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Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry
Mass spectrometry (MS) is a recognized approach for characterizing proteins and the complexes they assemble into. This application of a long-established physico-chemical tool to the frontiers of structural biology has stemmed from experiments performed in the early 1990s. While initial studies focus...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306659/ https://www.ncbi.nlm.nih.gov/pubmed/22319100 http://dx.doi.org/10.1098/rsif.2011.0823 |
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author | Hilton, Gillian R. Benesch, Justin L. P. |
author_facet | Hilton, Gillian R. Benesch, Justin L. P. |
author_sort | Hilton, Gillian R. |
collection | PubMed |
description | Mass spectrometry (MS) is a recognized approach for characterizing proteins and the complexes they assemble into. This application of a long-established physico-chemical tool to the frontiers of structural biology has stemmed from experiments performed in the early 1990s. While initial studies focused on the elucidation of stoichiometry by means of simple mass determination, developments in MS technology and methodology now allow researchers to address questions of shape, inter-subunit connectivity and protein dynamics. Here, we chart the remarkable rise of MS and its application to biomolecular complexes over the last two decades. |
format | Online Article Text |
id | pubmed-3306659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-33066592012-03-19 Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry Hilton, Gillian R. Benesch, Justin L. P. J R Soc Interface Review Articles Mass spectrometry (MS) is a recognized approach for characterizing proteins and the complexes they assemble into. This application of a long-established physico-chemical tool to the frontiers of structural biology has stemmed from experiments performed in the early 1990s. While initial studies focused on the elucidation of stoichiometry by means of simple mass determination, developments in MS technology and methodology now allow researchers to address questions of shape, inter-subunit connectivity and protein dynamics. Here, we chart the remarkable rise of MS and its application to biomolecular complexes over the last two decades. The Royal Society 2012-05-07 2012-02-08 /pmc/articles/PMC3306659/ /pubmed/22319100 http://dx.doi.org/10.1098/rsif.2011.0823 Text en This journal is © 2012 The Royal Society http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Hilton, Gillian R. Benesch, Justin L. P. Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
title | Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
title_full | Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
title_fullStr | Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
title_full_unstemmed | Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
title_short | Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
title_sort | two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306659/ https://www.ncbi.nlm.nih.gov/pubmed/22319100 http://dx.doi.org/10.1098/rsif.2011.0823 |
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