Crystallization of protein-ligand complexes

被引:114
作者
Hassell, Anne M.
An, Gang
Bledsoe, Randy K.
Bynum, Jane M.
Carter, H. Luke, III
Deng, Su-Jun J.
Gampe, Robert T.
Grisard, Tamara E.
Madauss, Kevin P.
Nolte, Robert T.
Rocque, Warren J.
Wang, Liping
Weaver, Kurt L.
Williams, Shawn P.
Wisely, G. Bruce
Xu, Robert
Shewchuk, Lisa M.
机构
[1] GlaxoSmithKline Inc, Dept Comp Analyt & Struct Sci, Res Triangle Pk, NC 27709 USA
[2] GlaxoSmithKline Inc, Dept Gene Express Prot Biochem, Res Triangle Pk, NC 27709 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY | 2007年 / 63卷
关键词
D O I
10.1107/S0907444906047020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Obtaining diffraction-quality crystals has long been a bottleneck in solving the three-dimensional structures of proteins. Often proteins may be stabilized when they are complexed with a substrate, nucleic acid, cofactor or small molecule. These ligands, on the other hand, have the potential to induce significant conformational changes to the protein and ab initio screening may be required to find a new crystal form. This paper presents an overview of strategies in the following areas for obtaining crystals of protein-ligand complexes: (i) co-expression of the protein with the ligands of interest, (ii) use of the ligands during protein purification, (iii) cocrystallization and (iv) soaks.
引用
收藏
页码:72 / 79
页数:8
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