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Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption
Genetically encoded covalent peptide tagging technology, such as the SpyTag–SpyCatcher reaction, has emerged as a unique way to do chemistry with proteins. Herein, we report the reactivity engineering of SpyTag–SpyCatcher mutant pairs and show that distinct reactivity can be encrypted for the same r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627348/ https://www.ncbi.nlm.nih.gov/pubmed/28989685 http://dx.doi.org/10.1039/c7sc02686b |
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author | Liu, Yajie Liu, Dong Yang, Wei Wu, Xia-Ling Lai, Luhua Zhang, Wen-Bin |
author_facet | Liu, Yajie Liu, Dong Yang, Wei Wu, Xia-Ling Lai, Luhua Zhang, Wen-Bin |
author_sort | Liu, Yajie |
collection | PubMed |
description | Genetically encoded covalent peptide tagging technology, such as the SpyTag–SpyCatcher reaction, has emerged as a unique way to do chemistry with proteins. Herein, we report the reactivity engineering of SpyTag–SpyCatcher mutant pairs and show that distinct reactivity can be encrypted for the same reaction based on protein sequences of high similarity. Valuable features, including high selectivity, inverse temperature dependence and (nearly) orthogonal reactivity, could be achieved based on as few as three mutations. This demonstrates the robustness of the SpyTag–SpyCatcher reaction and the plasticity of its sequence specificity, pointing to a family of engineered protein chemistry tools. |
format | Online Article Text |
id | pubmed-5627348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56273482017-10-06 Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption Liu, Yajie Liu, Dong Yang, Wei Wu, Xia-Ling Lai, Luhua Zhang, Wen-Bin Chem Sci Chemistry Genetically encoded covalent peptide tagging technology, such as the SpyTag–SpyCatcher reaction, has emerged as a unique way to do chemistry with proteins. Herein, we report the reactivity engineering of SpyTag–SpyCatcher mutant pairs and show that distinct reactivity can be encrypted for the same reaction based on protein sequences of high similarity. Valuable features, including high selectivity, inverse temperature dependence and (nearly) orthogonal reactivity, could be achieved based on as few as three mutations. This demonstrates the robustness of the SpyTag–SpyCatcher reaction and the plasticity of its sequence specificity, pointing to a family of engineered protein chemistry tools. Royal Society of Chemistry 2017-09-01 2017-07-19 /pmc/articles/PMC5627348/ /pubmed/28989685 http://dx.doi.org/10.1039/c7sc02686b Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Liu, Yajie Liu, Dong Yang, Wei Wu, Xia-Ling Lai, Luhua Zhang, Wen-Bin Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption |
title | Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption
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title_full | Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption
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title_fullStr | Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption
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title_full_unstemmed | Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption
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title_short | Tuning SpyTag–SpyCatcher mutant pairs toward orthogonal reactivity encryption
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title_sort | tuning spytag–spycatcher mutant pairs toward orthogonal reactivity encryption |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627348/ https://www.ncbi.nlm.nih.gov/pubmed/28989685 http://dx.doi.org/10.1039/c7sc02686b |
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