Title of article :
Crystal Structure of sTALL-1 Reveals a Virus-like Assembly of TNF Family Ligands
Author/Authors :
Yingfang Liu، نويسنده , , Liangguo Xu، نويسنده , , Natasha Opalka، نويسنده , , John Kappler، نويسنده , , Hong-Bing Shu، نويسنده , , Gongyi Zhang، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
12
From page :
383
To page :
394
Abstract :
TALL-1/BAFF/BLyS was recently identified as a member of the tumor necrosis factor (TNF) ligand family. The crystal structure of the functional soluble TALL-1 (sTALL-1) has been determined at 3.0 Å. sTALL-1 forms a virus-like assembly with 200 Å diameter in the crystals, containing 60 sTALL-1 monomers. The cluster formation is mediated by a “flap” region of the sTALL-1 monomer. The virus-like assembly was also detected in solution using gel filtration and electron microscopy. Deletion of the flap region disrupted the formation of the virus-like assembly. The mutant sTALL-1 still bound its receptor but could not activate NF-κB and did not stimulate B lymphocyte proliferation. Finally, we found the virus-like cluster of sTALL-1 exists in physiological condition. We propose that this virus-like assembly of sTALL-1 is the functional unit for TALL-1 in vivo.
Journal title :
CELL
Serial Year :
2002
Journal title :
CELL
Record number :
1017678
Link To Document :
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