N-ACETYLNEURAMINIC ACID METHYL ESTER 2,4,7,8,9-PENTAACETATE

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CAS: 73208-82-9
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Synonyms: N-ACETYLNEURAMINIC ACID METHYL ESTER 2,4,7,8,9-PENTAACETATE

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David Crich

Wayne State University
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Chi-Huey Wong

Department of Chemistry and the Skaggs Institute for Chemical Biology
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Thomas J. Boltje

Radboud University Nijmegen
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Co-reporter: Christian Büll, Torben Heise, Daniëlle M. H. Beurskens, Moniek Riemersma, Angel Ashikov, Floris P. J. T. Rutjes, Toin H. van Kuppevelt, Dirk J. Lefeber, Martijn H. den Brok, Gosse J. Adema, and Thomas J. Boltje
pp: 2353
Publication Date(Web):August 4, 2015
DOI: 10.1021/acschembio.5b00501
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 vitro and 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.

Masayuki Sato

University of Shizuoka
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