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Design and synthesis of cysteine-specific labels for photo-crosslinking studies

Chemical cross-linking mass-spectrometry (XL-MS) represents a powerful methodology to map ligand/biomacromolecule interactions, particularly where conventional methods such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy or cryo-electron microscopy (EM) are not feasible. In t...

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Detalles Bibliográficos
Autores principales: Walko, Martin, Hewitt, Eric, Radford, Sheena E., Wilson, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061181/
https://www.ncbi.nlm.nih.gov/pubmed/35521201
http://dx.doi.org/10.1039/c8ra10436k
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author Walko, Martin
Hewitt, Eric
Radford, Sheena E.
Wilson, Andrew J.
author_facet Walko, Martin
Hewitt, Eric
Radford, Sheena E.
Wilson, Andrew J.
author_sort Walko, Martin
collection PubMed
description Chemical cross-linking mass-spectrometry (XL-MS) represents a powerful methodology to map ligand/biomacromolecule interactions, particularly where conventional methods such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy or cryo-electron microscopy (EM) are not feasible. In this manuscript, we describe the design and synthesis of two new photo-crosslinking reagents that can be used to specifically label free thiols through either maleimido or methanethiosulfonate groups and facilitate PXL-MS workflows. Both crosslinkers are based on light sensitive diazirines – precursors of highly reactive carbenes which offer additional advantages over alternative crosslinking groups such as benzophenones and aryl nitrenes given the controlled rapid and more indiscriminate reactivity.
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spelling pubmed-90611812022-05-04 Design and synthesis of cysteine-specific labels for photo-crosslinking studies Walko, Martin Hewitt, Eric Radford, Sheena E. Wilson, Andrew J. RSC Adv Chemistry Chemical cross-linking mass-spectrometry (XL-MS) represents a powerful methodology to map ligand/biomacromolecule interactions, particularly where conventional methods such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy or cryo-electron microscopy (EM) are not feasible. In this manuscript, we describe the design and synthesis of two new photo-crosslinking reagents that can be used to specifically label free thiols through either maleimido or methanethiosulfonate groups and facilitate PXL-MS workflows. Both crosslinkers are based on light sensitive diazirines – precursors of highly reactive carbenes which offer additional advantages over alternative crosslinking groups such as benzophenones and aryl nitrenes given the controlled rapid and more indiscriminate reactivity. The Royal Society of Chemistry 2019-03-07 /pmc/articles/PMC9061181/ /pubmed/35521201 http://dx.doi.org/10.1039/c8ra10436k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Walko, Martin
Hewitt, Eric
Radford, Sheena E.
Wilson, Andrew J.
Design and synthesis of cysteine-specific labels for photo-crosslinking studies
title Design and synthesis of cysteine-specific labels for photo-crosslinking studies
title_full Design and synthesis of cysteine-specific labels for photo-crosslinking studies
title_fullStr Design and synthesis of cysteine-specific labels for photo-crosslinking studies
title_full_unstemmed Design and synthesis of cysteine-specific labels for photo-crosslinking studies
title_short Design and synthesis of cysteine-specific labels for photo-crosslinking studies
title_sort design and synthesis of cysteine-specific labels for photo-crosslinking studies
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061181/
https://www.ncbi.nlm.nih.gov/pubmed/35521201
http://dx.doi.org/10.1039/c8ra10436k
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