3G08

Crystal structure of the alpha-galactosylceramide analog OCH in complex with mouse CD1d

3G08 の概要

• エントリーDOI: 10.2210/pdb3g08/pdb
• 関連するPDBエントリー: 1Z5L 1zt4
• 分子名称: T-cell surface glycoprotein CD1d1, Beta-2 microglobulin, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total)
• 機能のキーワード: antigen presentation, glycolipid, nkt cells, cell membrane, endosome, glycoprotein, immune response, immunoglobulin domain, innate immunity, lysosome, membrane, transmembrane, mhc i, secreted, immune system
• 由来する生物種: Mus musculus (mouse); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 46120.29

構造登録者

Zajonc, D.M. (登録日: 2009-01-27, 公開日: 2009-12-08, 最終更新日: 2024-10-16)

主引用文献

Sullivan, B.A.,Nagarajan, N.A.,Wingender, G.,Wang, J.,Scott, I.,Tsuji, M.,Franck, R.W.,Porcelli, S.A.,Zajonc, D.M.,Kronenberg, M.
Mechanisms for glycolipid antigen-driven cytokine polarization by Valpha14i NKT cells.
J.Immunol., 184:141-153, 2010

PubMed Abstract: Certain glycolipid Ags for Valpha14i NKT cells can direct the overall cytokine balance of the immune response. Th2-biasing OCH has a lower TCR avidity than the most potent agonist known, alpha-galactosylceramide. Although the CD1d-exposed portions of OCH and alpha-galactosylceramide are identical, structural analysis indicates that there are subtle CD1d conformational differences due to differences in the buried lipid portion of these two Ags, likely accounting for the difference in antigenic potency. Th1-biasing C-glycoside/CD1d has even weaker TCR interactions than OCH/CD1d. Despite this, C-glycoside caused a greater downstream activation of NK cells to produce IFN-gamma, accounting for its promotion of Th1 responses. We found that this difference correlated with the finding that C-glycoside/CD1d complexes survive much longer in vivo. Therefore, we suggest that the pharmacokinetic properties of glycolipids are a major determinant of cytokine skewing, suggesting a pathway for designing therapeutic glycolipids for modulating invariant NKT cell responses.

PubMed: 19949076
DOI: 10.4049/jimmunol.0902880

実験手法

X-RAY DIFFRACTION (1.6 Å)