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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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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. |
format | Online Article Text |
id | pubmed-9061181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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