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Conformation-regulated mechanosensory control via titin domains in cardiac muscle
The giant filamentous protein titin is ideally positioned in the muscle sarcomere to sense mechanical stimuli and transform them into biochemical signals, such as those triggering cardiac hypertrophy. In this review, we ponder the evidence for signaling hotspots along the titin filament involved in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114084/ https://www.ncbi.nlm.nih.gov/pubmed/21347754 http://dx.doi.org/10.1007/s00424-011-0938-1 |
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author | Voelkel, Tobias Linke, Wolfgang A. |
author_facet | Voelkel, Tobias Linke, Wolfgang A. |
author_sort | Voelkel, Tobias |
collection | PubMed |
description | The giant filamentous protein titin is ideally positioned in the muscle sarcomere to sense mechanical stimuli and transform them into biochemical signals, such as those triggering cardiac hypertrophy. In this review, we ponder the evidence for signaling hotspots along the titin filament involved in mechanosensory control mechanisms. On the way, we distinguish between stress and strain as triggers of mechanical signaling events at the cardiac sarcomere. Whereas the Z-disk and M-band regions of titin may be prominently involved in sensing mechanical stress, signaling hotspots within the elastic I-band titin segment may respond primarily to mechanical strain. Common to both stress and strain sensor elements is their regulation by conformational changes in protein domains. |
format | Online Article Text |
id | pubmed-3114084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-31140842011-07-14 Conformation-regulated mechanosensory control via titin domains in cardiac muscle Voelkel, Tobias Linke, Wolfgang A. Pflugers Arch Invited Review The giant filamentous protein titin is ideally positioned in the muscle sarcomere to sense mechanical stimuli and transform them into biochemical signals, such as those triggering cardiac hypertrophy. In this review, we ponder the evidence for signaling hotspots along the titin filament involved in mechanosensory control mechanisms. On the way, we distinguish between stress and strain as triggers of mechanical signaling events at the cardiac sarcomere. Whereas the Z-disk and M-band regions of titin may be prominently involved in sensing mechanical stress, signaling hotspots within the elastic I-band titin segment may respond primarily to mechanical strain. Common to both stress and strain sensor elements is their regulation by conformational changes in protein domains. Springer-Verlag 2011-02-25 2011 /pmc/articles/PMC3114084/ /pubmed/21347754 http://dx.doi.org/10.1007/s00424-011-0938-1 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Invited Review Voelkel, Tobias Linke, Wolfgang A. Conformation-regulated mechanosensory control via titin domains in cardiac muscle |
title | Conformation-regulated mechanosensory control via titin domains in cardiac muscle |
title_full | Conformation-regulated mechanosensory control via titin domains in cardiac muscle |
title_fullStr | Conformation-regulated mechanosensory control via titin domains in cardiac muscle |
title_full_unstemmed | Conformation-regulated mechanosensory control via titin domains in cardiac muscle |
title_short | Conformation-regulated mechanosensory control via titin domains in cardiac muscle |
title_sort | conformation-regulated mechanosensory control via titin domains in cardiac muscle |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114084/ https://www.ncbi.nlm.nih.gov/pubmed/21347754 http://dx.doi.org/10.1007/s00424-011-0938-1 |
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