KinCon: Cell-based recording of full-length kinase conformations

被引:8
|
作者
Enzler, Florian [1 ,2 ]
Tschaikner, Philipp [1 ,2 ]
Schneider, Rainer [1 ,2 ]
Stefan, Eduard [1 ,2 ]
机构
[1] Univ Innsbruck, Inst Biochem, Innrain 80-82, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Ctr Mol Biosci, Innsbruck, Turkey
基金
奥地利科学基金会;
关键词
drug side effect; kinase conformations; kinase dimer; KSR; LKB1; MAPK; AMPK; MEK; molecular interaction; pseudoenzyme; pseudokinase; PKA; RAS; RAF; BRAF; CRAF; scaffolding function; STRAD alpha; undruggable; biosensor; allosteric inhibitor; oncokinase; kinase drug efficacies; PROTEIN-KINASES; CANCER; LESSONS; PLASTICITY; INHIBITORS; INSIGHTS; KINOME; LIVE;
D O I
10.1002/iub.2241
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The spectrum of kinase alterations displays distinct functional characteristics and requires kinase mutation-oriented strategies for therapeutic interference. Besides phosphotransferase activity, protein abundance, and intermolecular interactions, particular patient-mutations promote pathological kinase conformations. Despite major advances in identifying lead molecules targeting clinically relevant oncokinase functions, still many kinases are neglected and not part of drug discovery efforts. One explanation is attributed to challenges in tracking kinase activities. Chemical probes are needed to functionally annotate kinase functions, whose activities may not always depend on catalyzing phospho-transfer. Such non-catalytic kinase functions are related to transitions of full-length kinase conformations. Recent findings underline that cell-based reporter systems can be adapted to record conformation changes of kinases. Here, we discuss the possible applications of an extendable kinase conformation (KinCon) reporter toolbox for live-cell recording of kinase states. KinCon is a genetically encoded bioluminescence-based biosensor platform, which can be subjected for measurements of conformation dynamics of mutated kinases upon small molecule inhibitor exposure. We hypothesize that such biosensors can be utilized to delineate the molecular modus operandi for kinase and pseudokinase regulation. This should pave the path for full-length kinase-targeted drug discovery efforts aiming to identify single and combinatory kinase inhibitor therapies with increased specificity and efficacy.
引用
收藏
页码:1168 / 1174
页数:7
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