Fisher M T
Department of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City 66160-7421.
J Biol Chem. 1994 May 6;269(18):13629-36.
The yields of active dodecameric glutamine synthetase (GS) are significantly increased when in vitro folding is initiated in the presence of the Escherichia coli groE chaperonins and ATP (37 degrees C). To observe the effects of chaperonins and ATP on GS assembly, the GS assembly intermediates were separated by nondenaturing gel electrophoresis, visualized by Western analysis, and studied as a function of time. The form of GS that was initially released from groEL is monomeric. After the monomers formed dimers, active GS oligomers were assembled by the association of assembly competent dimers with higher order even-numbered oligomers until the dodecamer was formed. When ATP was added to the groEL.GS complex (no groES), a groEL.GS complex remained visible for up to 30 min after the renaturation was initiated. This slow disappearance of the groEL.GS complex is consistent with observed lags in both the GS activity regain profile and the assembly-dependent increase in GS tryptophan fluorescence. When groES was present, the addition of ATP resulted in the disappearance of observable complex at early sample times (< 2 min). Concomitantly, the rates of the regain of GS activity and the GS-dependent increase in tryptophan fluorescence intensity showed substantial accelerations. These results indicate that groES facilitates GS assembly from groEL by inducing the rapid release of GS from groEL, which in turn increases the concentration of assembly competent GS monomers. In addition, groES can initiate renaturation of GS from the groEL.GS arrested complex in the presence of ADP. When chaperonin-dependent GS renaturation was initiated with ATP or ADP (> or = 2 mM), the rates were identical. Since ATP hydrolysis is not absolutely required, the combined binding energies of groES and ATP (or ADP) appear to be sufficient to weaken the binding affinity of groEL for GS subunits and facilitate the release and refolding of assembly competent GS monomers from groEL.
当在大肠杆菌groE伴侣蛋白和ATP(37摄氏度)存在的情况下启动体外折叠时,活性十二聚体谷氨酰胺合成酶(GS)的产量会显著增加。为了观察伴侣蛋白和ATP对GS组装的影响,通过非变性凝胶电泳分离GS组装中间体,用蛋白质免疫印迹法进行可视化,并作为时间的函数进行研究。最初从groEL释放的GS形式是单体。单体形成二聚体后,活性GS寡聚体通过具有组装能力的二聚体与更高阶偶数寡聚体的缔合而组装,直到形成十二聚体。当向groEL.GS复合物(无groES)中添加ATP时,在复性开始后长达30分钟内,groEL.GS复合物仍然可见。groEL.GS复合物的这种缓慢消失与GS活性恢复曲线以及GS色氨酸荧光中依赖组装的增加所观察到的滞后现象一致。当存在groES时,添加ATP导致在早期样品时间(<2分钟)可观察到的复合物消失。同时,GS活性恢复率和GS依赖的色氨酸荧光强度增加率显示出显著加速。这些结果表明,groES通过诱导GS从groEL快速释放来促进从groEL的GS组装,这反过来又增加了具有组装能力的GS单体的浓度。此外,在ADP存在的情况下,groES可以启动从groEL.GS停滞复合物的GS复性。当用ATP或ADP(≥2 mM)启动依赖伴侣蛋白的GS复性时,速率是相同的。由于ATP水解不是绝对必需的,groES和ATP(或ADP)的结合能总和似乎足以削弱groEL对GS亚基的结合亲和力,并促进具有组装能力的GS单体从groEL的释放和重折叠。