Expression of the Arabidopsis G-protein GPα1: purification and characterisation of the recombinant protein

被引:0
|
作者
Alan Wise
Paul G. Thomas
T. Hedley Carr
Gillian A. Murphy
Paul A. Millner*
机构
[1] University of Glasgow,Molecular Pharmacology Group, Department of Biochemistry
[2] Jealott's Hill Research Station,Zeneca Agrochemicals
[3] University of Leeds,Department of Biochemistry and Molecular Biology
来源
Plant Molecular Biology | 1997年 / 33卷
关键词
affinity chromatography; GPα1; G-protein; dnaY; GTPγS binding; metal ions;
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学科分类号
摘要
The Arabidopsis Gα subunit, GPα1, was expressedwithin Escherichia coli by co-transformation with the expressionvector and the dnaY gene which encodes tRNAArgAGA/AGG. Isolation of the recombinant GPα1 in a highly pureform could be achieved by a combination of anion exchange and dyeaffinity chromatography or by a single step affinity procedure viachromatography on 4-amino-anilido-GTP agarose. The recombinant proteinyielded by both procedures was highly active and bound GTPγS withan apparent Kd in the nM range. GTPγS binding wasstimulated two-fold in the presence of Zn2+ compared with that inthe presence of Mg2+, Mn2+ or Ca2+.Abbreviations: 4aaGTP, 4-amino-anilido-GTP; GTPγS,guanosine- 5′-(3-O-thiotriphosphate), PMSF,phenylmethylsulphonyl fluoride; PVDF, polvinylidene fluoride;rGPα1, recombinant GPα1
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页码:723 / 728
页数:5
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