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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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Autores principales: Hilton, Gillian R., Benesch, Justin L. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2012
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.
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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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