Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization

The selective formation of protein bioconjugates under physiological conditions is a challenging task. Here, the authors report that 1,4-dinitroimidazoles are reagents of choice for protein bioconjugation at either cysteine or lysine sites within short times and provide facile access to peptide macr...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Qunfeng Luo, Youqi Tao, Wangjian Sheng, Jingxia Lu, Huan Wang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2019
Materias:
Q
Acceso en línea:https://doaj.org/article/c3df2b6ef44148c49531f577004f9225
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:c3df2b6ef44148c49531f577004f9225
record_format dspace
spelling oai:doaj.org-article:c3df2b6ef44148c49531f577004f92252021-12-02T17:31:22ZDinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization10.1038/s41467-018-08010-22041-1723https://doaj.org/article/c3df2b6ef44148c49531f577004f92252019-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-08010-2https://doaj.org/toc/2041-1723The selective formation of protein bioconjugates under physiological conditions is a challenging task. Here, the authors report that 1,4-dinitroimidazoles are reagents of choice for protein bioconjugation at either cysteine or lysine sites within short times and provide facile access to peptide macrocycles.Qunfeng LuoYouqi TaoWangjian ShengJingxia LuHuan WangNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Qunfeng Luo
Youqi Tao
Wangjian Sheng
Jingxia Lu
Huan Wang
Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
description The selective formation of protein bioconjugates under physiological conditions is a challenging task. Here, the authors report that 1,4-dinitroimidazoles are reagents of choice for protein bioconjugation at either cysteine or lysine sites within short times and provide facile access to peptide macrocycles.
format article
author Qunfeng Luo
Youqi Tao
Wangjian Sheng
Jingxia Lu
Huan Wang
author_facet Qunfeng Luo
Youqi Tao
Wangjian Sheng
Jingxia Lu
Huan Wang
author_sort Qunfeng Luo
title Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
title_short Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
title_full Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
title_fullStr Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
title_full_unstemmed Dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
title_sort dinitroimidazoles as bifunctional bioconjugation reagents for protein functionalization and peptide macrocyclization
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/c3df2b6ef44148c49531f577004f9225
work_keys_str_mv AT qunfengluo dinitroimidazolesasbifunctionalbioconjugationreagentsforproteinfunctionalizationandpeptidemacrocyclization
AT youqitao dinitroimidazolesasbifunctionalbioconjugationreagentsforproteinfunctionalizationandpeptidemacrocyclization
AT wangjiansheng dinitroimidazolesasbifunctionalbioconjugationreagentsforproteinfunctionalizationandpeptidemacrocyclization
AT jingxialu dinitroimidazolesasbifunctionalbioconjugationreagentsforproteinfunctionalizationandpeptidemacrocyclization
AT huanwang dinitroimidazolesasbifunctionalbioconjugationreagentsforproteinfunctionalizationandpeptidemacrocyclization
_version_ 1718380637371498496