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Selectivity and stability of N-terminal targeting protein modification chemistries
Protein N-termini provide uniquely reactive motifs for single site protein modification. Though a number of reactions have been developed to target this site, the selectivity, generality, and stability of the conjugates formed has not been studied. We have therefore undertaken a comprehensive compar...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811658/ https://www.ncbi.nlm.nih.gov/pubmed/36685256 http://dx.doi.org/10.1039/d2cb00203e |
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author | Barber, Lydia J. Yates, Nicholas D. J. Fascione, Martin A. Parkin, Alison Hemsworth, Glyn R. Genever, Paul G. Spicer, Christopher D. |
author_facet | Barber, Lydia J. Yates, Nicholas D. J. Fascione, Martin A. Parkin, Alison Hemsworth, Glyn R. Genever, Paul G. Spicer, Christopher D. |
author_sort | Barber, Lydia J. |
collection | PubMed |
description | Protein N-termini provide uniquely reactive motifs for single site protein modification. Though a number of reactions have been developed to target this site, the selectivity, generality, and stability of the conjugates formed has not been studied. We have therefore undertaken a comprehensive comparative study of the most promising methods for N-terminal protein modification, and find that there is no ‘one size fits all’ approach, necessitating reagent screening for a particular protein or application. Moreover, we observed limited stability in all cases, leading to a need for continued innovation and development in the bioconjugation field. |
format | Online Article Text |
id | pubmed-9811658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-98116582023-01-20 Selectivity and stability of N-terminal targeting protein modification chemistries Barber, Lydia J. Yates, Nicholas D. J. Fascione, Martin A. Parkin, Alison Hemsworth, Glyn R. Genever, Paul G. Spicer, Christopher D. RSC Chem Biol Chemistry Protein N-termini provide uniquely reactive motifs for single site protein modification. Though a number of reactions have been developed to target this site, the selectivity, generality, and stability of the conjugates formed has not been studied. We have therefore undertaken a comprehensive comparative study of the most promising methods for N-terminal protein modification, and find that there is no ‘one size fits all’ approach, necessitating reagent screening for a particular protein or application. Moreover, we observed limited stability in all cases, leading to a need for continued innovation and development in the bioconjugation field. RSC 2022-11-17 /pmc/articles/PMC9811658/ /pubmed/36685256 http://dx.doi.org/10.1039/d2cb00203e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Barber, Lydia J. Yates, Nicholas D. J. Fascione, Martin A. Parkin, Alison Hemsworth, Glyn R. Genever, Paul G. Spicer, Christopher D. Selectivity and stability of N-terminal targeting protein modification chemistries |
title | Selectivity and stability of N-terminal targeting protein modification chemistries |
title_full | Selectivity and stability of N-terminal targeting protein modification chemistries |
title_fullStr | Selectivity and stability of N-terminal targeting protein modification chemistries |
title_full_unstemmed | Selectivity and stability of N-terminal targeting protein modification chemistries |
title_short | Selectivity and stability of N-terminal targeting protein modification chemistries |
title_sort | selectivity and stability of n-terminal targeting protein modification chemistries |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811658/ https://www.ncbi.nlm.nih.gov/pubmed/36685256 http://dx.doi.org/10.1039/d2cb00203e |
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