期刊
JOURNAL OF EXPERIMENTAL MEDICINE
卷 202, 期 11, 页码 1517-1526出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20051625
关键词
-
Sulfatide derived from the myelin stimulates a distinct population of CD1d- restricted natural killer T ( NKT) cells. Cis- tetracosenoyl sulfatide is one of the immunodominant species in myelin as identified by proliferation, cytokine secretion, and CD1d tetramer staining. The crystal structure of mouse CD1d in complex with cis- tetracosenoyl sulfatide at 1.9 angstrom resolution reveals that the longer cis- tetracosenoyl fatty acid chain fully occupies the A ' pocket of the CD1d binding groove, whereas the sphingosine chain fills up the F ' pocket. A precise hydrogen bond network in the center of the binding groove orients and positions the ceramide backbone for insertion of the lipid tails in their respective pockets. The 3 ' sulfated galactose headgroup is highly exposed for presentation to the T cell receptor and projects up and away from the binding pocket due to its beta linkage, compared with the more intimate binding of the alpha - glactosyl ceramide headgroup to CD1d. These structure and binding data on sulfatide presentation by CD1d have important implications for the design of therapeutics that target T cells reactive for myelin glycolipids in autoimmune diseases of the central nervous system.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据