Analysis and Optimization of Copper-Catalyzed Azide-Alkyne Cycloaddition for Bioconjugation

How to click with biomolecules: Copper‐catalyzed azide–alkyne cycloaddition has been optimized for use with biological molecules. The key development is the addition of two reagents that allow ascorbate to be used as reducing agent whilst eliminating problems caused by copper ascorbate side reaction...

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Veröffentlicht in:Angewandte Chemie (International ed.) 2009-01, Vol.48 (52), p.9879-9883
Hauptverfasser: Hong, Vu, Presolski, Stanislav I, Ma, Celia, Finn, M.G
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container_end_page 9883
container_issue 52
container_start_page 9879
container_title Angewandte Chemie (International ed.)
container_volume 48
creator Hong, Vu
Presolski, Stanislav I
Ma, Celia
Finn, M.G
description How to click with biomolecules: Copper‐catalyzed azide–alkyne cycloaddition has been optimized for use with biological molecules. The key development is the addition of two reagents that allow ascorbate to be used as reducing agent whilst eliminating problems caused by copper ascorbate side reactions. The result is a robust, rapid, and convenient procedure for the modification of proteins, DNA, RNA, and other biomolecules (see scheme).
doi_str_mv 10.1002/anie.200905087
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source MEDLINE; Wiley Online Library All Journals
subjects alkynes
Alkynes - chemistry
Allolevivirus - chemistry
Ascorbic Acid - chemistry
azides
Azides - chemistry
bioconjugation
Catalysis
copper
Copper - chemistry
cycloaddition
RNA - chemistry
Serum Albumin, Bovine - chemistry
title Analysis and Optimization of Copper-Catalyzed Azide-Alkyne Cycloaddition for Bioconjugation
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