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A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres
Many skeletal muscle proteins are present in a cell-specific or fibre-type dependent manner. Stimuli such as exercise, aging, and disease have been reported to result in fibre-specific responses in protein abundances. Thus, fibre-type-specific determination of the content of specific proteins provid...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482153/ https://www.ncbi.nlm.nih.gov/pubmed/31019216 http://dx.doi.org/10.1038/s41598-019-42168-z |
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author | Christiansen, Danny MacInnis, Martin J. Zacharewicz, Evelyn Xu, Hongyang Frankish, Barnaby P. Murphy, Robyn M. |
author_facet | Christiansen, Danny MacInnis, Martin J. Zacharewicz, Evelyn Xu, Hongyang Frankish, Barnaby P. Murphy, Robyn M. |
author_sort | Christiansen, Danny |
collection | PubMed |
description | Many skeletal muscle proteins are present in a cell-specific or fibre-type dependent manner. Stimuli such as exercise, aging, and disease have been reported to result in fibre-specific responses in protein abundances. Thus, fibre-type-specific determination of the content of specific proteins provides enhanced mechanistic understanding of muscle physiology and biochemistry compared with typically performed whole-muscle homogenate analyses. This analysis, however, is laborious and typically not performed. We present a novel dot blotting method for easy and rapid determination of skeletal muscle fibre type based on myosin heavy chain (MHC) isoform presence. Requiring only small amounts of starting muscle tissue (i.e., 2–10 mg wet weight), muscle fibre type is determined in one-tenth of a 1–3-mm fibre segment, with the remainder of each segment pooled with fibre segments of the same type (I or II) for subsequent protein quantification by western blotting. This method, which we validated using standard western blotting, is much simpler and cheaper than previous methods and is adaptable for laboratories routinely performing biochemical analyses. Use of dot blotting for fibre typing will facilitate investigations of fibre-specific responses to diverse stimuli, which will advance our understanding of skeletal muscle physiology and biochemistry. |
format | Online Article Text |
id | pubmed-6482153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64821532019-05-03 A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres Christiansen, Danny MacInnis, Martin J. Zacharewicz, Evelyn Xu, Hongyang Frankish, Barnaby P. Murphy, Robyn M. Sci Rep Article Many skeletal muscle proteins are present in a cell-specific or fibre-type dependent manner. Stimuli such as exercise, aging, and disease have been reported to result in fibre-specific responses in protein abundances. Thus, fibre-type-specific determination of the content of specific proteins provides enhanced mechanistic understanding of muscle physiology and biochemistry compared with typically performed whole-muscle homogenate analyses. This analysis, however, is laborious and typically not performed. We present a novel dot blotting method for easy and rapid determination of skeletal muscle fibre type based on myosin heavy chain (MHC) isoform presence. Requiring only small amounts of starting muscle tissue (i.e., 2–10 mg wet weight), muscle fibre type is determined in one-tenth of a 1–3-mm fibre segment, with the remainder of each segment pooled with fibre segments of the same type (I or II) for subsequent protein quantification by western blotting. This method, which we validated using standard western blotting, is much simpler and cheaper than previous methods and is adaptable for laboratories routinely performing biochemical analyses. Use of dot blotting for fibre typing will facilitate investigations of fibre-specific responses to diverse stimuli, which will advance our understanding of skeletal muscle physiology and biochemistry. Nature Publishing Group UK 2019-04-24 /pmc/articles/PMC6482153/ /pubmed/31019216 http://dx.doi.org/10.1038/s41598-019-42168-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Christiansen, Danny MacInnis, Martin J. Zacharewicz, Evelyn Xu, Hongyang Frankish, Barnaby P. Murphy, Robyn M. A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
title | A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
title_full | A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
title_fullStr | A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
title_full_unstemmed | A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
title_short | A fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
title_sort | fast, reliable and sample-sparing method to identify fibre types of single muscle fibres |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482153/ https://www.ncbi.nlm.nih.gov/pubmed/31019216 http://dx.doi.org/10.1038/s41598-019-42168-z |
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