemented with 10% FBS and streptomycin/penicillin. Cell culture protocol is detailed in the Supplementary Methods. COS-7 cells, grown in a 12-well plate, were co-transfected with a HaloTag fusion construct (pDest26) and the kinase of interest (pcDNA3.2-V5) using Fugene HD reagent (Promega). The cells were incubated at 37°C for 24 hours. The transfected cells were treated with 1 µM of 1 in 1 ml of media (high glucose DMEM, 10% FBS with Strep/Pen) for one hour at 37°C. The cells were then washed with media (3×, 5 minutes at 37°C) and then 1 ml of PBS was added. The cells were irradiated at 365 nm at 37°C for eight minutes by placing a Spectroline ENF-260C UV lamp directly on top of the uncovered plate. After irradiation, the PBS was aspirated and the cells were lysed with 1X SDS loading buffer containing PhosStop phosphatase inhibitor (Roche). Samples were separated on an SDS-PAGE gel and visualized via Western blot using an anti-V5 tag antibody (Sigma). The scanned blots were quantified with LI-COR Odyssey software to determine crosslinking efficiency (mean ± SEM, n = 3).
Formation of kinase-inhibitor complex: The kinase of interest (100 nM) and mammalian lysate (0.2 mg/ml) were diluted in immobilization buffer (50 mM Tris, 100 mM NaCl, 1 mM DTT, pH 7). The inhibitor of interest (5 µM) was added to this kinase dilution. DMSO was added to those samples that used no inhibitor. The mixture was allowed to incubate for 30 minutes prior to loading on the resin. Pull-down: 40 µl of a 50% slurry of SNAP-Capture Pull-down Resin (NEB) was placed in a microcentrifuge tube. The resin was washed (2×, 10 bed volumes) with immobilization buffer. A SNAP-tag-polyproline (PP) peptide fusion (VSLARRPLPPLP) (10 µM) was loaded onto the resin at a final volume of 100 µL in buffer. The resin was shaken at room temperature for 90 minutes, with agitation by a pipet every 15 minutes. After PP peptide immobilization, the resin was washed (2×, 10 bed volumes) and 100 µL of the kinase-inhibitor complex was loaded. The resin was allowed to shake at room temperature for one hour. After incubation with the kinase-inhibitor complex, the flow-through was collected and the resin washed (4×, 10 bed volumes). To elute the retained kinase, 100 µL of 1X SDS loading buffer was added and the beads were boiled at 90°C for 10 minutes. All samples were separated by SDS-PAGE and visualized via Western blot using an anti-His6 antibody (abm). The scanned blots were quantified with LI-COR Odyssey software to determine percent kinase retained on the resin based on the loaded and eluted fractions (mean ± SEM, n = 3).
All experiments were performed in triplicate, unless otherwise specified. Results are shown as mean ± standard error of the mean (SEM). Error bars represent ± SEM.
R.K. and D.J.M. conceived the idea and designed the study. R.K. conducted crosslinking experiments. R.K. and S.E.L. performed biochemical studies with SFK variants. R.K. and E.J.D. synthesized compounds. J.L.B. designed, expressed, and purified HaloTag fusion constructs. P.R. constructed, expressed, and purified SFK variants. E.T.L. and E.A.M. carried out crystallographic studies. R.K. and D.J.M wrote the paper.
FN2Competing Financial Interests: The authors declare no competing financial interests.
Several ATP-competitive inhibitors were kindly provided by R. Murphy (University of Washington, Seattle) and G. Perera (University of Washington, Seattle). This research was supported by the NIH: R01GM086858 (D.J.M) and R01AI089441 (E.A.M.); and the Alfred P. Sloan Foundation (D.J.M.)
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