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Sequence-Specific 2-Cyanobenzothiazole Ligation
[Image: see text] The use of small, natural chemical reporters in conjunction with catalyst-free bioorthogonal reactions will greatly streamline protein labeling in a cellular environment with minimum perturbation to their function. Here we report the discovery of a 2-cyanobenzothiazole (CBT)-reacti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861237/ https://www.ncbi.nlm.nih.gov/pubmed/27082895 http://dx.doi.org/10.1021/jacs.6b00982 |
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author | Ramil, Carlo P. An, Peng Yu, Zhipeng Lin, Qing |
author_facet | Ramil, Carlo P. An, Peng Yu, Zhipeng Lin, Qing |
author_sort | Ramil, Carlo P. |
collection | PubMed |
description | [Image: see text] The use of small, natural chemical reporters in conjunction with catalyst-free bioorthogonal reactions will greatly streamline protein labeling in a cellular environment with minimum perturbation to their function. Here we report the discovery of a 2-cyanobenzothiazole (CBT)-reactive peptide tag, CX10R7, from a cysteine-encoded peptide phage library using the phage-assisted interrogation of reactivity method. Fusion of CX10R7 with a protein of interest allows site-specific labeling of the protein with CBT both in vitro and on the surface of E. coli cells. Mutagenesis studies indicated that the reactivity and specificity of CX10R7 are attributed to the sequence environment, in which the residues surrounding cysteine help to stabilize the ligation product. |
format | Online Article Text |
id | pubmed-4861237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48612372016-11-21 Sequence-Specific 2-Cyanobenzothiazole Ligation Ramil, Carlo P. An, Peng Yu, Zhipeng Lin, Qing J Am Chem Soc [Image: see text] The use of small, natural chemical reporters in conjunction with catalyst-free bioorthogonal reactions will greatly streamline protein labeling in a cellular environment with minimum perturbation to their function. Here we report the discovery of a 2-cyanobenzothiazole (CBT)-reactive peptide tag, CX10R7, from a cysteine-encoded peptide phage library using the phage-assisted interrogation of reactivity method. Fusion of CX10R7 with a protein of interest allows site-specific labeling of the protein with CBT both in vitro and on the surface of E. coli cells. Mutagenesis studies indicated that the reactivity and specificity of CX10R7 are attributed to the sequence environment, in which the residues surrounding cysteine help to stabilize the ligation product. American Chemical Society 2016-04-15 2016-05-04 /pmc/articles/PMC4861237/ /pubmed/27082895 http://dx.doi.org/10.1021/jacs.6b00982 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Ramil, Carlo P. An, Peng Yu, Zhipeng Lin, Qing Sequence-Specific 2-Cyanobenzothiazole Ligation |
title | Sequence-Specific
2-Cyanobenzothiazole Ligation |
title_full | Sequence-Specific
2-Cyanobenzothiazole Ligation |
title_fullStr | Sequence-Specific
2-Cyanobenzothiazole Ligation |
title_full_unstemmed | Sequence-Specific
2-Cyanobenzothiazole Ligation |
title_short | Sequence-Specific
2-Cyanobenzothiazole Ligation |
title_sort | sequence-specific
2-cyanobenzothiazole ligation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861237/ https://www.ncbi.nlm.nih.gov/pubmed/27082895 http://dx.doi.org/10.1021/jacs.6b00982 |
work_keys_str_mv | AT ramilcarlop sequencespecific2cyanobenzothiazoleligation AT anpeng sequencespecific2cyanobenzothiazoleligation AT yuzhipeng sequencespecific2cyanobenzothiazoleligation AT linqing sequencespecific2cyanobenzothiazoleligation |