Rapid one-pot iterative diselenide–selenoester ligation using a novel coumarin-based photolabile protecting group-Reference-Cited by-同舟云学术

Rapid one-pot iterative diselenide–selenoester ligation using a novel coumarin-based photolabile protecting group

Published:2021 Issue:29 Volume:12 Page:10014-10021
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Kambanis Lucas¹²³⁴⁵^ORCID,Chisholm Timothy S.¹²³⁴⁵^ORCID,Kulkarni Sameer S.¹²³⁴⁵^ORCID,Payne Richard J.¹²³⁴⁵^ORCID

Affiliation:

1. School of Chemistry

2. The University of Sydney

3. Sydney

4. Australia

5. Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science

Abstract

A method for the rapid one-pot iterative assembly of proteins via diselenide–selenoester ligation (DSL) chemistry is described that capitalises on a novel coumarin-based photolabile protecting group for selenocysteine.

Funder

Australian Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/SC/D1SC02781F

Reference47 articles.

1. Total chemical synthesis of proteins

2. Expanding the chemical toolbox for the synthesis of large and uniquely modified proteins

3. Rapid and efficient protein synthesis through expansion of the native chemical ligation concept

4. Native chemical ligation in protein synthesis and semi-synthesis

5. Synthesis of Proteins by Native Chemical Ligation

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