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The diverse and expanding role of mass spectrometry in structural and molecular biology

The emergence of proteomics has led to major technological advances in mass spectrometry (MS). These advancements not only benefitted MS‐based high‐throughput proteomics but also increased the impact of mass spectrometry on the field of structural and molecular biology. Here, we review how state‐of‐...

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Autores principales: Lössl, Philip, van de Waterbeemd, Michiel, Heck, Albert JR
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167345/
https://www.ncbi.nlm.nih.gov/pubmed/27797822
http://dx.doi.org/10.15252/embj.201694818
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author Lössl, Philip
van de Waterbeemd, Michiel
Heck, Albert JR
author_facet Lössl, Philip
van de Waterbeemd, Michiel
Heck, Albert JR
author_sort Lössl, Philip
collection PubMed
description The emergence of proteomics has led to major technological advances in mass spectrometry (MS). These advancements not only benefitted MS‐based high‐throughput proteomics but also increased the impact of mass spectrometry on the field of structural and molecular biology. Here, we review how state‐of‐the‐art MS methods, including native MS, top‐down protein sequencing, cross‐linking‐MS, and hydrogen–deuterium exchange‐MS, nowadays enable the characterization of biomolecular structures, functions, and interactions. In particular, we focus on the role of mass spectrometry in integrated structural and molecular biology investigations of biological macromolecular complexes and cellular machineries, highlighting work on CRISPR–Cas systems and eukaryotic transcription complexes.
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spelling pubmed-51673452016-12-28 The diverse and expanding role of mass spectrometry in structural and molecular biology Lössl, Philip van de Waterbeemd, Michiel Heck, Albert JR EMBO J Review The emergence of proteomics has led to major technological advances in mass spectrometry (MS). These advancements not only benefitted MS‐based high‐throughput proteomics but also increased the impact of mass spectrometry on the field of structural and molecular biology. Here, we review how state‐of‐the‐art MS methods, including native MS, top‐down protein sequencing, cross‐linking‐MS, and hydrogen–deuterium exchange‐MS, nowadays enable the characterization of biomolecular structures, functions, and interactions. In particular, we focus on the role of mass spectrometry in integrated structural and molecular biology investigations of biological macromolecular complexes and cellular machineries, highlighting work on CRISPR–Cas systems and eukaryotic transcription complexes. John Wiley and Sons Inc. 2016-10-26 2016-12-15 /pmc/articles/PMC5167345/ /pubmed/27797822 http://dx.doi.org/10.15252/embj.201694818 Text en © 2016 The Authors. Published under the terms of the CC BY NC ND 4.0 license This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Lössl, Philip
van de Waterbeemd, Michiel
Heck, Albert JR
The diverse and expanding role of mass spectrometry in structural and molecular biology
title The diverse and expanding role of mass spectrometry in structural and molecular biology
title_full The diverse and expanding role of mass spectrometry in structural and molecular biology
title_fullStr The diverse and expanding role of mass spectrometry in structural and molecular biology
title_full_unstemmed The diverse and expanding role of mass spectrometry in structural and molecular biology
title_short The diverse and expanding role of mass spectrometry in structural and molecular biology
title_sort diverse and expanding role of mass spectrometry in structural and molecular biology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167345/
https://www.ncbi.nlm.nih.gov/pubmed/27797822
http://dx.doi.org/10.15252/embj.201694818
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