4.8 Article

Crystal structure of sTALL-1 reveals a virus-like assembly of TNF family ligands

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CELL
卷 108, 期 3, 页码 383-394

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CELL PRESS
DOI: 10.1016/S0092-8674(02)00631-1

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  1. NIAID NIH HHS [AI49992] Funding Source: Medline
  2. NIGMS NIH HHS [GM65341] Funding Source: Medline

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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 Angstrom. sTALL-1 forms a virus-like assembly with 200 Angstrom 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-kappaB 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.

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