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High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers
BACKGROUND: Skeletal muscles are composed of a heterogeneous collection of fiber types with different physiological adaption in response to a stimulus and disease-related conditions. Each fiber has a specific molecular expression of myosin heavy chain molecules (MyHC). So far, MyHCs are currently th...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087369/ https://www.ncbi.nlm.nih.gov/pubmed/32293536 http://dx.doi.org/10.1186/s13395-020-00226-5 |
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author | Kallabis, Sebastian Abraham, Lena Müller, Stefan Dzialas, Verena Türk, Clara Wiederstein, Janica Lea Bock, Theresa Nolte, Hendrik Nogara, Leonardo Blaauw, Bert Braun, Thomas Krüger, Marcus |
author_facet | Kallabis, Sebastian Abraham, Lena Müller, Stefan Dzialas, Verena Türk, Clara Wiederstein, Janica Lea Bock, Theresa Nolte, Hendrik Nogara, Leonardo Blaauw, Bert Braun, Thomas Krüger, Marcus |
author_sort | Kallabis, Sebastian |
collection | PubMed |
description | BACKGROUND: Skeletal muscles are composed of a heterogeneous collection of fiber types with different physiological adaption in response to a stimulus and disease-related conditions. Each fiber has a specific molecular expression of myosin heavy chain molecules (MyHC). So far, MyHCs are currently the best marker proteins for characterization of individual fiber types, and several proteome profiling studies have helped to dissect the molecular signature of whole muscles and individual fibers. METHODS: Herein, we describe a mass spectrometric workflow to measure skeletal muscle fiber type-specific proteomes. To bypass the limited quantities of protein in single fibers, we developed a Proteomics high-throughput fiber typing (ProFiT) approach enabling profiling of MyHC in single fibers. Aliquots of protein extracts from separated muscle fibers were subjected to capillary LC-MS gradients to profile MyHC isoforms in a 96-well format. Muscle fibers with the same MyHC protein expression were pooled and subjected to proteomic, pulsed-SILAC, and phosphoproteomic analysis. RESULTS: Our fiber type-specific quantitative proteome analysis confirmed the distribution of fiber types in the soleus muscle, substantiates metabolic adaptions in oxidative and glycolytic fibers, and highlighted significant differences between the proteomes of type IIb fibers from different muscle groups, including a differential expression of desmin and actinin-3. A detailed map of the Lys-6 incorporation rates in muscle fibers showed an increased turnover of slow fibers compared to fast fibers. In addition, labeling of mitochondrial respiratory chain complexes revealed a broad range of Lys-6 incorporation rates, depending on the localization of the subunits within distinct complexes. CONCLUSION: Overall, the ProFiT approach provides a versatile tool to rapidly characterize muscle fibers and obtain fiber-specific proteomes for different muscle groups. |
format | Online Article Text |
id | pubmed-7087369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70873692020-03-24 High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers Kallabis, Sebastian Abraham, Lena Müller, Stefan Dzialas, Verena Türk, Clara Wiederstein, Janica Lea Bock, Theresa Nolte, Hendrik Nogara, Leonardo Blaauw, Bert Braun, Thomas Krüger, Marcus Skelet Muscle Methodology BACKGROUND: Skeletal muscles are composed of a heterogeneous collection of fiber types with different physiological adaption in response to a stimulus and disease-related conditions. Each fiber has a specific molecular expression of myosin heavy chain molecules (MyHC). So far, MyHCs are currently the best marker proteins for characterization of individual fiber types, and several proteome profiling studies have helped to dissect the molecular signature of whole muscles and individual fibers. METHODS: Herein, we describe a mass spectrometric workflow to measure skeletal muscle fiber type-specific proteomes. To bypass the limited quantities of protein in single fibers, we developed a Proteomics high-throughput fiber typing (ProFiT) approach enabling profiling of MyHC in single fibers. Aliquots of protein extracts from separated muscle fibers were subjected to capillary LC-MS gradients to profile MyHC isoforms in a 96-well format. Muscle fibers with the same MyHC protein expression were pooled and subjected to proteomic, pulsed-SILAC, and phosphoproteomic analysis. RESULTS: Our fiber type-specific quantitative proteome analysis confirmed the distribution of fiber types in the soleus muscle, substantiates metabolic adaptions in oxidative and glycolytic fibers, and highlighted significant differences between the proteomes of type IIb fibers from different muscle groups, including a differential expression of desmin and actinin-3. A detailed map of the Lys-6 incorporation rates in muscle fibers showed an increased turnover of slow fibers compared to fast fibers. In addition, labeling of mitochondrial respiratory chain complexes revealed a broad range of Lys-6 incorporation rates, depending on the localization of the subunits within distinct complexes. CONCLUSION: Overall, the ProFiT approach provides a versatile tool to rapidly characterize muscle fibers and obtain fiber-specific proteomes for different muscle groups. BioMed Central 2020-03-23 /pmc/articles/PMC7087369/ /pubmed/32293536 http://dx.doi.org/10.1186/s13395-020-00226-5 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Kallabis, Sebastian Abraham, Lena Müller, Stefan Dzialas, Verena Türk, Clara Wiederstein, Janica Lea Bock, Theresa Nolte, Hendrik Nogara, Leonardo Blaauw, Bert Braun, Thomas Krüger, Marcus High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers |
title | High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers |
title_full | High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers |
title_fullStr | High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers |
title_full_unstemmed | High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers |
title_short | High-throughput proteomics fiber typing (ProFiT) for comprehensive characterization of single skeletal muscle fibers |
title_sort | high-throughput proteomics fiber typing (profit) for comprehensive characterization of single skeletal muscle fibers |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087369/ https://www.ncbi.nlm.nih.gov/pubmed/32293536 http://dx.doi.org/10.1186/s13395-020-00226-5 |
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