Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783550830315569152 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7318358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT enzlerflorian kinconcellbasedrecordingoffulllengthkinaseconformations AT tschaiknerphilipp kinconcellbasedrecordingoffulllengthkinaseconformations AT schneiderrainer kinconcellbasedrecordingoffulllengthkinaseconformations AT stefaneduard kinconcellbasedrecordingoffulllengthkinaseconformations |