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Structural basis of BLyS receptor recognition.

Authors :
Oren, Deena A.
Li, Yuling
Volovik, Yulia
Morris, Tina S.
Dharia, Chhaya
Das, Kalyan
Galperina, Olga
Gentz, Reiner
Arnold, Eddy
Source :
Nature Structural Biology; Apr2002, Vol. 9 Issue 4, p288, 5p
Publication Year :
2002

Abstract

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 Å 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 β-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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10728368
Volume :
9
Issue :
4
Database :
Complementary Index
Journal :
Nature Structural Biology
Publication Type :
Academic Journal
Accession number :
8781934
Full Text :
https://doi.org/10.1038/nsb769