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Enzyme-Catalyzed Macrocyclization of Long Unprotected Peptides
[Image: see text] A glutathione S-transferase (GST) catalyzed macrocyclization reaction for peptides up to 40 amino acids in length is reported. GST catalyzes the selective S(N)Ar reaction between an N-terminal glutathione (GSH, γ-Glu-Cys-Gly) tag and a C-terminal perfluoroaryl-modified cysteine on...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372082/ https://www.ncbi.nlm.nih.gov/pubmed/25002256 http://dx.doi.org/10.1021/ol501609y |
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author | Zhang, Chi Dai, Peng Spokoyny, Alexander M. Pentelute, Bradley L. |
author_facet | Zhang, Chi Dai, Peng Spokoyny, Alexander M. Pentelute, Bradley L. |
author_sort | Zhang, Chi |
collection | PubMed |
description | [Image: see text] A glutathione S-transferase (GST) catalyzed macrocyclization reaction for peptides up to 40 amino acids in length is reported. GST catalyzes the selective S(N)Ar reaction between an N-terminal glutathione (GSH, γ-Glu-Cys-Gly) tag and a C-terminal perfluoroaryl-modified cysteine on the same polypeptide chain. Cyclic peptides ranging from 9 to 24 residues were quantitatively produced within 2 h in aqueous pH = 8 buffer at room temperature. The reaction was highly selective for cyclization at the GSH tag, enabling the combination of GST-catalyzed ligation with native chemical ligation to generate a large 40-residue peptide macrocycle. |
format | Online Article Text |
id | pubmed-4372082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43720822015-07-08 Enzyme-Catalyzed Macrocyclization of Long Unprotected Peptides Zhang, Chi Dai, Peng Spokoyny, Alexander M. Pentelute, Bradley L. Org Lett [Image: see text] A glutathione S-transferase (GST) catalyzed macrocyclization reaction for peptides up to 40 amino acids in length is reported. GST catalyzes the selective S(N)Ar reaction between an N-terminal glutathione (GSH, γ-Glu-Cys-Gly) tag and a C-terminal perfluoroaryl-modified cysteine on the same polypeptide chain. Cyclic peptides ranging from 9 to 24 residues were quantitatively produced within 2 h in aqueous pH = 8 buffer at room temperature. The reaction was highly selective for cyclization at the GSH tag, enabling the combination of GST-catalyzed ligation with native chemical ligation to generate a large 40-residue peptide macrocycle. American Chemical Society 2014-07-08 2014-07-18 /pmc/articles/PMC4372082/ /pubmed/25002256 http://dx.doi.org/10.1021/ol501609y Text en Copyright © 2014 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 | Zhang, Chi Dai, Peng Spokoyny, Alexander M. Pentelute, Bradley L. Enzyme-Catalyzed Macrocyclization of Long Unprotected Peptides |
title | Enzyme-Catalyzed Macrocyclization of Long Unprotected
Peptides |
title_full | Enzyme-Catalyzed Macrocyclization of Long Unprotected
Peptides |
title_fullStr | Enzyme-Catalyzed Macrocyclization of Long Unprotected
Peptides |
title_full_unstemmed | Enzyme-Catalyzed Macrocyclization of Long Unprotected
Peptides |
title_short | Enzyme-Catalyzed Macrocyclization of Long Unprotected
Peptides |
title_sort | enzyme-catalyzed macrocyclization of long unprotected
peptides |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372082/ https://www.ncbi.nlm.nih.gov/pubmed/25002256 http://dx.doi.org/10.1021/ol501609y |
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