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Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts
The effects of spaceflight on human physiology is an increasingly studied field, yet the molecular mechanisms driving physiological changes remain unknown. With that in mind, this study was performed to obtain a deeper understanding of changes to the human proteome during space travel, by quantitati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557884/ https://www.ncbi.nlm.nih.gov/pubmed/28811532 http://dx.doi.org/10.1038/s41598-017-08432-w |
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author | Larina, Irina M. Percy, Andrew J. Yang, Juncong Borchers, Christoph H. Nosovsky, Andrei M. Grigoriev, Anatoli I. Nikolaev, Evgeny N. |
author_facet | Larina, Irina M. Percy, Andrew J. Yang, Juncong Borchers, Christoph H. Nosovsky, Andrei M. Grigoriev, Anatoli I. Nikolaev, Evgeny N. |
author_sort | Larina, Irina M. |
collection | PubMed |
description | The effects of spaceflight on human physiology is an increasingly studied field, yet the molecular mechanisms driving physiological changes remain unknown. With that in mind, this study was performed to obtain a deeper understanding of changes to the human proteome during space travel, by quantitating a panel of 125 proteins in the blood plasma of 18 Russian cosmonauts who had conducted long-duration missions to the International Space Station. The panel of labeled prototypic tryptic peptides from these proteins covered a concentration range of more than 5 orders of magnitude in human plasma. Quantitation was achieved by a well-established and highly-regarded targeted mass spectrometry approach involving multiple reaction monitoring in conjunction with stable isotope-labeled standards. Linear discriminant function analysis of the quantitative results revealed three distinct groups of proteins: 1) proteins with post-flight protein concentrations remaining stable, 2) proteins whose concentrations recovered slowly, or 3) proteins whose concentrations recovered rapidly to their pre-flight levels. Using a systems biology approach, nearly all of the reacting proteins could be linked to pathways that regulate the activities of proteases, natural immunity, lipid metabolism, coagulation cascades, or extracellular matrix metabolism. |
format | Online Article Text |
id | pubmed-5557884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55578842017-08-16 Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts Larina, Irina M. Percy, Andrew J. Yang, Juncong Borchers, Christoph H. Nosovsky, Andrei M. Grigoriev, Anatoli I. Nikolaev, Evgeny N. Sci Rep Article The effects of spaceflight on human physiology is an increasingly studied field, yet the molecular mechanisms driving physiological changes remain unknown. With that in mind, this study was performed to obtain a deeper understanding of changes to the human proteome during space travel, by quantitating a panel of 125 proteins in the blood plasma of 18 Russian cosmonauts who had conducted long-duration missions to the International Space Station. The panel of labeled prototypic tryptic peptides from these proteins covered a concentration range of more than 5 orders of magnitude in human plasma. Quantitation was achieved by a well-established and highly-regarded targeted mass spectrometry approach involving multiple reaction monitoring in conjunction with stable isotope-labeled standards. Linear discriminant function analysis of the quantitative results revealed three distinct groups of proteins: 1) proteins with post-flight protein concentrations remaining stable, 2) proteins whose concentrations recovered slowly, or 3) proteins whose concentrations recovered rapidly to their pre-flight levels. Using a systems biology approach, nearly all of the reacting proteins could be linked to pathways that regulate the activities of proteases, natural immunity, lipid metabolism, coagulation cascades, or extracellular matrix metabolism. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5557884/ /pubmed/28811532 http://dx.doi.org/10.1038/s41598-017-08432-w Text en © The Author(s) 2017 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 Larina, Irina M. Percy, Andrew J. Yang, Juncong Borchers, Christoph H. Nosovsky, Andrei M. Grigoriev, Anatoli I. Nikolaev, Evgeny N. Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts |
title | Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts |
title_full | Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts |
title_fullStr | Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts |
title_full_unstemmed | Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts |
title_short | Protein expression changes caused by spaceflight as measured for 18 Russian cosmonauts |
title_sort | protein expression changes caused by spaceflight as measured for 18 russian cosmonauts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557884/ https://www.ncbi.nlm.nih.gov/pubmed/28811532 http://dx.doi.org/10.1038/s41598-017-08432-w |
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