Europium-conjugated pSTK (61PSTKAY), pAkt (61P15 KAYC) pMEK1/2 (61P17KAYC), cMyc (61MYCKLB) antibodies and XL665-conjugated FLAG (61FG2XLB) and His6 (61HISXLB) antibodies were purchased from Cisbio, US. Unconjugated B-Raf antibody was from Santa Cruz Biotechnology (sc-5284), pMEK1/2 antibody from Cell Signaling Technology (9121), anti-FLAG M2 from Sigma. TR-FRET assays were performed in white tissue culture 384-well or 1536-well plates (Greiner Bio One). pcDNA5TO plasmid, HEK293 T-Rex cells, hygromycin, zeocin, and blasticidin were purchased from Invitrogen. Plasmid pSEMS1-26m was obtained from Covalys. Wortmannin and LY294002 were from Calbiochem and staurosporine from Sigma. Other reference compounds were synthesized at GNF.

Peptide substrate sequences were epitope-tagged and fused to AGT, i.e. the SNAP-tag [22Keppler A, Gendreizig S, Gronemeyer T, Pick H, Vogel H, Johnsson K. A general method for the covalent labeling of fusion proteins with small molecules in vivo Nat Biotechnol 2003; 21(1): 86-9.-24Keppler A, Pick H, Arrivoli C, Vogel H, Johnsson K. Labeling of fusion proteins with synthetic fluorophores in live cells Proc Natl Acad Sci USA 2004; 101(27): 9955-.]. Generic peptide substrates sequences were previously described [17Ross H, Armstrong G, Cohen P. A non-radioactive method for the assay of many serine/threonine-specific protein kinases Biochem J 2002; 366(3): 977-81.]. For simplicity, SNAP-peptide constructs will be referred to as cSTKpep-1, 2 and 3. Complementary DNA oligonucleotides were synthesized (Valuegene) comprising the three peptide substrates with flanking Myc and FLAG epitope tags at the amino- and carboxy-terminus, respectively. Oligonucleotides were annealed and the resulting dsDNA ligated the into BamHI and NotI sites of pSEMS1-26m (Covalys). Full-length protein substrates like MEK1 were similarly epitope-tagged: A two-step PCR protocol using sense primer 5'TCAGAAGAGGATCTGATGCCCAAGAAGAAGCCGACG3' and antisense primer 5'GTCCTTGTAGTCGACGCCAGCAGCATGGGTTGG3', followed by a second PCR reaction using sense primer 5'GAACAACTCATCTCAGAAGAGGATCTGATG3', and antisense primer 5'TTACTTGTCATCGTCGTCCTTGTAGTCGAC3' to add myc (amino-terminus) and FLAG (carboxy-terminus) epitope-tags to full-length MEK1 cDNA (MGC clone ID: BC054754). The resulting second PCR product was cloned into pcDNA4 HisMax (Invitrogen). The kinase-inactive (K97M) and dominant-negative (S218/222A) constructs were generated by site-directed mutagenesis (QuikChange, Strategene) using the wild-type full-length MEK1 construct as template.

Full-length B-Raf wild-type (WT) and B-Raf(V600E) (NM_004333) cDNAs were subcloned from pcDNA3.1 into pcDNA5TO (Invitrogen) using HindIII/ Not1 restriction enzyme sites. The kinase-inactive (KD) double mutant B-Raf (V600E, K483M) was generated by site-directed mutagenesis. Akt1 (NM_005163) cDNA was subcloned from pcDNA3.1 into pcDNA5TO (Invitrogen) using BamHI/XbaI restriction enzyme sites and a C-terminal His-tag was added to the amino-terminus by PCR. The kinase-inactive AKT-KD (K179M) point mutant was generated by site-directed mutagenesis. HEK293 T-Rex cells (Invitrogen) were cultured in DMEM supplemented with 10% fetal bovine serum (Hyclone) and 5μg/ml blasticidin. Stable pools of cells constitutively expressing either cSTKpeptide or MEK1 protein substrates were generated by transfection of cDNA plasmids and selection in G418 (1 mg/ml) or zeocin (200 μg/ml), respectively. Double stable cell lines expressing tetracycline-inducible kinases were subsequently generated by transfection of these “substrate-only” HEK293 T-Rex cells and selection in medium containing 175μg/ml hygromycin B.

HEK293 cells were transfected using Fugene 6 (Roche) at a density of 8000 cells/well in 384-well plates and a final transfection volume of 30μl. The amounts of kinase and substrate plasmids per well varied for each experiment and are specified in the figure legends. Cell lysis and detection of phosphorylated or total substrate levels was performed 48h post transfection by addition of 30μl detection buffer (50 mM Hepes pH 7.2, 0.1% BSA, 20mM EDTA, 0.8M KF, and 2% Triton) containing anti-FLAG XL665 (2ng/ul) and Eu-pSTK (0.18ng/μl) or Eu-pMEK1 (0.24ng/μl). For the relative determination of total substrate levels 30μl detection buffer was added per well containing anti-FLAG XL665 (2ng/μl) and Eu-cMyc (0.3ng/μl). Plates were incubated for 3-6h at room temperature and TR-FRET readings taken on Acquest, Analyst GT (Molecular Devices Corp.), Envision or Viewlux (Perkin Elmer) plate readers. Emission readings at 671nm and 618nm were expressed as a ratio and multiplied by a constant value of 100 to obtain “TR-FRET Ratios”.

cDNA libraries and screening protocols were applied essentially as previously described [25Chanda SK, White S, Orth AP, et al. Genome-scale functional profiling of the mammalian AP-1 signaling pathway Proc Natl Acad Sci USA 2003; 100(21): 12153-8., 26Huang Q, Raya A, DeJesus P, et al. Identification of p53 regulators by genome-wide functional analysis Proc Natl Acad Sci USA 2004; 101(10): 3456-61.]. Briefly, a kinase focused library was assembled consisting of approximately 800 cDNAs encoding human or mouse derived serine/threonine and tyrosine kinases. Plasmids were arrayed into 384-well plates at 25ng per well. The transfection mixture was prepared by combining plasmid DNA for cSTKpep- 1, 2 or 3 constructs and Fugene-6, in serum-free DMEM (Invitrogen). After a 20min incubation at room temperature, 5μl of the transfection mixture was dispensed such that each well contained 3.125ng of the respective cSTKpep plasmid. Subsequently, 25μl cells were added to each well (8000/well) using μFill (Bio-Tek) dispensers. Cell lysis and plate reads were conducted 48h post transfection as described above. cDNA screens were performed in duplicates for each substrate construct. Prespotted known active kinases served as positive controls in each screen; “substrate-only” wells containing only cSTKpep plasmids served as negative controls. Kinase-induced substrate phosphorylation was expressed relative to substrate-only control wells and average fold-activation values were calculated from duplicates.

For LMW screening purposes in 384-well plates HEK293 T-Rex cells were either transiently transfected with tetracycline-inducible kinase and substrate constructs at a previously optimized ratio following the above mentioned reverse transfection protocol. Alternatively, double stable cells were plated directly at a density of 8,000cells/well in a volume of 30μl. 24h post plating, tetracycline (1μg/ml) was added to induce kinase expression for approximately 16h prior to compound addition. Kinase inhibitors were resuspended in DMSO and 12 point 1:3 serial dilutions were prepared. 100nl of compound stocks were pintool transferred into the assay plates resulting in a final DMSO concentration of 0.3%. After a 2h incubation period TR-FRET detection reagents detection reagents were added. For 1536-well plate screening cells were either transiently transfected in bulk or stable cells were seeded directly. For transient bulk transfections the transfection reagent mixture was prepared according to the following ratios: plasmid DNA: fugene 6: serum Free media = 1μg: 3μl: 21μl. For every 1ml of cells 1.25μg of kinase plasmid, 0.156μg of substrate plasmid (8:1), 4.22μl of Fugene 6 and 30μl of serum free media was prepared. The transfection mixture was then incubated at room temperature for 30 min and mixed into a HEK293 cell suspension (400 cells/μl). 2,000 cells/well were dispensed in 1536-well plates in 5μl media volumes and incubated at 37˚C. Kinase expression was induced in stable cells after 24h incubation through the addition of 1μl tetracycline (5μg/ml) followed by an additional 4-16 h incubation time before compound addition. Compound treatment in transient transfection experiments occurred 48h post seeding. In either case, 50nl DMSO stocks were pintool transferred into each well and incubated at 37˚C for a 2h period before addition of 4μl detection reagents. TR-FRET readings were taken after another incubation time of 4-24h. Z’ scores were determined as described [27Zhang JH, Chung TD, Oldenburg KR. A simple statistical parameter for use in evaluation and validation of high-throughput screening assays J Biomol Screen 1999; 4(2): 67-73.].

HEK293 cells were harvested 48h post transfection in cell lysis buffer (20 mM Tris-HCl pH 7.5, 150 mM NaCl, 1 mM Na₂EDTA, 1 mM EGTA, 1% Triton, 2.5mM sodium pyrophosphate, 1 mM Beta-glycerophosphate, 1 mM Na₃VO₄, 1ug/ml leupeptin, supplemented with 1X protease inhibitors (Sigma). Cellular extracts were resolved by SDS-PAGE (10% Bis-Tris Gel, Invitrogen), transferred to nitrocellulose membranes, and immunoblotted with the indicated antibodies. Immunolabeled proteins were visualized through Odyssey infrared imaging (Li-Cor, Lincoln, NE), with IRDye^TM800 (Rockland Immunochemicals) and AlexaFluor® 680 (Molecular Probes)-conjugated fluorescent secondary antibodies.

The B-Raf(V600E)-Ba/F3 cell line was generously provided by Markus Warmuth (GNF). Ba/F3 cells were counted and diluted to a final concentration of 75,000 cells/ml in RPMI media and 50μl/well were plated into 384-well white solid bottom plates. 50nl of a 10mM compound stock in DMSO were pintool transferred followed by a 48h incubation time at 37°C for 48h. Finally, 25μl Cell-Titer-Glo (Promega) detection reagent was added each and luminescence read were taken on a CLIPR (Molecular Devices Corp.) reader.

Cisbio’s KinEASE platform utilizes a minimal reagent set of three promiscuous peptide substrates (STK-peptides) sharing a common Ser-phosphorylation site and one corresponding phospho-specific antibody (pSTK) to support a panel of >100 biochemical Ser/Thr-kinase assays (Fig. 1A, [17Ross H, Armstrong G, Cohen P. A non-radioactive method for the assay of many serine/threonine-specific protein kinases Biochem J 2002; 366(3): 977-81.]). In vitro, the incubation of purified kinases with biotinylated peptide substrates leads to substrate phosphorylation quantifiable by TR-FRET [28Harbert C, Marshall J, Soh S, Steger K. Development of a HTRF® Kinase Assay for Determination of Syk Activity Curr Chem Gen 2008; 1: 20-6.]. We sought to translate this biochemical assay into a cellular format by first coexpressing Ser/Thr-kinases with reengineered cellular STK-peptide substrates –subsequently referred to as cSTK-pep– and then quantifying intracellular peptide phosphorylation using a simple homogeneous addition-only protocol.

Fig. (1) Schematic of biochemical and cellular TR-FRET Ser/Thr-kinase assays. (A) Biochemical KinEASE assay. (B) and (C) Cellular Ser/Thr-kinase assays. Target kinases are overexpressed in combination with cSTK peptide substrates (B) or full-length protein substrates like MEK1 (C). TR-FRET between phospho-specific and epitope-tag targeted antibodies is used to quantify intracellular substrate phosphorylation post lysis.

To this end, we flanked the STK peptide sequences with N-terminal Myc- and C-terminal Flag-epitopes. The resulting oligopeptides were fused to hAGT carrier proteins (“SNAP-tag”) [22Keppler A, Gendreizig S, Gronemeyer T, Pick H, Vogel H, Johnsson K. A general method for the covalent labeling of fusion proteins with small molecules in vivo Nat Biotechnol 2003; 21(1): 86-9.-24Keppler A, Pick H, Arrivoli C, Vogel H, Johnsson K. Labeling of fusion proteins with synthetic fluorophores in live cells Proc Natl Acad Sci USA 2004; 101(27): 9955-.] to support their stable cellular expression and to have an option for a future direct functionalization of intracellular cSTKpep-1, 2 and 3 substrates (Fig. 1B). The added epitope tags enable the quantification of either total substrate expression or substrate phosphorylation. To have a reference for peptide based cellular Ser/Thr-kinase assays we developed MEK1 as a model full-length protein substrate of kinases such as B-Raf or B-Raf(V600E), an activated oncogenic kinase mutant and established cancer drug target [31Gollob JA, Wilhelm S, Carter C, Kelley SL. Role of Raf kinase in cancer: therapeutic potential of targeting the Raf/MEK/ERK signal transduction pathway Semin Oncol 2006; 33(4): 392-406., 32Wilhelm S, Carter C, Lynch M, et al. Discovery and development of sorafenib: a multikinase inhibitor for treating cancer Nat Rev Drug Discov 2006; 5(10): 835-44.].

When the cSTKpep-3 substrate was expressed alone in HEK293 cells the observed basal phosphorylation levels derived from endogenous Ser/Thr-kinase activities were low, barely detectable by TR-FRET with weak phospho-specific bands being detectable by western blotting (Fig. 2A, C and E). Similar observations were made with peptide substrates cSTKpep-1 and cSTKpep-2 (Fig. 8 and data not shown).

Fig. (2). Case Study 1: B-Raf – Comparison of intracellular cSTKpep-3 vs. Mek1 protein substrates HEK293 cells were transiently double transfected (1µg kinase DNA and/or 1µg substrate DNA in 6-well dish) as indicated and immunoblotted. B-Raf constructs were combined with either (A) cSTKpep-3 or (B) kinase-inactive, MEK1(KD) protein substrates; (C)-(E) 384-well TR-FRET assays using a transient reverse transfection protocol. (E) B-Raf(WT) and B-Raf(V600E) constructs were cotransfected at 50ng or 25ng with a 2-fold serial dilution of cSTKpep-3 ranging from 25ng (black bar) to 1.5ng (white bar).

Fig. (8). Induction of CamK2δ activity Transient transfection reactions were performed in 384-well plates as indicated. HEK 293 were reverse transfected with 50ng CamK2δ and 50ng (black bars) or 25ng (gray bars) cSTKpep-1. CamK2δ activity was induced through 5min ionomycin treatment (1µM) and p-cSTKpep-1 was quantified by TR-FRET.

Cotransfection of cSTKpep-3 with B-Raf(V600E) resulted in a several fold increase in substrate phosphorylation by both western blotting and TR-FRET (Figs. 2A, C and E). Moreover, B-Raf(V600E)-induced cSTKpep-3 phosphorylation was both dependent on the kinase activity as well as the presence of the target phosphorylation site since no cSTKpep-3 phosphorylation was detected when using a kinase-inactive mutant version of B-Raf(V600E), B-Raf(V600E)-KD or a Ser/Ala-mutant of cSTKpep-3 (cSTK pep-3-SA) (Fig. 2A and C).

As expected, cSTKpep-3 phosphorylation could be modulated by both the amounts of substrate and kinase plasmids transfected as well as by the activation state of the transfected kinase (Fig. 2E). Comparable results were obtained when using kinase-inactive, MEK1(KD), as a substrate (Figs. 2B and D); cotransfection of MEK1 with B-Raf(V600E) resulted in increased MEK1 phosphorylation as detected by both western blotting and TR-FRET.

These results demonstrate that promiscuous Ser/Thr-kinase peptide substrates can be expressed in cells with low detectable levels of background phosphorylation and that significant increases in peptide substrate phosphorylation can be achieved through the overexpression of a target Ser/Thr-kinase. Since both the degree of background phosphorylation as well as kinase activities depend on the amounts of expression constructs applied in the transient transfection reactions, careful titrations of both constructs need to be performed to obtain optimal assay windows.

For the pharmacological evaluation we generated double stable cells constitutively expressing either cSTKpep-3, wild-type MEK1(WT) or kinase-inactive MEK1(KD) substrates in combination with Tet-inducible B-Raf(V600E). Kinase inhibitors were then tested in 384-well or 1536-well formats. In all cases short compound treatment times of around 2h were employed to minimize cytotoxicity related compound interference (Figs. 3 and 4, Table 1).

Fig. (3) Pharmacological validation of Raf(V600E)/cSTKpep-3 and Raf(V600E)/MEK(WT) TR-FRET assays. IC50 curves were determined for B-Raf inhibitor A in 384-well and 1536-well plates using double stable cell lines. Open circles: DMSO, solid squares: B-Raf inhibitor A.

Fig. (4) IC50 values of B-Raf inhibitors are strongly correlated between 384-well B-Raf(V600E) cSTKpep-3 and MEK1(WT) TR-FRET and Ba/F3 proliferation assays (Table 2). (A) TR-FRET Raf(V600E)/cSTKpep-3 vs Raf(V600E)/MEK(WT). (B) TR-FRET Raf(V600E)/cSTKpep-3 vs B-Raf(V600E)-Ba/F3. (C) TR-FRET Raf(V600E)/MEK(WT) vs B-Raf(V600E)-Ba/F3.

Table 1

IC₅₀ Profiles of B-Raf(V600E) TR-FRET and Ba/F3 Assays. Standard deviations for data are listed in parentheses (n=4-6).

Overall, cellular TR-FRET assays performed very robustly with B-Raf inhibitor A in both 384-well and 1536-well plates for MEK(WT), MEK(KD) or c-STKpep-3 substrates with Z’=0.6-0.9. Moreover, the observed potencies of a panel of selective in-house B-Raf inhibitors correlated very well in cSTKpep-3 and MEK1(WT) TR-FRET-assays (R²=0.86, Table 2, Fig. 4A). Good agreement was also observed when comparing TR-FRET assay results with historical Ba/F3-proliferation data for B-Raf(V600E) (R²_{cSTKpep-3/BaF3}=0.81, R²_MEK1/BaF3= 0.94, Table 1, Fig. 4B and 4C). None of these B-Raf inhibitors affected basal cSTKpep-3 and MEK1(WT) background phosphorylation in the absence of prior B-Raf(V600E) induction (data not shown). Finally, a selection of unrelated kinase inhibitors, including Wortmannin and LY29002 did not show any activity in either the cSTKpep-3 or MEK1(WT) TR-FRET assays (Table 1).

Table 2

An Emerging Cellular Ser/Thr-Kinase Assay Panel. Confirmed hits obtained from cSTKpep cDNA screens. fold activation was calculated as TR-FRET signal with kinase and cSTKpep cotransfection divided by cSTKpep alone.

While B-Raf selective compounds compared very well in the above assays (Table 1), pronounced discrepancies were reproducibly observed for the activities of the highly selective MEK1/2 inhibitor PD0325901 [34Solit DB, Garraway LA, Pratilas CA, et al. B-Raf mutation predicts sensitivity to MEK inhibition Nature 2006; 439(7074): 358-62., 35Smith CK, Windsor WT. Thermodynamics of nucleotide and non-ATP-competitive inhibitor binding to MEK1 by circular dichroism and isothermal titration calorimetry Biochemistry 2007; 46(5): 1358-67.] and staurosporine, a non-selective kinase inhibitor with only weak activity against Raf-kinases in vitro. Both compounds had comparable activities when using cSTKpep-3 or MEK1(WT) as B-Raf(V600E) substrates, but were inactive when using MEK1(KD). Similar observations of substrate dependent inhibitor profiles in cellular MEK-phosphorylation assays were recently made using an ELISA readout [36Ishii T, Sootome H, Yagi Y, Yamashita K, Noumi T, Noro N. A selective cellular screening assay for B-Raf and c-Raf kinases J Biomol Screen 2007; 12(6): 818-27.]. The underlying reasons for these differences are still being investigated. One possible explanation is the existence of a positive feedback loop driving ERK1/2 mediated (hyper)activation of B-Raf(V600E), although the detailed mechanism is still unclear and factors including the cellular context and predominant Raf isoforms involved may have an impact [29Balan V, Leicht DT, Zhu J, et al. Identification of novel in vivo Raf-1 phosphorylation sites mediating positive feedback Raf-1 regulation by extracellular signal-regulated kinase Mol Biol Cell 2006; 17(3): 1141-53., 30Brummer T, Naegele H, Reth M, Misawa Y. Identification of novel Erk-mediated feedback phosphorylation sites at the C-terminus of B-Raf Oncogene 2003; 22(55): 8823-34.]. According to this model, PD0325901 and staurosporine indirectly affect B-Raf(V600E) activity on cSTKpep-3 and MEK1(WT) by targeting downstream kinases and thereby antagonizing the activating feedback loop. Overexpression of MEK1(KD) on the other hand would exert the same effect as small molecule MEK1/2 inhibition, thereby rendering the residual B-Raf(V600E) activity insensitive to further PD0325901 inhibition. Regardless of the underlying mechanistic reasons for the observed discrepancies between B-Raf targeted TR-FRET assays, it is interesting to note the distinctions between the MEK1(WT) and MEK1(KD) assays. The nature and activation state of functional protein substrates can impact the cellular activities of upstream drug targets and the activity profiles of putative inhibitors. This is a potentially complicating factor that needs to be investigated when designing cellular enzyme assays around bioactive substrates [15Riddle SM, Vedvik KL, Hanson GT, Vogel KW. Time-resolved fluorescence resonance energy transfer kinase assays using physiological protein substrates: applications of terbium-fluorescein and terbium-green fluorescent protein fluorescence resonance energy transfer pairs Anal Biochem 2006; 356(1): 108-6., 16Robers MB, Horton RA, Bercher MR, Vogel KW, Machleidt T. High-throughput cellular assays for regulated posttranslational modifications Anal Biochem 2008; 372(2): 189-97.]. Biologically inactive peptide substrates on the other hand would be expected to have a comparatively minor effect on intracellular signaling pathways.

For a second case study we turned to AKT and its upstream activation pathway. AKT-dependent intracellular cSTKpep-3 phosphorylation could be detected by western blotting and by TR-FRET (Fig. 5A and 5B). In the absence of other efficacious AKT inhibitors staurosporine was used as a tool compound and found to effectively inhibit AKT-dependent cSTKpep-3 phosphorylation (Fig. 6B). Its cellular potency (IC₅₀ ~100nM) agreed with the in vitro activity against AKT (IC₅₀~100nM). Comparable IC₅₀ values were found for incubation periods ranging from 30min (IC₅₀~240nM) to 2h (IC₅₀~100nM) (data not shown).

Fig. (5). Case Study 2: AKT dependent cSTKpep-3 phosphorylation (A) HEK293 cells were transiently double transfected (1µg kinase DNA and/or 1µg substrate DNA in 6-well dish) as indicated and immunoblotted. (B) 384-well TR-FRET assay using a transient reverse transfection protocol. Wild-type Akt1(WT) or kinase-inactive Akt1(K179M) were combined with cSTKpep-3.

Fig. (6). Quantification of total- and phospho-cSTKpep levels can reveal compound interference. The importance of short compound incubation (A) Combinations of α-FLAG with α-p-STK or α-Myc antibodies were used to quantify either cSTKpep-phosphorylation or total cellular cSTKpep-3 expression by TR-FRET. (B) and (C) Transient 384-well AKT/cSTKpep-3 TR-FRET assay. Cells were treated with staurosporine for 2h (B) or 48h (C). Open circles: phospho-cSTKpep-3; Solid circles: total-cSTKpep-3.

To determine if staurosporine-induced cytotoxicity and the subsequent loss of kinase substrate expression affected the outcome of the cellular assays, we aimed to separate the effect of staurosporine on cSTKpep-3 phosphorylation from its effect on total cSTKpep-3 expression (Fig. 6A). After short 2h treatment staurosporine exclusively affected cSTKpep-3 phosphorylation, but not cSTKpep-3 expression levels. After an extended 48h treatment stauros-porine affected phospho- as well as total-cSTKpep-3 levels with equal apparent potency, suggesting that the occurrence of cytotoxicity inappropriately interfered with the assay readout.

These observations underline the importance of short compound treatment times to avoid high rates of uninteresting hits in an HTS context and further highlight the benefit of the presented cellular assay format over cell proliferation or reporter gene assays that typically require compound incubation times from several hours to days.

Next, we aimed to interrogate the AKT pathway in greater detail by separating AKT activation as indicated by Ser473 phosphorylation, from signaling events depending on activated AKT such as cSTKpep-3 phosphorylation (Fig. 7A). To this end we developed another TR-FRET assay using His-tagged AKT to monitor Ser473 phosphorylation.

Fig. (7). Targeting the AKT-pathway (A) TR-FRET assays were developed for the quantification of either p-AKT(Ser473) or p-cSTKpep-3. (B) p-AKT(Ser473) and (C) p-cSTKpep phosphorylation was quantified after treatment with Staurosporine (open triangles), Wortmannin (open squares), LY294002 (open circles) or DMSO (closed squares). Experiments were performed in 384-well plates after transient co-transfection of AKT-His and cSTKpep-3 into HEK293 cells.

As predicted for inhibitors of AKT activation, the PI3K inhibitors LY294002 and Wortmannin displayed comparable potencies in both AKT phosporylation (Fig. 7B) and cSTKpep-3 phosphorylation (Fig.7C) assays. Moreover, the observed potencies of Wortmannin and LY294002 in the low nanomolar and low micromolar concentration ranges respectively were in line with their reported in vitro and cellular activities on PI3K [37Arcaro A, Wymann MP. Wortmannin is a potent phosphatidylinositol 3–kinase inhibitor: the role of phosphatidyl-3,4,5-triphosphate in neutrophil responses Biochem J 1993; 296(2): 297-301., 38Vlahos CJ, Matter WF, Hui KY, Brown RF. A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002) J Biol Chem 1994; 269(7): 5241-8.]. Staurosporine activity on the other hand differed by a factor of ~100fold when quantifying p-AKT (IC₅₀~6μM) versus p-cSTKpep-3 (IC₅₀~60nM). These cellular activities mirror the in vitro potency of staurosporine on PI3K (IC₅₀~9μM) and AKT (IC₅₀~100nM).

Together, these experiments demonstrate that the activity of overexpressed wild-type Ser/Thr-kinases can be responsive to upstream signaling events and that assays can be designed in the proposed format to interrogate a cellular pathway at different intersection points.

Having shown proof-of-concept for two important drug targets AKT and B-Raf, we sought to identify additional Ser/Thr-kinases amenable to our cellular assay approach through cDNA screening. A kinase focused sublibrary of GNF’s genome scale cDNA collection [25Chanda SK, White S, Orth AP, et al. Genome-scale functional profiling of the mammalian AP-1 signaling pathway Proc Natl Acad Sci USA 2003; 100(21): 12153-8., 26Huang Q, Raya A, DeJesus P, et al. Identification of p53 regulators by genome-wide functional analysis Proc Natl Acad Sci USA 2004; 101(10): 3456-61.] comprising approximately 800 Ser/Thr- and Tyr-kinase clones was arrayed into microtiter plates. A panel of cSTKpep-1, 2 and 3 substrates was then screened besides a number of similarly designed SNAP-peptide constructs containing alternative substrate sequences, including Crosstide (GRPRTSSFAEPG), MBPtide (FFKKIVTPRTPPP), CREBtide (LRREIL SRRPSYRK) and the p38α-activation loop (LARHTDDEMTGYVA). cDNA hits resulting in >2fold S/N ratios relative to substrate-alone controls were picked for further activity and sequence confirmation. Between all 7 screens the three cSTKpep substrates combined scored ~86% of all hits (57/66) and overall higher S/N ratios than the other peptide substrates tested. cSTKpep-3 returned the majority of hits (37/57) followed by cSTKpep-2 (12/57) and c-Kinase-1 (8/57). Ultimately, 22 distinct Ser/Thr-kinases were identified as inducers of cSTKpep phosphorylation (Table 2). Of these 22 Ser/Thr-kinases, 13 were already known members of the biochemical KinEASE-panel, whereas 9 kinases were newly identified. Nine out of the 13 previously known kinases preferred the same STK peptide substrate in vitro and in cells (Table 2). No Tyr-kinases were found to stimulate cSTKpep phosphorylation, suggesting that no indirect Tyr-kinase induced activation of endogenous Ser/Thr-kinase pathways triggered cSTKpep phosphorylation. Overall, these observations are consistent with the idea that the intracellular kinase-cSTKpep interactions were direct.

While a number of kinases already represented on the biochemical KinEASE panel were picked up through DNA screening, others were missed. Several reasons might help explain these findings. Preactivation of Ser/Thr-kinases either through physiologic stimuli or via protein engineering, e.g. through the deletion of autoinhibitory domains or activating mutations, may be required beyond their plain overexpression to induce cSTKpep phosphorylation. The subcellular localization of kinases or their substrates, cell cycle dependency, cellular backgrounds and the dynamics of signaling pathways all may play a role. By rescreening our kinase cDNA library under modified assay conditions, e.g. in the presence of external stimuli, nuclear targeted substrates, different cell types, or alternatively through the design of an entirely new cDNA library of activated kinase constructs we aim to further expand the current panel of cellular Ser/Thr-kinase assays in the future. In the case of CamK2δ we found that transient activation of kinase activity and subsequent cSTKpep-1 phosphorylation was ionomycin inducible (Fig. 8). We believe that assay conditions can be found to activate additional Ser/Thr-kinases in a similar manner.