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A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry
Mass spectrometry is the method of choice for the characterisation of proteomes. Most proteins operate in protein complexes, in which their close association modulates their function. However, with standard MS analysis, information on protein–protein interactions is lost and no structural informatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6980279/ https://www.ncbi.nlm.nih.gov/pubmed/31593346 http://dx.doi.org/10.1002/cbic.201900611 |
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author | Stadlmeier, Michael Runtsch, Leander Simon Streshnev, Filipp Wühr, Martin Carell, Thomas |
author_facet | Stadlmeier, Michael Runtsch, Leander Simon Streshnev, Filipp Wühr, Martin Carell, Thomas |
author_sort | Stadlmeier, Michael |
collection | PubMed |
description | Mass spectrometry is the method of choice for the characterisation of proteomes. Most proteins operate in protein complexes, in which their close association modulates their function. However, with standard MS analysis, information on protein–protein interactions is lost and no structural information is retained. To gain structural and interactome data, new crosslinking reagents are needed that freeze inter‐ and intramolecular interactions. Herein, the development of a new reagent, which has several features that enable highly sensitive crosslinking MS, is reported. The reagent enables enrichment of crosslinked peptides from the majority of background peptides to facilitate efficient detection of low‐abundant crosslinked peptides. Due to the special cleavable properties, the reagent can be used for MS(2) and potentially for MS(3) experiments. Thus, the new crosslinking reagent, in combination with high‐end MS, should enable sensitive analysis of interactomes, which will help researchers to obtain important insights into cellular states in health and diseases. |
format | Online Article Text |
id | pubmed-6980279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69802792020-02-11 A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry Stadlmeier, Michael Runtsch, Leander Simon Streshnev, Filipp Wühr, Martin Carell, Thomas Chembiochem Communications Mass spectrometry is the method of choice for the characterisation of proteomes. Most proteins operate in protein complexes, in which their close association modulates their function. However, with standard MS analysis, information on protein–protein interactions is lost and no structural information is retained. To gain structural and interactome data, new crosslinking reagents are needed that freeze inter‐ and intramolecular interactions. Herein, the development of a new reagent, which has several features that enable highly sensitive crosslinking MS, is reported. The reagent enables enrichment of crosslinked peptides from the majority of background peptides to facilitate efficient detection of low‐abundant crosslinked peptides. Due to the special cleavable properties, the reagent can be used for MS(2) and potentially for MS(3) experiments. Thus, the new crosslinking reagent, in combination with high‐end MS, should enable sensitive analysis of interactomes, which will help researchers to obtain important insights into cellular states in health and diseases. John Wiley and Sons Inc. 2019-11-28 2020-01-15 /pmc/articles/PMC6980279/ /pubmed/31593346 http://dx.doi.org/10.1002/cbic.201900611 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Stadlmeier, Michael Runtsch, Leander Simon Streshnev, Filipp Wühr, Martin Carell, Thomas A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry |
title | A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry |
title_full | A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry |
title_fullStr | A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry |
title_full_unstemmed | A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry |
title_short | A Click‐Chemistry‐Based Enrichable Crosslinker for Structural and Protein Interaction Analysis by Mass Spectrometry |
title_sort | click‐chemistry‐based enrichable crosslinker for structural and protein interaction analysis by mass spectrometry |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6980279/ https://www.ncbi.nlm.nih.gov/pubmed/31593346 http://dx.doi.org/10.1002/cbic.201900611 |
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