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Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency
Sortase mediated ligation is a highly specific platform for conjugation that relies on the specificity of the transpeptidase Sortase A (SrtA) for short peptide sequences (LPXTG and GGG). SrtA retains its specificity while accepting a wide range of potential substrates, but its broad use is limited b...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989145/ https://www.ncbi.nlm.nih.gov/pubmed/27534437 http://dx.doi.org/10.1038/srep31899 |
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author | Chen, Long Cohen, Justin Song, Xiaoda Zhao, Aishan Ye, Zi Feulner, Christine J. Doonan, Patrick Somers, Will Lin, Laura Chen, Peng R. |
author_facet | Chen, Long Cohen, Justin Song, Xiaoda Zhao, Aishan Ye, Zi Feulner, Christine J. Doonan, Patrick Somers, Will Lin, Laura Chen, Peng R. |
author_sort | Chen, Long |
collection | PubMed |
description | Sortase mediated ligation is a highly specific platform for conjugation that relies on the specificity of the transpeptidase Sortase A (SrtA) for short peptide sequences (LPXTG and GGG). SrtA retains its specificity while accepting a wide range of potential substrates, but its broad use is limited by the wild-type enzyme’s poor kinetics, which require large amounts of SrtA and extended reaction times for efficient conjugation. Prior explorations have aimed to improve the kinetics of SrtA with limited success. Herein we describe the discovery of further improved SrtA variants with increased efficiency for the conjugation reaction, and demonstrate their robustness in labelling proteins and antibodies in a site-specific manner. Our variants require significantly lower amounts of enzyme than WT SrtA and can be used to attach small molecules to the N or C-terminus of the heavy or light chain in antibodies with excellent yields. These improved variants can also be used for highly efficient site-specific PEGylation. |
format | Online Article Text |
id | pubmed-4989145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49891452016-08-30 Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency Chen, Long Cohen, Justin Song, Xiaoda Zhao, Aishan Ye, Zi Feulner, Christine J. Doonan, Patrick Somers, Will Lin, Laura Chen, Peng R. Sci Rep Article Sortase mediated ligation is a highly specific platform for conjugation that relies on the specificity of the transpeptidase Sortase A (SrtA) for short peptide sequences (LPXTG and GGG). SrtA retains its specificity while accepting a wide range of potential substrates, but its broad use is limited by the wild-type enzyme’s poor kinetics, which require large amounts of SrtA and extended reaction times for efficient conjugation. Prior explorations have aimed to improve the kinetics of SrtA with limited success. Herein we describe the discovery of further improved SrtA variants with increased efficiency for the conjugation reaction, and demonstrate their robustness in labelling proteins and antibodies in a site-specific manner. Our variants require significantly lower amounts of enzyme than WT SrtA and can be used to attach small molecules to the N or C-terminus of the heavy or light chain in antibodies with excellent yields. These improved variants can also be used for highly efficient site-specific PEGylation. Nature Publishing Group 2016-08-18 /pmc/articles/PMC4989145/ /pubmed/27534437 http://dx.doi.org/10.1038/srep31899 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Long Cohen, Justin Song, Xiaoda Zhao, Aishan Ye, Zi Feulner, Christine J. Doonan, Patrick Somers, Will Lin, Laura Chen, Peng R. Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency |
title | Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency |
title_full | Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency |
title_fullStr | Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency |
title_full_unstemmed | Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency |
title_short | Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency |
title_sort | improved variants of srta for site-specific conjugation on antibodies and proteins with high efficiency |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989145/ https://www.ncbi.nlm.nih.gov/pubmed/27534437 http://dx.doi.org/10.1038/srep31899 |
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