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Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin
Calmodulin (CaM) is a calcium sensor which binds and regulates a wide range of target-proteins. This implicitly enables the concentration of calcium to influence many downstream physiological responses, including muscle contraction, learning and depression. The antipsychotic drug trifluoperazine (TF...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581412/ https://www.ncbi.nlm.nih.gov/pubmed/36206305 http://dx.doi.org/10.1371/journal.pcbi.1010583 |
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author | Westerlund, Annie M. Sridhar, Akshay Dahl, Leo Andersson, Alma Bodnar, Anna-Yaroslava Delemotte, Lucie |
author_facet | Westerlund, Annie M. Sridhar, Akshay Dahl, Leo Andersson, Alma Bodnar, Anna-Yaroslava Delemotte, Lucie |
author_sort | Westerlund, Annie M. |
collection | PubMed |
description | Calmodulin (CaM) is a calcium sensor which binds and regulates a wide range of target-proteins. This implicitly enables the concentration of calcium to influence many downstream physiological responses, including muscle contraction, learning and depression. The antipsychotic drug trifluoperazine (TFP) is a known CaM inhibitor. By binding to various sites, TFP prevents CaM from associating to target-proteins. However, the molecular and state-dependent mechanisms behind CaM inhibition by drugs such as TFP are largely unknown. Here, we build a Markov state model (MSM) from adaptively sampled molecular dynamics simulations and reveal the structural and dynamical features behind the inhibitory mechanism of TFP-binding to the C-terminal domain of CaM. We specifically identify three major TFP binding-modes from the MSM macrostates, and distinguish their effect on CaM conformation by using a systematic analysis protocol based on biophysical descriptors and tools from machine learning. The results show that depending on the binding orientation, TFP effectively stabilizes features of the calcium-unbound CaM, either affecting the CaM hydrophobic binding pocket, the calcium binding sites or the secondary structure content in the bound domain. The conclusions drawn from this work may in the future serve to formulate a complete model of pharmacological modulation of CaM, which furthers our understanding of how these drugs affect signaling pathways as well as associated diseases. |
format | Online Article Text |
id | pubmed-9581412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-95814122022-10-20 Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin Westerlund, Annie M. Sridhar, Akshay Dahl, Leo Andersson, Alma Bodnar, Anna-Yaroslava Delemotte, Lucie PLoS Comput Biol Research Article Calmodulin (CaM) is a calcium sensor which binds and regulates a wide range of target-proteins. This implicitly enables the concentration of calcium to influence many downstream physiological responses, including muscle contraction, learning and depression. The antipsychotic drug trifluoperazine (TFP) is a known CaM inhibitor. By binding to various sites, TFP prevents CaM from associating to target-proteins. However, the molecular and state-dependent mechanisms behind CaM inhibition by drugs such as TFP are largely unknown. Here, we build a Markov state model (MSM) from adaptively sampled molecular dynamics simulations and reveal the structural and dynamical features behind the inhibitory mechanism of TFP-binding to the C-terminal domain of CaM. We specifically identify three major TFP binding-modes from the MSM macrostates, and distinguish their effect on CaM conformation by using a systematic analysis protocol based on biophysical descriptors and tools from machine learning. The results show that depending on the binding orientation, TFP effectively stabilizes features of the calcium-unbound CaM, either affecting the CaM hydrophobic binding pocket, the calcium binding sites or the secondary structure content in the bound domain. The conclusions drawn from this work may in the future serve to formulate a complete model of pharmacological modulation of CaM, which furthers our understanding of how these drugs affect signaling pathways as well as associated diseases. Public Library of Science 2022-10-07 /pmc/articles/PMC9581412/ /pubmed/36206305 http://dx.doi.org/10.1371/journal.pcbi.1010583 Text en © 2022 Westerlund et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Westerlund, Annie M. Sridhar, Akshay Dahl, Leo Andersson, Alma Bodnar, Anna-Yaroslava Delemotte, Lucie Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin |
title | Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin |
title_full | Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin |
title_fullStr | Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin |
title_full_unstemmed | Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin |
title_short | Markov state modelling reveals heterogeneous drug-inhibition mechanism of Calmodulin |
title_sort | markov state modelling reveals heterogeneous drug-inhibition mechanism of calmodulin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581412/ https://www.ncbi.nlm.nih.gov/pubmed/36206305 http://dx.doi.org/10.1371/journal.pcbi.1010583 |
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