Back to Search Start Over

Sialic Acid Glycoengineering Using an Unnatural Sialic Acid for the Detection of Sialoglycan Biosynthesis Defects and On-Cell Synthesis of Siglec Ligands

Authors :
Büll, Christian
Heise, Torben
Beurskens, Daniëlle M. H.
Riemersma, Moniek
Ashikov, Angel
Rutjes, Floris P. J. T.
van Kuppevelt, Toin H.
Lefeber, Dirk J.
den Brok, Martijn H.
Adema, Gosse J.
Boltje, Thomas J.
Source :
ACS Chemical Biology; January 2015, Vol. 10 Issue: 10 p2353-2363, 11p
Publication Year :
2015

Abstract

Sialoglycans play a vital role in physiology, and aberrant sialoglycan expression is associated with a broad spectrum of diseases. Since biosynthesis of sialoglycans is only partially regulated at the genetic level, chemical tools are crucial to study their function. Here, we report the development of propargyloxycarbonyl sialic acid (Ac5NeuNPoc) as a powerful tool for sialic acid glycoengineering. Ac5NeuNPoc showed strongly increased labeling efficiency and exhibited less toxicity compared to those of widely used mannosamine analogues in vitroand was also more efficiently incorporated into sialoglycans in vivo. Unlike mannosamine analogues, Ac5NeuNPoc was exclusively utilized in the sialoglycan biosynthesis pathway, allowing a genetic defect in sialic acid biosynthesis to be specifically detected. Furthermore, Ac5NeuNPoc-based sialic acid glycoengineering enabled the on-cell synthesis of high-affinity Siglec-7 ligands and the identification of a novel Siglec-2 ligand. Thus, Ac5NeuNPoc glycoengineering is a highly efficient, nontoxic, and selective approach to study and modulate sialoglycan interactions on living cells.

Details

Language :
English
ISSN :
15548929 and 15548937
Volume :
10
Issue :
10
Database :
Supplemental Index
Journal :
ACS Chemical Biology
Publication Type :
Periodical
Accession number :
ejs36524829
Full Text :
https://doi.org/10.1021/acschembio.5b00501