Click’n lock: rapid exchange between unsymmetric tetrazines and thiols for reversible, chemoselective functionalisation of biomolecules with on-demand bioorthogonal locking
Author:
Affiliation:
1. Systems Chemistry Department, Institute for Molecules and Materials, Radboud University Nijmegen, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands
Abstract
Funder
Radboud Universiteit
Publisher
Royal Society of Chemistry (RSC)
Subject
Biochemistry, Genetics and Molecular Biology (miscellaneous),Molecular Biology,Biochemistry,Chemistry (miscellaneous)
Link
http://pubs.rsc.org/en/content/articlepdf/2023/CB/D3CB00062A
Reference45 articles.
1. A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems
2. Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
3. Click Chemistry: Diverse Chemical Function from a Few Good Reactions
4. Click Chemistry in Materials Science
5. Click Chemistry and Material Selection for in Situ Fabrication of Hydrogels in Tissue Engineering Applications
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1. Accessing Functionalized Tetrazines as Click Chemistry Tools: A Synthesis Guide for Chemists and Chemical Biologists;European Journal of Organic Chemistry;2023-12-18
2. Recent Advances in Bioorthogonal Ligation and Bioconjugation;Topics in Current Chemistry;2023-11-22
3. Rapid, traceless and facile peptide cyclization enabled by tetrazine‐thiol exchange;Journal of Peptide Science;2023-10
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