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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...

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Autores principales: Ramil, Carlo P., An, Peng, Yu, Zhipeng, Lin, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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
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