Cargando…

Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity

[Image: see text] LIM domain kinases 1 and 2 (LIMK1 and LIMK2) regulate actin dynamics and subsequently key cellular functions such as proliferation and migration. LIMK1 and LIMK2 phosphorylate and inactivate cofilin leading to increased actin polymerization. As a result, LIMK inhibitors are emergin...

Descripción completa

Detalles Bibliográficos
Autores principales: Collins, Ross, Lee, Hyunah, Jones, D. Heulyn, Elkins, Jonathan M., Gillespie, Jason A., Thomas, Carys, Baldwin, Alex G., Jones, Kimberley, Waters, Loren, Paine, Marie, Atack, John R., Ward, Simon E., Grubisha, Olivera, Foley, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619402/
https://www.ncbi.nlm.nih.gov/pubmed/36205722
http://dx.doi.org/10.1021/acs.jmedchem.2c00751
_version_ 1784821266478268416
author Collins, Ross
Lee, Hyunah
Jones, D. Heulyn
Elkins, Jonathan M.
Gillespie, Jason A.
Thomas, Carys
Baldwin, Alex G.
Jones, Kimberley
Waters, Loren
Paine, Marie
Atack, John R.
Ward, Simon E.
Grubisha, Olivera
Foley, David W.
author_facet Collins, Ross
Lee, Hyunah
Jones, D. Heulyn
Elkins, Jonathan M.
Gillespie, Jason A.
Thomas, Carys
Baldwin, Alex G.
Jones, Kimberley
Waters, Loren
Paine, Marie
Atack, John R.
Ward, Simon E.
Grubisha, Olivera
Foley, David W.
author_sort Collins, Ross
collection PubMed
description [Image: see text] LIM domain kinases 1 and 2 (LIMK1 and LIMK2) regulate actin dynamics and subsequently key cellular functions such as proliferation and migration. LIMK1 and LIMK2 phosphorylate and inactivate cofilin leading to increased actin polymerization. As a result, LIMK inhibitors are emerging as a promising treatment strategy for certain cancers and neurological disorders. High-quality chemical probes are required if the role of these kinases in health and disease is to be understood. To that end, we report the results of a comparative assessment of 17 reported LIMK1/2 inhibitors in a variety of in vitro enzymatic and cellular assays. Our evaluation has identified three compounds (TH-257, LIJTF500025, and LIMKi3) as potent and selective inhibitors suitable for use as in vitro and in vivo pharmacological tools for the study of LIMK function in cell biology.
format Online
Article
Text
id pubmed-9619402
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-96194022022-11-01 Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity Collins, Ross Lee, Hyunah Jones, D. Heulyn Elkins, Jonathan M. Gillespie, Jason A. Thomas, Carys Baldwin, Alex G. Jones, Kimberley Waters, Loren Paine, Marie Atack, John R. Ward, Simon E. Grubisha, Olivera Foley, David W. J Med Chem [Image: see text] LIM domain kinases 1 and 2 (LIMK1 and LIMK2) regulate actin dynamics and subsequently key cellular functions such as proliferation and migration. LIMK1 and LIMK2 phosphorylate and inactivate cofilin leading to increased actin polymerization. As a result, LIMK inhibitors are emerging as a promising treatment strategy for certain cancers and neurological disorders. High-quality chemical probes are required if the role of these kinases in health and disease is to be understood. To that end, we report the results of a comparative assessment of 17 reported LIMK1/2 inhibitors in a variety of in vitro enzymatic and cellular assays. Our evaluation has identified three compounds (TH-257, LIJTF500025, and LIMKi3) as potent and selective inhibitors suitable for use as in vitro and in vivo pharmacological tools for the study of LIMK function in cell biology. American Chemical Society 2022-10-07 2022-10-27 /pmc/articles/PMC9619402/ /pubmed/36205722 http://dx.doi.org/10.1021/acs.jmedchem.2c00751 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Collins, Ross
Lee, Hyunah
Jones, D. Heulyn
Elkins, Jonathan M.
Gillespie, Jason A.
Thomas, Carys
Baldwin, Alex G.
Jones, Kimberley
Waters, Loren
Paine, Marie
Atack, John R.
Ward, Simon E.
Grubisha, Olivera
Foley, David W.
Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity
title Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity
title_full Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity
title_fullStr Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity
title_full_unstemmed Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity
title_short Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular Activity
title_sort comparative analysis of small-molecule limk1/2 inhibitors: chemical synthesis, biochemistry, and cellular activity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619402/
https://www.ncbi.nlm.nih.gov/pubmed/36205722
http://dx.doi.org/10.1021/acs.jmedchem.2c00751
work_keys_str_mv AT collinsross comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT leehyunah comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT jonesdheulyn comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT elkinsjonathanm comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT gillespiejasona comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT thomascarys comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT baldwinalexg comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT joneskimberley comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT watersloren comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT painemarie comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT atackjohnr comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT wardsimone comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT grubishaolivera comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity
AT foleydavidw comparativeanalysisofsmallmoleculelimk12inhibitorschemicalsynthesisbiochemistryandcellularactivity