Autophosphorylation of amino-acid residues is part of the folding process of various protein kinases. Conventional chemical screening of mature kinases has missed inhibitors that selectively interfere with the folding process. Here we report a cell-based assay that evaluates inhibition of a kinase at a transitional state during the folding process and identify a folding intermediate-selective inhibitor of dual-specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A), which we refer to as FINDY. FINDY suppresses intramolecular autophosphorylation of Ser97 in DYRK1A in cultured cells, leading to its degradation, but does not inhibit substrate phosphorylation catalysed by the mature kinase. FINDY also suppresses Ser97 autophosphorylation of recombinant DYRK1A, suggesting direct inhibition, and shows high selectivity for DYRK1A over other DYRK family members. In addition, FINDY rescues DYRK1A-induced developmental malformations in Xenopus laevis embryos. Our study demonstrates that transitional folding intermediates of protein kinases can be targeted by small molecules, and paves the way for developing novel types of kinase inhibitors.
Dysregulation of protein kinase activity has been implicated in pathological conditions, such as neurological disorders and tumorigenesis. The protein kinase family represents an attractive target for drug development1,2. Kinase inhibitors that target ATP-binding pockets sometimes cause adverse side effects by suppressing unintended kinases, because the sequence and structure of the pockets are well-conserved3. Innovative ideas are therefore necessary in drug discovery to obtain a highly selective inhibitor of the target kinase.
DYRK1A, dual-specificity tyrosine-phosphorylation-regulated kinase 1A, is a mammalian orthologue of Drosophila minibrain and is essential for brain development4. The physiological importance of DYRK1A has been suggested by its proposed relationship with various symptoms of Down syndrome (DS)5,6,7. DYRK1A resides within the obligate trisomic region of human chromosome 21 and the extra copy of the DYRK1A gene in people with DS causes a 1.5-fold increased expression of the dual-specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A) protein8. The excessive DYRK1A activity is not only pivotal in causing the characteristic facial features9,10 and congenital heart defects9 of DS, but is also associated with early-onset of Alzheimer’s disease11,12. The hypothesis that the elevated activity of DYRK1A contributes to these neurological disorders has stimulated an interest in DYRK1A as a potential target for therapeutic drugs4,12,13. In addition, inhibition of DYRK1A increases pancreatic β-cell proliferation, suggesting therapeutic promise for diabetes therapy14,15. To repress the excessive activity of DYRK1A, we had previously developed a synthetic small molecule, INDY, which potently suppresses the kinase activity of DYRK1A. INDY also inhibits other DYRK family members as well as Cdc2-like kinases16.
DYRKs and glycogen synthase kinase 3β (GSK3β) autophosphorylate their own tyrosine residue in their transitional state and phosphorylate serine or threonine residues on their substrates after maturation17,18,19,20,21. Lochhead et al. postulated the existence of a transitional intermediate of these kinases that has biochemical properties distinct from the mature state18,19. Interestingly, the intermediate showed different sensitivity to chemical inhibitors from the mature kinase. For example, the transitional intermediate of Drosophila DYRK2 was inhibited by Purvalanol A, but not by 4,5,6,7-tetrabromo-1H-benzotriazole (TBB), whereas the mature kinase was inhibited by both18. So far, selective inhibitors of the transitional intermediate have not yet been identified, because the focus of conventional drug screening has been on the mature forms of the kinases18,22.
Isolation of transitional intermediates is considered to be quite difficult because of their low population and short lifetimes23. Therefore, we developed a cell-based assay, named SPHINKS (substrate phosphorylation by sequential induction of kinase and substrate), to evaluate intermediate-selective inhibitors of DYRK1A. Through examination of our synthetic chemical library, we identified a small compound, referred to as FINDY (folding intermediate-selective inhibitor of DYRK1A), which interfered with the folding process of DYRK1A, but did not inhibit the substrate phosphorylation catalysed by the mature kinase. FINDY specifically suppressed autophosphorylation of Ser97 in DYRK1A, resulting in its degradation by proteasomes. Furthermore, we found that FINDY did not affect the kinase activity of the other members of the DYRK family, indicating the possibility that transitional intermediate-selective kinase inhibitors distinguish between the conserved family members.
Design of the cell-based assay targeting the intermediate
To evaluate intermediate-selective inhibitors of DYRK1A, we developed the SPHINKS assay, enabling us to evaluate kinase inhibition at the transitional state during the folding process (Fig. 1a). We first established a HEK293 cell line with dual-inducible expression of DYRK1A and TAU, a well-characterized substrate of DYRK1A24,25. Expression of FLAG-tagged DYRK1A (FLAG-DYRK1A) was controlled by the tet operator, and was initiated by treatment with doxycycline (Fig. 1b, lanes 4–6). TAU was expressed in a fused form with the destabilization domain FKBP12 (DD), which causes degradation of DD fusion proteins in the absence of a small molecule, Shield-1 (ref. 26). Treatment with Shield-1 for 2 h stabilized DD-TAU in a dose-dependent manner (Fig. 1b, lanes 2, 3, 5 and 6). Phosphorylation of the stabilized DD-TAU at Thr212 was enhanced 4 h after the administration of doxycycline (Fig. 1b, lanes 5 and 6; and Supplementary Fig. 1), indicating that DYRK1A is produced from the doxycycline-induced transcript within 4 h.
To distinguish kinase inhibition at the transitional state from that after maturation, we set up two types of time courses. Small molecules were administered either before the induction by doxycycline (time course: Tc 1) or after the accumulation of mature DYRK1A (Tc 2; Fig. 1a). Following additional incubation with Shield-1 for 2 h, total cell lysates were harvested, then subjected to western blot. If the compound selectively inhibits the transitional intermediate, but not the mature DYRK1A, it should suppress TAU phosphorylation in Tc 1, but not in Tc 2, as illustrated in Fig. 1a.
Identification of FINDY
Using the SPHINKS assay, we examined our chemical library and found a small molecule that suppressed TAU phosphorylation in Tc 1, but not in Tc 2 (Fig. 1c). This small molecule was referred to as FINDY (Fig. 1d). In contrast, the canonical DYRK1A inhibitor INDY suppressed TAU phosphorylation in both Tc 1 and 2 (Fig. 1c).
FINDY is structurally similar to an ATP-competitive inhibitor, RD0392 (Fig. 1e and Supplementary Fig. 2), which we identified through in vitro screening using recombinant DYRK1A. RD0392 bears a five-membered heterocyclic ring, rhodanine. This moiety has been reported as a substructure of Pan Assay Interference Compounds27, which are compounds that have frequently arisen as hits in high-throughput screening. Conversely, Mendgen et al. noted that small molecules bearing rhodanine are potentially valuable and should not be regarded as problematic or promiscuous binders per se28. Therefore, we synthesized structural derivatives of RD0392, one of which was FINDY.
In contrast to the dose-dependent inhibition by RD0392 and INDY in the in vitro assay, FINDY did not exert any observable inhibitory effect on the recombinant DYRK1A (Fig. 1f). This was supported by a computational docking simulation study, which showed that RD0392 was able to fit to the ATP-binding pocket of mature DYRK1A (Supplementary Fig. 3a,b), whereas FINDY could not (Supplementary Fig. 3c,d). FINDY decreased the amount of FLAG-DYRK1A in Tc 1, whereas DD-TAU and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) were unaffected. In contrast, the amount of FLAG-DYRK1A was unaltered in Tc 2 (Fig. 1c). These results suggest that FINDY selectively impairs the stability or translation of DYRK1A, leading to the suppression of TAU phosphorylation in Tc 1.
To determine whether the stability or the translation is affected by FINDY, we constructed a translation reporter system using ribosome skipping mediated by a 2A peptide. The 2A peptide inhibits normal peptide bond formation without affecting translation29, which enables the bicistronic expression of FLAG-DYRK1A and haemagglutinin (HA)-tagged enhanced green fluorescent protein (EGFP) (HA-EGFP) under the control of a doxycycline-driven promoter (Fig. 2a). When administered with doxycycline, FINDY decreased the amount of FLAG-DYRK1A in a dose-dependent manner (EC50 value: 2.2 μM), without affecting HA-EGFP (Fig. 2b). FINDY also decreased the amount of endogenous DYRK1A in a primary culture of cortical neurons (Fig. 2c). On the other hand, administration of RD0392 did not decrease the amount of FLAG-DYRK1A (Fig. 2d). Next, we examined the effect of FINDY on the degradation of FLAG-DYRK1A in the presence of a translation inhibitor, cycloheximide. Cells were pre-treated with doxycycline for 16 h, then incubated with cycloheximide and FINDY. Under this condition, FINDY did not induce the degradation of FLAG-DYRK1A compared with the vehicle treatment (Fig. 2e), indicating that FINDY destabilizes newly translated FLAG-DYRK1A.
FINDY suppresses autophosphorylation on Ser97 of DYRK1A
Catalytic activity of several protein kinases is regulated by autophosphorylation to stabilize the active conformation30. To investigate whether autophosphorylation is involved in the stabilization of DYRK1A, we prepared a substituted mutant with Arg (K188R) in place of Lys188. Lys188 in DYRK1A interacts directly with ATP; the substitution thus renders the kinase inactive, leading to a ‘kinase-dead’ mutant, which lacks autophosphorylation ability31. In our study, the K188R mutant protein of FLAG-DYRK1A was barely detected with western blot, whereas EGFP from the bicistronic cassette was detected (Fig. 3a, K188R). This suggests that the abrogation of autophosphorylation destabilizes the DYRK1A protein. To identify the residues required for the stabilization of DYRK1A, we mutated potential autophosphorylation sites. Ser97 and Tyr111 in the non-catalytic amino-terminal domain of DYRK1A can be autophosphorylated31. In addition, Tyr319 or Tyr321 in the activation loop are required to retain catalytic activity31,32,33, and the autophosphorylation of these residues has also been reported21. Similarly, the autophosphorylation of Ser520, which corresponds to Ser529 in the DYRK1A variant used in the present study, is required for its binding to 14-3-3β (ref. 34). Therefore, we prepared mutants with these residues substituted. The substituted mutant of S97A and the double mutant of Y321F/Y319F were degraded, whereas the other mutants remained (Fig. 3a), indicating that Ser97 and one of the tyrosine residues in the activation loop are required for the DYRK1A stabilization.
Ser97 and its surrounding amino-acid sequence in DYRK1A are highly conserved among various species (Fig. 3b), suggesting their functional importance. To detect phosphorylated Ser97 (p-Ser97), we generated a polyclonal antibody against p-Ser97, and transiently transfected 293T cells with the expression vectors of FLAG-DYRK1A and its mutants, in which the mutants were detectable, probably because the overexpressed proteins were beyond the capacity of proteasomal degradation. This antibody detected the intact DYRK1A (wild type, WT), but barely identified the kinase-dead (K188R) and S97A mutants in the western blot analysis (Fig. 3c). In addition, competition experiments using phospho- and non-phospho-peptides clearly confirmed the antibody’s specific recognition ability towards p-Ser97 (Supplementary Fig. 4). We then examined whether FINDY suppresses autophosphorylation. In the presence of FINDY, the amount of p-Ser97 significantly decreased, whereas signals for phosphorylated tyrosine residues (p-Tyr) were unaffected (Fig. 3d). In addition, mass spectrometry analysis of the trypsin-digested peptides of FLAG-DYRK1A showed that FINDY did not suppress the phosphorylation of Tyr321 in the activation loop (Supplementary Fig. 5). To confirm that the FINDY-mediated inhibition of Ser97 autophosphorylation is involved in degradation of DYRK1A, we examined whether FINDY destabilized the DYRK1A mutants of K188R and S97A, which were not able to catalyse Ser97 autophosphorylation. FINDY did not decrease the level of these mutants (Supplementary Fig. 6). Thus, FINDY acts as an inhibitor of the autophosphorylation and does not induce DYRK1A degradation by an independent mechanism. These results thus suggest that FINDY destabilizes DYRK1A by inhibiting Ser97 autophosphorylation.
To further determine whether Ser97 is autophosphorylated by an inter- or intramolecular mechanism, we generated HEK293 cells that co-expressed the kinase-dead K188R mutant (FLAG-DYRK1A K188R) and an intact DYRK1A fused with a DD tag (DD-FLAG-DYRK1A). If Ser97 autophosphorylation were mediated by an intermolecular mechanism, Ser97 of the kinase-dead K188R mutant would be phosphorylated when expressed in the presence of DD-FLAG-DYRK1A. However, we found that the overexpressed DD-FLAG-DYRK1A did not enhance the phosphorylation of Ser97 in the K188R mutant (Supplementary Fig. 7a). In addition, DD-FLAG-DYRK1A did not stabilize the co-expressed K188R protein (Supplementary Fig. 7b). These results suggest that the Ser97 autophosphorylation of DYRK1A is catalysed in an intramolecular manner. Furthermore, treatment with cantharidic acid, a protein phosphatase inhibitor, increased the amount of p-Ser97 signal in FLAG-DYRK1A (Supplementary Fig. 7c), suggesting that p-Ser97 is dephosphorylated by a phosphatase inhibited by cantharidic acid. Interestingly, the FLAG-DYRK1A protein, which was purified from HEK293 cells, did not significantly catalyse Ser97 autophosphorylation (Supplementary Fig. 7d,e). Consistently, FINDY did not decrease the levels of p-Ser97 in HEK293 cells when cells were treated with FINDY after the accumulation of mature DYRK1A (Fig. 3e). Taken together, these results suggest that Ser97 autophosphorylation is catalysed before maturation and that p-Ser97 is susceptible to dephosphorylation after maturation.
FINDY inhibits incorporation of biotin-ATP
We examined whether FINDY inhibited incorporation of ATP into the pocket of DYRK1A. An ATP analogue, the biotinylated acyl phosphate of ATP, which fits to the ATP-binding pocket of kinases, irreversibly reacts with the ATP-orienting lysine and transfers biotin to this lysine35. We applied this method in designing an experiment, which is illustrated in Fig. 4a. If FINDY occupies the ATP-binding pocket of the purified kinase, it would inhibit the binding of the biotin-ATP analogue to this region. FLAG-DYRK1A produced in the presence or absence of the small molecules was immunopurified from the cells. The biotinylation of the immunopurified FLAG-DYRK1A produced in the presence of FINDY was significantly suppressed compared with the vehicle control, whereas that of FLAG-DYRK1A produced with either INDY or RD0392 was not (Fig. 4b). This indicates that FINDY inhibits the incorporation of biotin-ATP into the DYRK1A intermediate during the folding process. As a positive control, treatment of the immunopurified FLAG-DYRK1A with 100 μM ATP before incubation with the biotin-ATP analogue blocked biotinylation (Fig. 4b).
Ser97 autophosphorylation in in vitro translation
To confirm the effect of FINDY on Ser97 autophosphorylation of DYRK1A in a simpler assay than living cells, we employed an Escherichia coli-based coupled in vitro transcription-translation system. The PURExpress system is reconstituted from recombinant proteins and purified ribosomes. The signal of p-Ser97 of DYRK1A was detected when expressed in the PURExpress system (Fig. 5a), indicating a possibility that Ser97 autophosphorylation does not require mammalian proteins. The band of p-Ser97 migrated slower than the major band of the FLAG-DYRK1A protein (Fig. 5a), indicating that a small portion of DYRK1A is autophosphorylated in this experiment. This suggests a low probability of the Ser97 autophosphorylation in the in vitro translation. We then performed the in vitro translation in the presence of FINDY or RD0392. FINDY and RD0392 suppressed Ser97 autophosphorylation in similar dosage ranges (Fig. 5b–d). In addition, FINDY did not inhibit substrate phosphorylation by the DYRK1A protein produced in the PURExpress system (Fig. 5e). In contrast, RD0392 inhibited substrate phosphorylation in a dose-dependent manner (Fig. 5e). We also examined tyrosine autophosphorylation of DYRK1A. In the PURExpress system, no significant effects of FINDY or RD0392 were observed on the signal from phosphorylated tyrosine (Supplementary Fig. 8). These results indicate that FINDY suppresses Ser97 autophosphorylation during the in vitro expression of DYRK1A.
We also confirmed whether the mature DYRK1A catalysed Ser97 autophosphorylation or not using the FLAG-DYRK1A protein produced in the PURExpress system. Immunopurified FLAG-DYRK1A bound on resin was reacted with lambda protein phosphatase, then allowed to autophosphorylate in the presence of ATP for 2 h. Consistent with the results using FLAG-DYRK1A purified from HEK293 cells (Supplementary Fig. 7d,e), the purified DYRK1A protein did not catalyse Ser97 autophosphorylation (Fig. 5f). Thus, Ser97 autophosphorylation is a one-off event during the translation or folding process. These results demonstrate that FINDY suppressed Ser97 autophosphorylation before the maturation of DYRK1A.
Ser97 autophosphorylation of recombinant DYRK1A proteins
To determine whether FINDY directly inhibits Ser97 autophosphorylation, we developed an in vitro autophosphorylation assay using a recombinant DYRK1A protein. DYRK1A fused with a GST-tag at the amino-terminus and with a Twin-Strep-tag (TS) at the carboxy-terminus (GST-DYRK1A-TS) was produced in E. coli cells at 6 °C to suppress autophosphorylation, as we found that the p-Ser97 signal decreased in cells cultured at low temperature (Supplementary Fig. 9a). GST-DYRK1A-TS was purified using tandem affinity purification with Strep-Tactin Sepharose followed by GSH-conjugating resin (Supplementary Fig. 9b), then subjected to an in vitro reaction with ATP (100 μM). Under these conditions, the p-Ser97 signal did not increase, whereas the protein band was broadly shifted (Fig. 6a,b). Therefore, we wondered if the incubation at 6 °C suppressed prior autophosphorylation of the tyrosine residues (Tyr319 and Tyr321) in the activation loop, which are required for Ser97 autophosphorylation (Supplementary Fig. 9c). To verify this possibility, we generated pseudo-phosphorylation mutants, in which these tyrosine residues were substituted for phosphomimetic aspartic or glutamic acid residues (Y319D, Y319E, Y321D and Y321E), then examined their facilitation of Ser97 autophosphorylation. The Y319D and Y319E mutants were purified (Supplementary Fig. 9d), whereas the Y321D and Y321E mutants formed aggregates. As expected, the Y319D and Y319E mutations facilitated Ser97 autophosphorylation of recombinant GST-DYRK1A-TS (Fig. 6a,b). Furthermore, the Y319E mutant catalysed substrate phosphorylation at an equivalent level to the WT kinase (Supplementary Fig. 9e).
We then examined the effect of FINDY on in vitro Ser97 autophosphorylation using the Y319E mutant. FINDY inhibited Ser97 autophosphorylation with an IC50 value of 110 nM, but did not suppress tyrosine phosphorylation (Fig. 6c,d), which is consistent with results in Fig. 3d. The FINDY-mediated inhibition of Ser97 autophosphorylation decreased due to competition with excess ATP (1 mM; Fig. 6d and Supplementary Fig. 9e). In contrast, the canonical inhibitor RD0392 suppressed both Ser97 and tyrosine phosphorylation in the Y319E mutant (Fig. 6e,f), with IC50 values of 205 and 514 nM, respectively. These results demonstrate that FINDY directly and selectively inhibits Ser97 autophosphorylation.
In addition, we examined whether or not FINDY inhibited substrate phosphorylation by these recombinant proteins. The in vitro kinase assay showed that FINDY did not inhibit substrate phosphorylation by the WT and Y319E proteins in concentrations of up to 16 μM (Fig. 6g). In contrast, RD0392 inhibited substrate phosphorylation by the WT and Y319E proteins with IC50 values of 325 and 813 nM, respectively (Fig. 6g).
FINDY strengthens interaction between DYRK1A and CDC37
Our recent study indicated that mutations affecting autophosphorylation strengthen the interaction between DYRK1A and the kinase-specific co-chaperone CDC37 (ref. 36). CDC37 assists in the folding of target kinases in cooperation with HSP90 (refs 37, 38). Taipale et al. have demonstrated that CDC37/HSP90 is associated with thermodynamically unstable kinases39 and that CDC37 fused with luciferase acts as a thermodynamic sensor for kinase structures40.
To investigate whether the mutation of Ser97 affects the thermodynamic stability of DYRK1A, we examined the interaction between the S97A mutant and CDC37 fused with luciferase nanoKAZ, as described in our recent study36, with some modifications (see the Methods for details). The S97A, Y321F, Y319F/Y321F and K188R mutations significantly strengthened the interaction of DYRK1A with CDC37-nanoKAZ (Fig. 7a). The S97A mutant interacted with CDC37-nanoKAZ 2.2-fold more strongly than intact DYRK1A (Fig. 7a). The Y321F, Y319F/Y321F and K188R mutants interacted 5.2-, 6.2- and 54-fold more strongly than intact DYRK1A, respectively (Fig. 7a). Interestingly, the Y321F mutation increased the interaction (Fig. 7a), but did not destabilize the DYRK1A protein in HEK293 cells (Fig. 3a). Thus, the increased interaction with CDC37 is not always correlated with the degradation of DYRK1A mutants. Therefore, another functional role of Ser97 may be involved in the degradation of DYRK1A.
We next investigated whether FINDY decreases the thermodynamic stability of DYRK1A. Treatment with FINDY significantly strengthened CDC37-nanoKAZ interactions in a dose-dependent manner, whereas treatment with RD0392 weakened the interactions (Fig. 7b), suggesting that FINDY induces thermodynamic destabilization of DYRK1A. In addition, we examined the effect of FINDY on the S97A mutant. FINDY also increased the CDC37 interaction with the S97A mutant, but it tended to be less than that with intact DYRK1A (Supplementary Fig. 10). These results suggest that FINDY affected a part of the folding process in a mechanism independent of the Ser97 autophosphorylation.
Selective inhibition of DYRK1A by FINDY
To determine the selectivity of FINDY, potential inhibitory activity was assessed against a panel of 275 kinases using 10 μM of FINDY. Only five other kinases (GSK3β, MARK4, PIM1, PIM3, PLK3) were inhibited by over 75% and none of these showed over 85% inhibition (Supplementary Table 1). In addition, FINDY did not exhibit any inhibitory effect on DYRK1B and DYRK2 in an in vitro kinase assay, whereas RD0392 inhibited both kinases in a dose-dependent manner (Fig. 8a,b). DYRK1B, the member of the DYRK family closest to DYRK1A, possesses a conserved serine residue similar to Ser97 of DYRK1A (Supplementary Fig. 11a), the mutation of which also leads to destabilization of DYRK1B (Supplementary Fig. 11b). Therefore, we investigated whether FINDY destabilizes DYRK1B and DYRK2 in cells expressing FLAG-DYRK1B-2A-EGFP and FLAG-DYRK2-2A-EGFP, respectively. Neither the expression of FLAG-DYRK1B nor FLAG-DYRK2 was affected by FINDY (Fig. 8c,d). These results suggest that the transitional intermediate of DYRK1A has a unique structural property distinct from that of DYRK1B and DYRK2. Moreover, FINDY decreased the amount of endogenous DYRK1A in HEK293 cells, whereas no alteration in the endogenous expression of the other 13 kinases was observed (Fig. 8e), indicating that FINDY selectively destabilizes the transitional intermediate of DYRK1A.
We have previously reported that microinjection of DYRK1A mRNA into Xenopus laevis embryos causes the malformation of neural tissues, and this system has been applied to assess the efficacy of kinase inhibitors in vivo16. To validate the subtype-selectivity of FINDY in the context of living organisms, we investigated whether FINDY rescues the developmental malformation of Xenopus embryos induced by the overexpression of DYRK1A or DYRK1B. DYRK1A or DYRK1B mRNA was injected into two dorsal blastomeres at the eight-cell stage, resulting in malformation of the eye and the head in stage 40 tadpoles (Fig. 9a). Control β-globin mRNA did not cause any morphological alterations compared with uninjected embryos (Fig. 9a). Administration of proINDY, which is an acetylated prodrug with enhanced cell membrane permeability hydrolysed in the cell to form INDY16, repressed the malformation induced by both DYRK1A and DYRK1B (Fig. 9a). FINDY rescued the malformation induced by DYRK1A, but not that induced by DYRK1B, demonstrating marked subtype-selectivity (Fig. 9a). Embryos injected with DYRK1A mRNA were almost completely rescued with the administration of either FINDY or proINDY (Fig. 9b). Only 10.9% of the tadpoles developed normally with FINDY when injected with DYRK1B mRNA, whereas 89.1% were normal in the presence of proINDY (Fig. 9b). In the embryos injected with either DYRK1A or DYRK1B mRNA, decreased expression of the pan-neural marker NCAM, forebrain marker BF-1, eye markers Pax-6 and Rx-1, fore-midbrain marker Otx-2, mid-hindbrain marker En-2 and hindbrain marker Krox-20 were observed (Fig. 9c). FINDY restored the expression of these markers only in DYRK1A-overexpressing tadpoles, whereas proINDY increased the expression of the markers in both DYRK1A- and DYRK1B-overexpressing embryos (Fig. 9c). These results indicate that FINDY rescues the neurological defects induced by DYRK1A in a highly specific manner.
This study provides methods for evaluating chemical compounds that selectively inhibit the transitional intermediates of target kinases. We utilized these methods to identify and evaluate FINDY. Based on the following evidence, we demonstrate that FINDY selectively inhibits a folding intermediate of DYRK1A during its folding process, as illustrated in Fig. 10. First, FINDY suppresses the substrate phosphorylation by DYRK1A only when it is administered before the induced expression (Fig. 1c). Second, neither in the cell-based nor in the in vitro assays is FINDY able to inhibit the substrate phosphorylation by the mature DYRK1A (Figs 1c,f, 5e and 6g). Third, FINDY suppressed Ser97 autophosphorylation in cells (Fig. 3d), in the in vitro translation (Fig. 5), and in the in vitro autophosphorylation assay with the recombinant protein (Fig. 6). The Ser97 autophosphorylation was a one-off intramolecular process that was not catalysed by the mature DYRK1A (Fig. 5f and Supplementary Fig. 7d,e). Furthermore, the CDC37-nanoKAZ interaction assay revealed that FINDY induces the thermodynamic destabilization of DYRK1A (Fig. 7b), suggesting that FINDY affects the folding state of DYRK1A.
Our study demonstrates that FINDY directly suppresses Ser97 autophosphorylation, as discussed below. First, FINDY suppressed Ser97 autophosphorylation in the in vitro translation system (Fig. 5), which contained only defined factors, but did not contain mammalian proteins. Second, FINDY suppressed the in vitro Ser97 autophosphorylation of the recombinant phosphomimetic mutant (Y319E) of DYRK1A, whereas tyrosine autophosphorylation was not suppressed by FINDY (Fig. 6 and Supplementary Fig. 5). These results are consistent with the results from the cellular assays (Fig. 3d). Several lines of evidence demonstrated that the mature DYRK1A was not able to catalyse Ser97 autophosphorylation (Figs 5f and 6a,b and Supplementary Fig. 7d,e). Thus, the kinase form that catalyses Ser97 autophosphorylation is not the mature form. Therefore, the recombinant Y319E probably reflects an aspect of the folding intermediate. Third, FINDY blocked the incorporation of biotin-ATP into DYRK1A (Fig. 4), indicating two possibilities. One is that FINDY occupies the ATP-binding pocket. The other is that FINDY affects the biotin-ATP incorporation by binding to an allosteric site, which may affect the ATP binding to the pocket. FINDY possesses the same polar groups of RD0392 that targets the ATP-binding pocket of DYRK1A (Supplementary Figs 2 and 3). Thus, the former scenario is most likely. The selectivity of FINDY for the Ser97 and tyrosine autophosphorylation suggests that the transitional state targeted by FINDY is distinct to that of tyrosine autophosphorylation. Further structural studies are necessary to conclude this discussion.
The phosphomimetics experiment suggested that the phosphorylated tyrosine residue in the activation loop is required for the subsequent Ser97 autophosphorylation (Fig. 6). Although intramolecular tyrosine autophosphorylation in the activation loop has been suggested to be a one-off inceptive event to achieve full activity during the co-translational folding process of Drosophila DYRKs17,19,41, it is controversial whether the autophosphorylation of these tyrosine residues is essential for the catalytic activity of mammalian DYRK1A21,33. The double mutation of Y321F/Y319F in the activation loop destabilized FLAG-DYRK1A, whereas a single mutation gave a much smaller effect (Fig. 3a). Our study indicates that the autophosphorylation of at least one of these tyrosine residues is required for Ser97 autophosphorylation, suggesting that Ser97 autophosphorylation acts as a quality control mechanism. It remains elusive how Ser97 autophosphorylation regulates the stability of DYRK1A and why Ser97 autophosphorylation is a one-off process. In comparison to the in vitro translation (Fig. 5a), we did not observe the faster migrating band corresponding to the Ser97 non-phosphorylated DYRK1A in the cultured mammalian cells, which may be subjected to degradation during the folding process. The actual amount of the Ser97 autophosphorylation during the folding process in mammalian cells also remains unclear.
Although RD0392 inhibited the Ser97 autophosphorylation in the in vitro translation experiment (Fig. 5c,d) and in the autophosphorylation assay using the recombinant DYRK1A protein (Fig. 6e,f), RD0392 did not decrease the FLAG-DYRK1A protein in the cultured cells (Fig. 2d). This discrepancy is possibly due to low cell membrane permeability of RD0392. FINDY has a hydrophobic trimethylsilyl group that may serve to enhance the cell membrane permeability compared with that of RD0392. RD0392 inhibited the Tyr autophosphorylation of the recombinant DYRK1A protein (Fig. 6e,f). In contrast, RD0392 did not inhibit the Tyr autophosphorylation in the in vitro translation (Supplementary Fig. 8c). This indicates the possibility that RD0392 is capable of inhibiting post-translational Tyr autophosphorylation, but co-translational Tyr autophosphorylation is resistant to RD0392.
An interesting point in the biotin-ATP experiment is that INDY and RD0392 failed to inhibit biotinylation, whereas FINDY, on the other hand, did not (Fig. 4b). The most likely explanation is that FINDY has a slower rate of dissociation (Koff) from the intermediate of DYRK1A than the Koffs that INDY and RD0392 have to the mature form. This slow Koff for FINDY may be due to thermodynamic destabilization by FINDY, which is distinct from the effects of INDY and RD0392. FINDY uniquely strengthened the interaction between DYRK1A and CDC37-nanoKAZ (Fig. 7b). In contrast, RD0392 and INDY weakened the interaction (Fig. 7b)36, which is in good agreement with previous reports that canonical kinase inhibitors weaken CDC37 interactions39,40,42. A previous study has demonstrated that CDC37 binding competes with ATP for the pocket of its client kinase42, suggesting that the enhanced binding of CDC37 plays a role in the suppression of the biotinylation. Furthermore, the thermodynamic destabilization caused by FINDY may also cause hydrophobic aggregation of the DYRK1A protein, which masks the pocket and prevents the incorporation of ATP. Thus, we consider that thermodynamic destabilization by FINDY may result in strong competition with the biotin-ATP.
The SPHINKS assay consists of cells expressing DYRK1A and its substrate fused with a DD tag and the detection of TAU phosphorylation. This assay was developed to evaluate the effect of chemical compounds on the folding process of DYRK1A; however, it is not suitable for high-throughput screening of large-scale chemical libraries. Thus, the SPHINKS assay should be utilized as a second or third screening assay for a small number of chemical compounds that were roughly selected from the library by a robust high-throughput assay. The in vitro translation and autophosphorylation assays would be better methods for developing high-throughput assays. Some small molecules may show apparent selectivity in the SPHINKS assay because of slower actions, such as low solubility, pro-drug activation or slow uptake into cells. Thus, the properties of small molecules should be carefully examined.
This study demonstrates that targeting transitional intermediates is a promising strategy for the development of novel kinase inhibitors. Intramolecular autophosphorylation in the activation loop has been demonstrated not only in DYRK1A, but also in other kinases, such as DYRK2 (ref. 19), GSK3β (ref. 18), ERKs43 and the Parkinson’s disease-associated kinase LRRK2 (refs 44, 45). In addition, autophosphorylation outside the activation loop has been reported in C-RAF46 and protein kinase A (PKA)47. We believe that intermediate-selective inhibitors for these kinases can be identified. The close structural similarity between the intermediate-selective inhibitors and the canonical inhibitors raises the possibility that canonical ATP-competitive kinase inhibitors can be converted to intermediate-selective inhibitors with only a slight modification of the common chemical scaffold (Supplementary Figs 12 and 13). Numerous compounds targeting various kinases have been rejected in in silico or in vitro drug screening, but some could potentially inhibit a transitional intermediate of the target kinase. The methods developed in this study can be utilized to reassess these compounds and provide opportunities to rediscover selective kinase inhibitors.
The dynamic state of the transitional intermediate may provide conformational diversity for the inhibitor-binding pocket. It is possible to purify the metastable intermediate of the DYRK1A protein produced in the presence of FINDY, as we have preliminarily tried in Figs 4 and 5. Further studies using biophysical techniques are necessary in order to analyse the intermediate state targeted by FINDY. Resolving the intermediate states of kinases would expand the chemical options available for the design of selective inhibitors.
Small molecules were prepared using standard synthetic procedures, as described in Supplementary Methods. INDY and proINDY were prepared as described previously16. These compounds were dissolved in dimethylsulphoxide (DMSO) at 10 mM as a stock solution. Calyculin A (Cell Signaling Technology), okadaic acid (Tocris Bioscience) and cantharidic acid (Abcam) were purchased. The polyclonal antibody against p-Ser97 was produced by immunizing rabbits with a synthetic phospho-peptide, C-PEG-PLRKLS*VDLIK, which was coupled to KLH via the free cysteine, with S* representing phosphoserine. The specific antibody was purified by phospho-peptide-conjugating resin followed by a subtraction step on a column containing non-phospho-peptide. The polyclonal antibody against p-Ser97 (1/2,000) and antibodies listed below were diluted with Can Gel Signal Immunoreaction Enhancer Solution (TOYOBO) in western blot analysis. Mouse monoclonal anti-DYKDDDDK (FLAG) tag (1/1,000, clone 1E6, 018-22381/Lot: CTR5949) and anti-GFP (1/1,000, mFX75, 012-22541/Lot: STK2113) antibodies were purchased from Wako Pure Chemical Industries, mouse monoclonal anti-HA (1/1,000, clone HA124, 06340-54/Lot: M2E8170) antibody from Nacalai Tesque, mouse monoclonal anti-GAPDH (1/10,000, clone 6C5, AM4300/Lot: 1311029) from Thermo Fisher Scientific, mouse monoclonal anti-TAU (1/3,000, clone TAU-5, 577801/Lot: D00100518) from Calbiochem (Merck), rabbit polyclonal antibody against pT212 of TAU (1/3,000, 44740G/Lot: 1392715A) from Life Technologies, mouse monoclonal anti-phosphotyrosine (1/3,000, 4G10 Platinum, 05-1050/Lot: 2567063) from Millipore, mouse monoclonal anti-GST-tag (1/3,000, clone GT5, M209-3/Lot: 001) from MBL, mouse monoclonal anti-SRPK1 (1/3,000, clone 12/SRPK1, 611072) from BD Transduction Laboratories (BD Biosciences), mouse monoclonal anti-CDK9 (1/3,000, clone D-7, sc-13130/Lot: c0613) from Santa Cruz Biotechnology and mouse monoclonal anti-neuronal class III β-Tubulin (1/3,000, clone TUJ1, MRB-435P/Lot: E10045BF) from Covance. Rabbit polyclonal anti-DYRK1A (1/3,000, #2771S/Lot: 1), p70S6K (1/3,000, #9202S/Lot: 8), CHK2 (1/3,000, #2662S/Lot: 5), MARK3 (1/3,000, #9311BC/Lot: 1), RAF1 (1/3,000, #9422BC/Lot: 5), FAK (1/3,000, #3285BC/Lot: 6), FYN (1/3,000, #4023BC/Lot: 2) and ABL (1/3,000, #2862BC/Lot: 11) antibodies were obtained from Cell Signaling Technology. Rabbit monoclonal anti-GSK3β (1/3,000, clone 27C10, #9315S/Lot: 4), AKT1 (1/3,000, clone C73H10, #2938BC/Lot: 2), MEK1 (1/3,000, clone 30C8, #9146BC/Lot: 1) and SRC (1/3,000, clone 32G6. #2123BC/Lot: 3) antibodies were purchased from Cell Signaling Technology. HRP-linked anti-rabbit (1/4,000, NA9340V/Lot: 9611780) and anti-mouse (1/4,000, ab5887/Lot: GR16899-9) IgG were purchased from GE Healthcare and Abcam, respectively. HRP-labelled streptavidin (1/2,000, 474-3000/Lot: 060065) was obtained from Kirkegaard & Perry Laboratories.
In brief, the bicistronic expression vectors for the DYRKs were constructed with pcDNA5/FRT/TO (Life Technologies). DD-TAU and DD-FLAG-DYRK1A were inserted into the pCAGIPuro vector. To prepare in vitro transcribed mRNAs for injection, DYRKs were inserted into the pCS2+ vector. pCold (Takara Bio) and pET28a(+) vectors were used for the preparation of recombinant protein in E. coli cells. The pET28a(+) vector was also used for the in vitro translation experiments. PCR-amplified fragments of the human microtubule-associated protein TAU (0N4R) and FLAG-tagged DYRK1A were fused in-frame to the carboxyl-terminus of DD tag by the overlap-extension PCR method to generate DD-TAU and DD-FLAG-DYRK1A, respectively, as described previously48, with some modifications. The combined fragments were inserted into the pCAGIPuro vector, an IRES-based bicistronic expression vector where the gene of interest and a puromycin-resistant gene are expressed from a single mRNA, which enables almost all of the cells selected with puromycin to express the gene product. A PCR-amplified fragment of FLAG-tagged DYRK1A was subcloned into pcDNA5/FRT/TO. For the bicistronic cassette using a 2A peptide, PCR-amplified fragments of FLAG-tagged DYRKs were fused in-frame to the amino-terminus of EGFP via the F2A peptide sequence by the overlap-extension PCR method. The combined fragments were inserted into pcDNA5/FRT/TO (Life Technologies). The site-directed mutagenesis of DYRK1A and DYRK1B was performed as described previously49, with some modifications. The reconstituted vector sequences are available upon request.
Cell culture and transfection
Flp-In/T-REx HEK293 (Life Technologies) and intact HEK293 cells were maintained in low-glucose DMEM (Nacalai Tesque) supplemented with 10% fetal bovine serum (FBS; Nichirei Biosciences), 100 U ml−1 of penicillin and 100 μg ml−1 of streptomycin (Nacalai Tesque). Cells were transfected with plasmid DNAs using polyethylenimine MAX (Polysciences) as described previously50, then selected with hygromycin B (Life Technologies) for the pcDNA5/FRT/TO vectors and/or with puromycin (Nacalai Tesque) for the pCAGIPuro vectors to establish stable cell lines.
Our original synthetic chemical library used in this study consisted of newly synthesized structural derivatives of ATP-competitive inhibitors of DYRK1A, which had been identified by an in vitro kinase assay in our laboratory. Flp-In/T-REx HEK293 cells transfected with pcDNA5/FRT/TO-FLAG-DYRK1A and pCAGIPuro-DD-TAU were seeded on polyethylenimine-coated six-well plates with 2 ml of DMEM and 1% FBS. Cells were then cultured 24 h later in the presence of 1 μg ml−1 of doxycycline (Nacalai Tesque) for 16 h, then treated with 1 μM of Shield-1 (Clontech, Takara Bio) for 2 h. Small molecules from our chemical library were diluted in 1 ml of DMEM and 1% FBS, then administered into the cells at a final concentration of 10 μM (0.1% DMSO), as illustrated in Fig. 1a. Total cell lysates were prepared with SDS-urea buffer (50 mM Tris-HCl, pH 7.0, 1% SDS, 4 M urea, 10% glycerol, 20 mM dithiothreitol, 0.5 mg ml−1 BSA), then analysed with SDS–polyacrylamide gel electrophoresis (SDS–PAGE) followed by western blot analysis using antibodies against phospho-TAU (pT212) (1/3,000) and total TAU (1/3,000) proteins (Supplementary Fig. 14). Details are summarized in Supplementary Table 2.
Immunoprecipitation of FLAG-DYRK1A
HEK293 cells were cultured in the presence of 1 μg ml−1 of doxycycline, 1 μM of Shield-1, 1 μM of epoxomicin and a proteasome inhibitor (Peptide Institute), with or without 10 μM of small molecules for 5 h. The cells were lysed in 50 mM Tris (pH 7.4), 150 mM NaCl, 0.5 mM EDTA, 1% Empigen BB and protease/phosphatase inhibitor cocktails (Nacalai Tesque). The clarified cell lysates were processed with anti-FLAG (clone M2) beads (F2426, Sigma-Aldrich) and the bound proteins were then eluted with SDS-urea buffer, then analysed with SDS–PAGE followed by western blot analysis (Supplementary Fig. 14).
Biotin transfer experiment
Biotinylation of the lysine in the ATP-binding pocket was performed using the Pierce Kinase Enrichment Kit with an ATP Probe (Thermo Fisher Scientific), according to the manufacturer's instructions with some modifications. HEK293 cells were cultured with 1 μg ml−1 of doxycycline and 1 μM of epoxomicin, with or without 10 μM of small molecules for 5 h, then harvested and lysed in Pierce IP Lysis Buffer containing 0.5% Empigen BB. The clarified cell lysates were processed with anti-FLAG (M2) beads, then equilibrated with the kit’s reaction buffer. The beads were subsequently reacted with 20 μM of the kit’s ActivX Desthiobiotin-ATP probe for 30 min at room temperature. The bound proteins were eluted with SDS-urea buffer, then analysed with SDS–PAGE followed by western blot analysis (Supplementary Fig. 14).
E. coli-based in vitro translation assay
The PURExpress kit (New England Biolabs) was employed. DYRK1A was expressed at 37 °C for 40 min in a 12.5-μl reaction mixture containing 30 ng of pET28a(+)-FLAG-DYRK1A. For inhibitor experiments, FINDY or RD0392 was added prior to the initiation of transcription. For immunoprecipitation, 100 μl of PBS containing 0.5% Empigen BB, 0.5 mg ml−1 BSA and 5 mM EDTA was added into the reaction mixture, then incubated with anti-FLAG (M2) beads at 4 °C for 6 h. The samples were prepared with an SDS-urea buffer, then analysed with SDS–PAGE followed by western blot (Supplementary Fig. 14). The band intensities were measured using the LAS-3000 (Fujifilm) and Multi Gauge software (Fujifilm).
For the phosphatase experiment, immunoprecipitated FLAG-DYRK1A bound on the beads was incubated in a total volume of 100 μl containing 1,600 U of lambda protein phosphatase for 2 h at 30 °C. After washing the beads with autophosphorylation reaction (AR) buffer (see below) containing 0.1 mg ml−1 of BSA (Sigma-Aldrich), the beads were incubated with the indicated concentrations of ATP and sodium orthovanadate (1 mM) for 2 h at 37 °C and prepared with the SDS-urea buffer. To check the residual phosphatase activity, non-treated immunoprecipitated FLAG-DYRK1A bound on the beads was added into the reaction.
For the in vitro kinase assay, 0.5 μl of the reaction mixture was incubated in a total volume of 25 μl of AR buffer containing 0.1 mg ml−1 of BSA, 100 μM of ATP, 50 μM of DYRKtide peptide (Anaspec) and the indicated concentrations of the small molecules for 2 h at 37 °C. The consumption of ATP was measured with ADP-Glo Kinase Assay kit (Promega Corporation).
In vitro autophosphorylation assays
E. coli strain Rosetta(DE3)pLysS was transformed with the pCold-I-GST-DYRK1A-TS vector. The cells were cultured with IPTG (final 1 mM) for 24 h at 6 °C, then lysed with GET buffer (20 mM HEPES-KOH, pH 8.0, 150 mM NaCl, 1 mM EDTA, 2 mM dithiothreitol, 10% glycerol, 0.5% Empigen BB, 0.5% Triton X-100). Clarified cell lysates were loaded onto a Strep-Tactin Sepharose column (IBA) and the bound proteins were then eluted with GET buffer containing 2.5 mM desthiobiotin (IBA) and 1 mg ml−1 BSA. The eluates were subsequently applied to GST-Accept resin (Nacalai Tesque). The resin was washed extensively, first with GET buffer, then with AR buffer (5 mM MOPS, pH7.2, 2.5 mM β-glycerol-phosphate, 5 mM MgCl2, 1 mM EGTA, 0.4 mM EDTA, 2 mM tris(2-carboxyethyl)phosphine). The GST-DYRK1A-TS (0.5 pmol) bound on the resin (bed vol. 2 μl) was suspended in 100 μl of AR buffer, mixed with 1 μl of a stock DMSO solution of FINDY or RD0392, then incubated at 37 °C for 30 min. We then added 5 μl of 2 mg ml−1 BSA to the suspension (final concentration of 0.1 mg ml−1), followed by incubation at 37 °C for 30 min. We then added 5 μl of ATP solution to the suspension (final concentrations of 100 μM and 1 mM), which was subsequently incubated at 37 °C for 2 h. The bound proteins were eluted with SDS-urea buffer, then analysed with SDS–PAGE followed by western blot (Supplementary Fig. 14).
The band intensities were measured using the ChemiDoc MP Imaging System (Bio-Rad). In Fig. 6d,e, the relative activity of the phosphorylation was calculated from the ATP-dependent increase in the intensity of the p-Ser97 and p-Tyr signals by subtracting the band intensity in the absence of ATP from that in the presence of ATP.
For the in vitro kinase assay, 2 μl (bed vol.) of the resin was incubated in a total volume of 25 μl of AR buffer containing 0.1 mg ml−1 of BSA, 100 μM of ATP, 50 μM of DYRKtide peptide and the indicated concentrations of the small molecules, for 2 h at 37 °C. The consumption of ATP was measured with ADP-Glo Kinase Assay kit.
CDC37-nanoKAZ interaction assay
The CDC37-nanoKAZ interaction assay was performed as described previously36, with some modifications. 293T cells stably expressing CDC37-nanoKAZ were transiently transfected with the expression vector 3xFLAG-DYRK1A, then cultured in a 96-well plate. Twenty-four hours after the transfection, FINDY and RD0392 were added to the wells at the indicated concentrations and the cells were cultured for an additional 24 h. The cells were lysed in ice-cold HENG buffer (50 mM HEPES-KOH, pH 7.9, 150 mM NaCl, 20 mM Na2MoO4, 2 mM EDTA, 5% glycerol, 0.5% Triton X-100) containing protease inhibitor cocktail (Nacalai Tesque) on ice. The cleared lysates were added to 96-well plates (OptiPlate-96 HB; Perkin Elmer) coated with antibody against FLAG peptide (clone M2, F3165/Lot: SLBH1191V) diluted in sodium bicarbonate buffer (pH 9.6), and incubated at 4 °C for 3 h. The wells were wash three times with ice-cold HENG buffer and then a luminescence assay was performed. The luminescence of the captured CDC37-nanoKAZ was measured using the Centro LB 960 Microplate Luminometer (Berthold Technologies). A reaction mixture containing bis-coelenterazine (final concentration of 0.1–1 μg in 100 μl) in PBS containing 0.02% Tween-20 and 20 mM EDTA was injected. The luminescence intensity was recorded at 0.1 s intervals for 10 s or 10 min. The maximum luminescence intensity (Imax), represented in relative luminescence units, was used in the study. The captured 3xFLAG-DYRK1A was also measured using HRP-conjugated anti-FLAG antibody (clone M2, A8592/Lot: SLBH1183V, Sigma-Aldrich) and TMD Super Sensitive One Component HRP Microwell Substrate (SurModics, Eden Prairie). The relative amount of protein bound on the well was estimated from the absorbance. The relative luminescence intensities were normalized to the amount of captured 3xFLAG-DYRK1A, and calculated as the fold-change relative to the value at 0 μM of the compounds.
Handling of Xenopus laevis embryos and reverse transcription (RT)–PCR analysis
DYRK1A and DYRK1B mRNA, which were synthesized from linearized vectors with the mMessage mMachine Kit (Life Technologies), were injected into two dorsal blastomeres at the eight-cell-stage for RT–PCR analysis and observation of the embryo phenotypes. Solutions containing proINDY or FINDY (2.5 μM each) were used to treat the embryos just after fertilization. The head regions of the injected embryos were dissected at the neural stage (stage 25) and the total RNA was isolated using TRIzol (Life Technologies). cDNA synthesis was carried out using Moloney murine leukaemia virus reverse transcriptase (Life Technologies). The sequences of the primer pairs were as follows51,52: NCAM, 5′-GCGGGTACCTTCTAATAGTCAC-3′ and 5′-GGCTTGGCTGTGGTTCTGAAGG-3′; Brain factor 1 (BF-1), 5′-TCAACAGCCTAATGCCTGAAGC-3′ and 5′-GCCGTCCACTTTCTTATCGTCG-3′; Pax-6, 5′-CAGAACATCTTTTACCCAGGA-3′ and 5′-ACTACTGCTAATGGGAATGTG-3′; Rx1, 5′-CCCCAACAGGAGCATTTAGAAGAC-3′ and 5′-AGGGCACTCATGGCAGAAGGTT-3′; Otx-2, 5′-GGATGGATTTGTTGCACCAGTC-3′ and 5′-CACTCTCCGAGCTCACTTCTC-3′; En-2, 5′-CGGAATTCATCAGGTCCGAGATC-3′ and 5′-GCGGATCCTTTGAAGTGGTCGCG-3′′; Krox-20, 5′-AACCGCCCCAGTAAGACC-3′ and 5′-GTGTCAGCCTGTCCTGTTAG-3′; ornithine decarboxylase (ODC), 5′-GTCAATGATGGAGTGTATGGATC-3′ and 5′-TCCATTCCGCTCTCCTGAGCAC-3′. No randomization was used, and no blinding was done.
HEK293 cells were cultured in the presence of 1 μg ml−1 doxycycline and 1 μM epoxomicin, with or without 10 μM FINDY for 8 h. The cells were then harvested and lysed in 50 mM Tris (pH 7.4), 150 mM NaCl, 0.5 mM EDTA, 1% Empigen BB and protease/phosphatase inhibitor cocktails (Nacalai Tesque). The clarified cell lysates were processed with anti-FLAG (M2) beads (Sigma-Aldrich) and the bound proteins were then eluted with glycine buffer (pH 3.0), which was immediately neutralized with 1 M Tris (pH 8.0). After reductive alkylation, the samples were trypsinized, then processed using ZipTip pipette tips containing C18 (Millipore). The digested and purified peptides were analysed by LC-MS/MS on TripleTOF 5600 (AB SCIEX). Database searches were performed using ProteinPilot Software (AB SCIEX).
RI-In vitro kinase assay
The RI-in vitro kinase assay was performed as described previously16,53, with some modifications. His-tagged human DYRK1A kinase domain (residues 127–485) was produced in E. coli then purified with Ni-NTA. GST-tagged full-length human DYRK1B recombinant proteins and His-tagged full-length human DYRK2 recombinant proteins were obtained from Life Technologies and Millipore, respectively. The kinase reaction was performed in a reaction mixture containing serially diluted inhibitors, 10 mM MOPS-KOH (pH 7.0), 10 mM magnesium acetate, 200 μM EDTA, 1 μM ATP, 0.1–0.4 μCi [γ-32P]ATP, 5 μM DYRKtide and 0.1–1 μg recombinant kinase, for a final volume of 25 μl. The final concentration of DMSO was adjusted to 1%, regardless of the inhibitor concentration. The reaction mixture was incubated at 30 °C for 10 min and phosphoric acid (final 5%) was then added to stop the reaction. We then dispensed 25 μl of the reaction mixture onto P81, a phosphocellulose membrane (Whatman, GE Healthcare), and washed four times in 5% phosphoric acid. Cherenkov light from the incorporated 32P was measured using a liquid scintillation counter. The kinase assay conditions, including the incubation period and the concentration of the kinases and substrates, were optimized to maintain linearity during the incubation. The net radioactivity was determined by subtracting the background count from the reaction mixture without kinase, and the data were expressed as a percentage of the control sample containing the solvent.
For the ATP kinetics, the same methodology was applied as above, except that the ATP concentration ranged from 1.25 to 40 μM. The amount of incorporated 32P was calculated from the standard line. The Km, Ki and Vmax values were calculated with Prism5 software (GraphPad Software) using the competitive inhibition model.
Inhibitory profiling against 275 recombinant kinases
The effects of FINDY against 275 kinases, listed in Supplementary Table 1, at an inhibitor concentration of 10 μM, were tested using the QuickScout Screening Assist Mobility Shift Assay or an immobilized metal ion affinity-based fluorescence polarization screening express kit with ATP concentration at Km or 1 mM (Carna Biosciences). Detailed information on the assay conditions is available on the website of Carna Biosciences (http://www.carnabio.com).
We selected the crystal structure of the human DYRK1A/INDY complex (RCSB Protein Data Bank accession code 3ANQ)16 as the starting model for the simulation. Docking simulations of RD0392 to DYRK1A were performed with CDOCKER and related modules in Discovery Studio 3.0 (Accelrys). As the same procedure failed to produce any reasonable binding model for FINDY, its complex with DYRK1A was built by manually modifying that for DYRK1A/RD0392 obtained above, maintaining the common moiety of the two compounds. The energy of the hypothetical DYRK1A/FINDY complex was then minimized with the same program suite.
Statistical analysis of the experimental data (Figs 6b and 7 and Supplementary Figs 7e, 9e and 10) was performed with the Mann–Whitney U-test. The data in Fig. 6d were analysed with the paired t-test. The results are shown as means±s.d. with P values (*P<0.05, **P<0.01, ***P<0.001). The data were fitted to a four-parameter logistic curve (variable slope) for Hill slope determination, from which the IC50 and EC50 values were calculated using Prism 6.0 (GraphPad Software).
How to cite this article: Kii, I. et al. Selective inhibition of the kinase DYRK1A by targeting its folding process. Nat. Commun. 7:11391 doi: 10.1038/ncomms11391 (2016).
We thank Dr Melissa Gammons (University of Bristol) and Dr Yoko Tanimura (Kyoto University) for their critical reading of the manuscript, Dr Satoshi Inouye (JNC Corporation, Yokohama, Japan) for providing the nanoKAZ gene and technical advice, Ayako Hosoya (Tokyo Medical and Dental University) for the HRMS analyses, and Kohei Araki and Dr Akiko Nakano-Kobayashi (Kyoto University) for their technical assistance. We also thank the Radioisotope Research Center of Kyoto University for instrumental support in the radioisotope experiments, and the laboratory members for their critical comments and discussion. This work was supported by Grants-in-Aid from the Japan Science and Technology Agency (J-AMP 10103930 to M.H., CREST 11103769 to M.H.), the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (KAKENHI 24241076 to M.H., Innovative Cell Biology by Innovative Technology 10102928 to M.H. and T.H.) and the Platform for Drug Discovery, Informatics, and Structural Life Science of MEXT, Japan (M.H. and T.H.).
Supplementary Figures 1-14, Supplementary Tables 1-2, Supplementary Methods and Supplementary Reference.