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

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 ki...

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Autores principales: Enzler, Florian, Tschaikner, Philipp, Schneider, Rainer, Stefan, Eduard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318358/
https://www.ncbi.nlm.nih.gov/pubmed/32027084
http://dx.doi.org/10.1002/iub.2241
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author Enzler, Florian
Tschaikner, Philipp
Schneider, Rainer
Stefan, Eduard
author_facet Enzler, Florian
Tschaikner, Philipp
Schneider, Rainer
Stefan, Eduard
author_sort Enzler, Florian
collection PubMed
description 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.
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spelling pubmed-73183582020-06-29 KinCon: Cell‐based recording of full‐length kinase conformations Enzler, Florian Tschaikner, Philipp Schneider, Rainer Stefan, Eduard IUBMB Life Hypothesis 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. John Wiley & Sons, Inc. 2020-02-06 2020-06 /pmc/articles/PMC7318358/ /pubmed/32027084 http://dx.doi.org/10.1002/iub.2241 Text en © 2020 The Authors. IUBMB Life published by Wiley Periodicals, Inc. on behalf of International Union of Biochemistry and Molecular Biology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hypothesis
Enzler, Florian
Tschaikner, Philipp
Schneider, Rainer
Stefan, Eduard
KinCon: Cell‐based recording of full‐length kinase conformations
title KinCon: Cell‐based recording of full‐length kinase conformations
title_full KinCon: Cell‐based recording of full‐length kinase conformations
title_fullStr KinCon: Cell‐based recording of full‐length kinase conformations
title_full_unstemmed KinCon: Cell‐based recording of full‐length kinase conformations
title_short KinCon: Cell‐based recording of full‐length kinase conformations
title_sort kincon: cell‐based recording of full‐length kinase conformations
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318358/
https://www.ncbi.nlm.nih.gov/pubmed/32027084
http://dx.doi.org/10.1002/iub.2241
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