N-Azidoacetylmannosamine-mediated chemical tagging of gangliosides

被引:21
作者
Bussink, Anton P.
van Swieten, Paul F.
Ghauharali, Karen
Scheij, Saskia
van Eijk, Marco
Wennekes, Tom
van der Marel, Gijs A.
Boot, Rolf G.
Aerts, Johannes M. F. G.
Overkleeft, Herman S.
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Biochem, NL-1105 AZ Amsterdam, Netherlands
[2] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
关键词
N-acetylmannosamine; iminosugar; azide; Staudinger ligation; sialic acid; chemical ligation; cell surface labeling;
D O I
10.1194/jlr.C700006-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1417 / 1421
页数:5
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