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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...

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Autores principales: Crecente-Garcia, Selma, Neckebroeck, Albane, Clark, J. Stephen, Smith, Brian O., Thomson, Andrew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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
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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.
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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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