Wynn R M, Davie J R, Cox R P, Chuang D T
Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 75235.
J Biol Chem. 1992 Jun 25;267(18):12400-3.
We have investigated the possible role of chaperonins groEL and groES in the folding and assembly of heterotetramers (alpha 2 beta 2) of mammalian mitochondrial branched-chain alpha-keto acid decarboxylase (E1) in Escherichia coli. The mature E1 alpha subunit fused to maltose-binding protein (MBP) was coexpressed with mature E1 beta on the same vector in ES- and EL- mutant strains. Only small or trace amounts of active E1 component were obtained. Cotransformation of the ES- mutant host with a second vector overexpressing groEL and groES resulted in a greater than 500-fold increase in E1-specific activity. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that the content of both MBP-E1 alpha and E1 beta polypeptides was markedly increased in the presence of overexpressed chaperonin proteins. The time course studies showed that the increase in E1-specific activity and subunit levels correlated with the increase in groEL and groES until the concentration of the chaperonins reached a saturating level in the cell. The functional MBP-E1 fusion protein from ES- double transformants were purified by amylose resin affinity chromatography. The MBP moiety was removed by subsequent digestion with Factor Xa endoprotease, followed by Sephacryl S-300HR chromatography. It was found that E1 alpha and E1 beta assembled into an active 160-kDa species, which was consistent with the alpha 2 beta 2 structure of E1. The present results demonstrate that chaperonins groEL and groES promote folding and assembly of heterotetrameric proteins of mammalian mitochondrial origin.
我们研究了伴侣蛋白groEL和groES在大肠杆菌中对哺乳动物线粒体支链α-酮酸脱羧酶(E1)异源四聚体(α2β2)折叠和组装过程中可能发挥的作用。与麦芽糖结合蛋白(MBP)融合的成熟E1α亚基与成熟E1β在同一载体上于ES - 和EL - 突变菌株中共同表达。仅获得了少量或痕量的活性E1组分。用过量表达groEL和groES的第二个载体对ES - 突变宿主进行共转化,导致E1特异性活性增加了500倍以上。十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳显示,在过量表达伴侣蛋白的情况下,MBP - E1α和E1β多肽的含量均显著增加。时间进程研究表明,E1特异性活性和亚基水平的增加与groEL和groES的增加相关,直到伴侣蛋白在细胞中的浓度达到饱和水平。来自ES - 双转化体的功能性MBP - E1融合蛋白通过直链淀粉树脂亲和层析进行纯化。随后用Xa因子内切蛋白酶消化去除MBP部分,接着进行Sephacryl S - 300HR层析。结果发现,E1α和E1β组装成了一个活性的160 kDa物种,这与E1的α2β2结构一致。目前的结果表明,伴侣蛋白groEL和groES促进了哺乳动物线粒体来源的异源四聚体蛋白的折叠和组装。