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Large Scale Chemical Cross-linking Mass Spectrometry Perspectives

The spectacular heterogeneity of a complex protein mixture from biological samples becomes even more difficult to tackle when one’s attention is shifted towards different protein complex topologies, transient interactions, or localization of PPIs. Meticulous protein-by-protein affinity pull-downs an...

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Autores principales: Zybailov, Boris L., Glazko, Galina V., Jaiswal, Mihir, Raney, Kevin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101816/
https://www.ncbi.nlm.nih.gov/pubmed/25045217
http://dx.doi.org/10.4172/jpb.S2-001
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author Zybailov, Boris L.
Glazko, Galina V.
Jaiswal, Mihir
Raney, Kevin D.
author_facet Zybailov, Boris L.
Glazko, Galina V.
Jaiswal, Mihir
Raney, Kevin D.
author_sort Zybailov, Boris L.
collection PubMed
description The spectacular heterogeneity of a complex protein mixture from biological samples becomes even more difficult to tackle when one’s attention is shifted towards different protein complex topologies, transient interactions, or localization of PPIs. Meticulous protein-by-protein affinity pull-downs and yeast-two-hybrid screens are the two approaches currently used to decipher proteome-wide interaction networks. Another method is to employ chemical cross-linking, which gives not only identities of interactors, but could also provide information on the sites of interactions and interaction interfaces. Despite significant advances in mass spectrometry instrumentation over the last decade, mapping Protein-Protein Interactions (PPIs) using chemical cross-linking remains time consuming and requires substantial expertise, even in the simplest of systems. While robust methodologies and software exist for the analysis of binary PPIs and also for the single protein structure refinement using cross-linking-derived constraints, undertaking a proteome-wide cross-linking study is highly complex. Difficulties include i) identifying cross-linkers of the right length and selectivity that could capture interactions of interest; ii) enrichment of the cross-linked species; iii) identification and validation of the cross-linked peptides and cross-linked sites. In this review we examine existing literature aimed at the large-scale protein cross-linking and discuss possible paths for improvement. We also discuss short-length cross-linkers of broad specificity such as formaldehyde and diazirine-based photo-cross-linkers. These cross-linkers could potentially capture many types of interactions, without strict requirement for a particular amino-acid to be present at a given protein-protein interface. How these shortlength, broad specificity cross-linkers be applied to proteome-wide studies? We will suggest specific advances in methodology, instrumentation and software that are needed to make such a leap.
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spelling pubmed-41018162014-07-17 Large Scale Chemical Cross-linking Mass Spectrometry Perspectives Zybailov, Boris L. Glazko, Galina V. Jaiswal, Mihir Raney, Kevin D. J Proteomics Bioinform Article The spectacular heterogeneity of a complex protein mixture from biological samples becomes even more difficult to tackle when one’s attention is shifted towards different protein complex topologies, transient interactions, or localization of PPIs. Meticulous protein-by-protein affinity pull-downs and yeast-two-hybrid screens are the two approaches currently used to decipher proteome-wide interaction networks. Another method is to employ chemical cross-linking, which gives not only identities of interactors, but could also provide information on the sites of interactions and interaction interfaces. Despite significant advances in mass spectrometry instrumentation over the last decade, mapping Protein-Protein Interactions (PPIs) using chemical cross-linking remains time consuming and requires substantial expertise, even in the simplest of systems. While robust methodologies and software exist for the analysis of binary PPIs and also for the single protein structure refinement using cross-linking-derived constraints, undertaking a proteome-wide cross-linking study is highly complex. Difficulties include i) identifying cross-linkers of the right length and selectivity that could capture interactions of interest; ii) enrichment of the cross-linked species; iii) identification and validation of the cross-linked peptides and cross-linked sites. In this review we examine existing literature aimed at the large-scale protein cross-linking and discuss possible paths for improvement. We also discuss short-length cross-linkers of broad specificity such as formaldehyde and diazirine-based photo-cross-linkers. These cross-linkers could potentially capture many types of interactions, without strict requirement for a particular amino-acid to be present at a given protein-protein interface. How these shortlength, broad specificity cross-linkers be applied to proteome-wide studies? We will suggest specific advances in methodology, instrumentation and software that are needed to make such a leap. 2013-02-08 /pmc/articles/PMC4101816/ /pubmed/25045217 http://dx.doi.org/10.4172/jpb.S2-001 Text en © 2013 Zybailov BL, et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Zybailov, Boris L.
Glazko, Galina V.
Jaiswal, Mihir
Raney, Kevin D.
Large Scale Chemical Cross-linking Mass Spectrometry Perspectives
title Large Scale Chemical Cross-linking Mass Spectrometry Perspectives
title_full Large Scale Chemical Cross-linking Mass Spectrometry Perspectives
title_fullStr Large Scale Chemical Cross-linking Mass Spectrometry Perspectives
title_full_unstemmed Large Scale Chemical Cross-linking Mass Spectrometry Perspectives
title_short Large Scale Chemical Cross-linking Mass Spectrometry Perspectives
title_sort large scale chemical cross-linking mass spectrometry perspectives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101816/
https://www.ncbi.nlm.nih.gov/pubmed/25045217
http://dx.doi.org/10.4172/jpb.S2-001
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