Issue 37, 2024

Key role of cycloalkyne nature in alkyne-dye reagents for enhanced specificity of intracellular imaging by bioorthogonal bioconjugation

Abstract

Conjugates of benzothiophene-fused azacyclononyne BT9N-NH2 with fluorescent dyes were developed to visualise azidoglycans intracellularly. The significance of the cycloalkyne core was demonstrated by comparing new reagents with DBCO- and BCN-dye conjugates. To reduce non-specificity during intracellular bioconjugation using SPAAC, less reactive BT9N-dye reagents are preferred over highly reactive DBCO- and BCN-dye conjugates.

Graphical abstract: Key role of cycloalkyne nature in alkyne-dye reagents for enhanced specificity of intracellular imaging by bioorthogonal bioconjugation

Supplementary files

Article information

Article type
Paper
Submitted
20 Jun 2024
Accepted
02 Jul 2024
First published
03 Jul 2024
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2024,22, 7637-7642

Key role of cycloalkyne nature in alkyne-dye reagents for enhanced specificity of intracellular imaging by bioorthogonal bioconjugation

A. A. Vidyakina, S. A. Silonov, A. I. Govdi, A. Yu. Ivanov, E. P. Podolskaya, I. A. Balova, S. Bräse and N. A. Danilkina, Org. Biomol. Chem., 2024, 22, 7637 DOI: 10.1039/D4OB01032A

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