High throughput platforms for structural genomics of integral membrane proteins

被引:20
作者
Mancia, Filippo [2 ]
Love, James [1 ]
机构
[1] New York Struct Biol Ctr, New York, NY USA
[2] Columbia Univ, Dept Physiol & Cellular Biophys, New York, NY USA
关键词
CRYSTAL-STRUCTURE; MYCOBACTERIUM-TUBERCULOSIS; COUPLED RECEPTORS; EXPRESSION; PURIFICATION; CLONING; STRATEGY; CHANNEL; ASSAY; PROTEOME;
D O I
10.1016/j.sbi.2011.07.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Structural genomics approaches on integral membrane proteins have been postulated for over a decade, yet specific efforts are lagging years behind their soluble counterparts. Indeed, high throughput methodologies for production and characterization of prokaryotic integral membrane proteins are only now emerging, while large-scale efforts for eukaryotic ones are still in their infancy. Presented here is a review of recent literature on actively ongoing structural genomics of membrane protein initiatives, with a focus on those aimed at implementing interesting techniques aimed at increasing our rate of success for this class of macromolecules.
引用
收藏
页码:517 / 522
页数:6
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