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β-Turn Mimics by Chemical Ligation
[Image: see text] We report a simple reductive amination protocol to ligate two peptides, while simultaneously installing a β-turn mimic at the ligation junction. This strategy uses commercially available materials, mild chemical conditions, and a chemoselective ligation reaction of unprotected pept...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304061/ https://www.ncbi.nlm.nih.gov/pubmed/32406695 http://dx.doi.org/10.1021/acs.orglett.0c01427 |
_version_ | 1783548190002249728 |
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author | Crecente-Garcia, Selma Neckebroeck, Albane Clark, J. Stephen Smith, Brian O. Thomson, Andrew R. |
author_facet | Crecente-Garcia, Selma Neckebroeck, Albane Clark, J. Stephen Smith, Brian O. Thomson, Andrew R. |
author_sort | Crecente-Garcia, Selma |
collection | PubMed |
description | [Image: see text] We report a simple reductive amination protocol to ligate two peptides, while simultaneously installing a β-turn mimic at the ligation junction. This strategy uses commercially available materials, mild chemical conditions, and a chemoselective ligation reaction of unprotected peptide substrates accessed through standard solid phase methods. This system was implemented in a designed β-hairpin system, and biophysical analysis demonstrates effective mimicry of the β-turn. |
format | Online Article Text |
id | pubmed-7304061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73040612020-06-19 β-Turn Mimics by Chemical Ligation Crecente-Garcia, Selma Neckebroeck, Albane Clark, J. Stephen Smith, Brian O. Thomson, Andrew R. Org Lett [Image: see text] We report a simple reductive amination protocol to ligate two peptides, while simultaneously installing a β-turn mimic at the ligation junction. This strategy uses commercially available materials, mild chemical conditions, and a chemoselective ligation reaction of unprotected peptide substrates accessed through standard solid phase methods. This system was implemented in a designed β-hairpin system, and biophysical analysis demonstrates effective mimicry of the β-turn. American Chemical Society 2020-05-14 2020-06-05 /pmc/articles/PMC7304061/ /pubmed/32406695 http://dx.doi.org/10.1021/acs.orglett.0c01427 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Crecente-Garcia, Selma Neckebroeck, Albane Clark, J. Stephen Smith, Brian O. Thomson, Andrew R. β-Turn Mimics by Chemical Ligation |
title | β-Turn Mimics by Chemical Ligation |
title_full | β-Turn Mimics by Chemical Ligation |
title_fullStr | β-Turn Mimics by Chemical Ligation |
title_full_unstemmed | β-Turn Mimics by Chemical Ligation |
title_short | β-Turn Mimics by Chemical Ligation |
title_sort | β-turn mimics by chemical ligation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304061/ https://www.ncbi.nlm.nih.gov/pubmed/32406695 http://dx.doi.org/10.1021/acs.orglett.0c01427 |
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