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Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry

[Image: see text] Biological mass spectrometry (MS) encompasses a range of methods for characterizing proteins and other biomolecules. MS is uniquely powerful for the structural analysis of endogenous protein complexes, which are often heterogeneous, poorly abundant, and refractive to characterizati...

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Detalles Bibliográficos
Autores principales: Rogawski, Rivkah, Sharon, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052418/
https://www.ncbi.nlm.nih.gov/pubmed/34406752
http://dx.doi.org/10.1021/acs.chemrev.1c00217
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author Rogawski, Rivkah
Sharon, Michal
author_facet Rogawski, Rivkah
Sharon, Michal
author_sort Rogawski, Rivkah
collection PubMed
description [Image: see text] Biological mass spectrometry (MS) encompasses a range of methods for characterizing proteins and other biomolecules. MS is uniquely powerful for the structural analysis of endogenous protein complexes, which are often heterogeneous, poorly abundant, and refractive to characterization by other methods. Here, we focus on how biological MS can contribute to the study of endogenous protein complexes, which we define as complexes expressed in the physiological host and purified intact, as opposed to reconstituted complexes assembled from heterologously expressed components. Biological MS can yield information on complex stoichiometry, heterogeneity, topology, stability, activity, modes of regulation, and even structural dynamics. We begin with a review of methods for isolating endogenous complexes. We then describe the various biological MS approaches, focusing on the type of information that each method yields. We end with future directions and challenges for these MS-based methods.
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spelling pubmed-90524182022-04-29 Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry Rogawski, Rivkah Sharon, Michal Chem Rev [Image: see text] Biological mass spectrometry (MS) encompasses a range of methods for characterizing proteins and other biomolecules. MS is uniquely powerful for the structural analysis of endogenous protein complexes, which are often heterogeneous, poorly abundant, and refractive to characterization by other methods. Here, we focus on how biological MS can contribute to the study of endogenous protein complexes, which we define as complexes expressed in the physiological host and purified intact, as opposed to reconstituted complexes assembled from heterologously expressed components. Biological MS can yield information on complex stoichiometry, heterogeneity, topology, stability, activity, modes of regulation, and even structural dynamics. We begin with a review of methods for isolating endogenous complexes. We then describe the various biological MS approaches, focusing on the type of information that each method yields. We end with future directions and challenges for these MS-based methods. American Chemical Society 2021-08-18 2022-04-27 /pmc/articles/PMC9052418/ /pubmed/34406752 http://dx.doi.org/10.1021/acs.chemrev.1c00217 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Rogawski, Rivkah
Sharon, Michal
Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry
title Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry
title_full Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry
title_fullStr Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry
title_full_unstemmed Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry
title_short Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry
title_sort characterizing endogenous protein complexes with biological mass spectrometry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052418/
https://www.ncbi.nlm.nih.gov/pubmed/34406752
http://dx.doi.org/10.1021/acs.chemrev.1c00217
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