4.6 Article

N-Azidoacetylmannosamine-mediated chemical tagging of gangliosides

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JOURNAL OF LIPID RESEARCH
卷 48, 期 6, 页码 1417-1421

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DOI: 10.1194/jlr.C700006-JLR200

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N-acetylmannosamine; iminosugar; azide; Staudinger ligation; sialic acid; chemical ligation; cell surface labeling

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Peracetylated N-alpha-azidoacetylmannosamine (Ac(4)ManNAz) is metabolized by cells to CMP-azidosialic acid. It has been demonstrated previously that in this way azidosialic acid-containing glycoproteins are formed that can be labeled on the cell surface by a modified Staudinger ligation. Here, we first demonstrate that the same procedure also results in the formation of azidosialic acid-containing gangliosides. Deoxymannojirimycin, an inhibitor of N-glycan processing in proteins, decreases the total cell surface labeling in Jurkat cells by similar to 25%. Inhibition of ganglioside biosynthesis with N-[5-(adamantan-1-yl-methoxy)-pentyl]1-deoxynojirimycin reduces cell surface labeling by similar to 75%. In conclusion, exposure of cells to Ac(4)ManNAz allows in vivo chemical tagging of gangliosides.

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