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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |