Structural basis for selective recognition of oligosaccharides by DC-SIGN and DC-SIGNR

被引:564
作者
Feinberg, H
Mitchell, DA
Drickamer, K
Weis, WI [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Biol Struct, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Stanford, CA 94305 USA
[3] Univ Oxford, Dept Biochem, Glycobiol Inst, Oxford OX1 3QU, England
关键词
D O I
10.1126/science.1066371
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dendritic cell specific intracellular adhesion molecule-3 (ICAM-3) grabbing nonintegrin (DC-SIGN), a C-type lectin present on the surface of dendritic cells, mediates the initial interaction of dendritic cells with T cells by binding to ICAM-3. DC-SIGN and DC-SIGNR, a related receptor found on the endothelium of Liver sinusoids, placental capillaries, and Lymph nodes, bind to oligosaccharides that are present on the envelope of human immunodeficiency virus (HIV), an interaction that strongly promotes viral infection of T cells. Crystal structures of carbohydrate-recognition domains of DC-SIGN and of DC-SIGNR bound to oligosaccharide, in combination with binding studies, reveal that these receptors selectively recognize endogenous high-mannose oligosaccharides and may represent a new avenue for developing HIV prophylactics.
引用
收藏
页码:2163 / 2166
页数:4
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