The production, purification and crystallization of a soluble form of the nonclassical MHC HLA-G: the essential role of cobalt

被引:8
作者
Clements, CS
Kjer-Nielsen, L
Kostenko, L
McCluskey, J [1 ]
Rossjohn, J
机构
[1] Monash Univ, Sch Biomed Sci, Dept Biochem & Mol Biol, Prot Crystallog Unit, Clayton, Vic 3800, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
来源
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS | 2006年 / 62卷
关键词
D O I
10.1107/S1744309105041473
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
HLA-G is a nonclassical class I major histocompatibility complex (MHC) molecule that is primarily expressed at the foetal-maternal interface. Although the role of HLA-G has not been fully elucidated, current evidence suggests it protects the foetus from the maternal immune response. In this report, HLA-G ( 44 kDa) is characterized by expression in Escherichia coli. The inclusion bodies were refolded in complex with a peptide derived from histone H2A (RIIPRHLQL), purified and subsequently crystallized. Correct refolding was determined using two conformation-dependent antibodies. Cobalt ions were shown to be an essential ingredient for obtaining diffraction-quality crystals. The crystals, which diffracted to 1.9 angstrom resolution, belonged to space group P3(2)2(1), with unit-cell parameters a = b = 77.15, c = 151.72 angstrom.
引用
收藏
页码:70 / 73
页数:4
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