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  2. Amplified Visualization of Protein-Specific Glycosylation in Zebrafish via Proximity-Induced Hybridization Chain Reaction

Amplified Visualization of Protein-Specific Glycosylation in Zebrafish via Proximity-Induced Hybridization Chain Reaction

  • J Am Chem Soc. 2018 Dec 5;140(48):16589-16595. doi: 10.1021/jacs.8b08442.
Jingying Li 1 Shuya Liu 1 Liqin Sun 1 Wei Li 1 Su-Yun Zhang 2 Sheng Yang 2 Juan Li 3 Huang-Hao Yang 1 3
Affiliations

Affiliations

  • 1 College of Biological Science and Engineering , Fuzhou University , Fuzhou 350116 , P. R. China.
  • 2 Department of Medical Oncology , Fujian Medical University Union Hospital , Fuzhou 350001 , P. R. China.
  • 3 MOE Key Laboratory for Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection Technology for Food Safety, State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry , Fuzhou University , Fuzhou 350116 , P. R. China.
Abstract

The visualization of glycosylation states of specific proteins in vivo is of great importance for uncovering their roles in disease development. However, the ubiquity of glycosylation makes probing the glycans on a certain protein as difficult as looking for a needle in a haystack. Herein, we demonstrate a proximity-induced hybridization chain reaction (HCR) strategy for amplified visualization of protein-specific glycosylation. The strategy relies on designing two kinds of DNA probes, glycan conversion probes and protein recognition probes, which are attached to glycans and target proteins, respectively. Upon sequential binding to the targets, the proximity-induced hybridization between two probes occurs, which leads to the structure-switching of protein recognition probes, followed by triggering of HCR assembly. This strategy has been used to visualize tyrosine-protein kinase 7-specific sialic acid in living CEM cells and zebrafish and to monitor its variation during drug treatment. It provides a potential tool for investigating protein-specific glycosylation and researching the relation between dynamic glycans state and disease process.

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