Structural basis of BLyS receptor recognition

被引:67
|
作者
Oren, DA
Li, YL
Volovik, Y
Morris, TS
Dharia, C
Das, K
Galperina, O
Gentz, R
Arnold, E
机构
[1] Rutgers State Univ, Ctr Adv Biotechnol & Med, Piscataway, NJ 08816 USA
[2] Rutgers State Univ, Dept Chem & Biol Chem, Piscataway, NJ 08816 USA
[3] Dept Prot Dev, Rockville, MD 20850 USA
关键词
D O I
10.1038/nsb769
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
B lymphocyte stimulator (BLyS), a member of the tumor necrosis factor (TNF) superfamily, is a cytokine that induces B-cell proliferation and immunoglobulin secretion. We have determined the three-dimensional structure of BLyS to 2.0 Angstrom resolution and identified receptor recognition segments using limited proteolysis coupled with mass spectrometry. Similar to other structurally determined TNF-like ligands, the BLyS monomer is a beta-sandwich and oligomerizes to form a homotrimer. The receptor-binding region in BLyS is a deeper, more pronounced groove than in other cytokines. The conserved elements on the 'floor' of this groove allow for cytokine recognition of several structurally related receptors, whereas variations on the 'walls' and outer rims of the groove confer receptor specificity.
引用
收藏
页码:288 / 292
页数:5
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