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果蝇26S蛋白酶体的组装伴随着广泛的亚基重排。

Assembly of the Drosophila 26 S proteasome is accompanied by extensive subunit rearrangements.

作者信息

Kurucz Eva, Andó István, Sümegi Máté, Hölzl Harald, Kapelari Barbara, Baumeister Wolfgang, Udvardy Andor

机构信息

Biological Research Center of the Hungarian Academy of Sciences, P.O. Box 521, H-6701 Szeged, Hungary.

出版信息

Biochem J. 2002 Jul 15;365(Pt 2):527-36. doi: 10.1042/BJ20011520.

Abstract

The subunit contacts in the regulatory complex of the Drosophila 26 S proteasome were studied through the cross-linking of closely spaced subunits of the complex, and analysis of the cross-linking pattern in an immunoblot assay with the use of subunit-specific monoclonal antibodies. The cross-linking pattern of the purified 26 S proteasome exhibits significant differences as compared with that of the purified free regulatory complex. It is shown that the observed differences are due to extensive rearrangement of the subunit contacts accompanying the assembly of the 26 S proteasome from the regulatory complex and the 20 S proteasome. Cross-linking studies and electron microscopic examinations revealed that these changes are reversible and follow the assembly or the disassembly of the 26 S proteasome. Although the majority of the changes observed in the subunit contacts affected the hexameric ring of the ATPase subunits, the alterations extended over the whole of the regulatory complex, affecting subunit contacts even in the lid subcomplex. Changes in the subunit contacts, similar to those in the regulatory complex, were detected in the 20 S proteasome. These observations indicate that the assembly of the 26 S proteasome is not simply a passive docking of two rigid subcomplexes. In the course of the assembly, the interacting subcomplexes mutually rearrange their structures so as to create the optimal conformation required for the assembly and the proper functioning of the 26 S proteasome.

摘要

通过对果蝇26S蛋白酶体调节复合物中紧密相邻亚基进行交联,并利用亚基特异性单克隆抗体在免疫印迹分析中分析交联模式,对该调节复合物中的亚基接触进行了研究。与纯化的游离调节复合物相比,纯化的26S蛋白酶体的交联模式显示出显著差异。结果表明,观察到的差异是由于在26S蛋白酶体从调节复合物和20S蛋白酶体组装过程中,亚基接触发生了广泛的重排。交联研究和电子显微镜检查表明,这些变化是可逆的,并且伴随着26S蛋白酶体的组装或拆卸。虽然在亚基接触中观察到的大多数变化影响了ATP酶亚基的六聚体环,但这些改变扩展到了整个调节复合物,甚至影响了盖子亚复合物中的亚基接触。在20S蛋白酶体中也检测到了与调节复合物中类似的亚基接触变化。这些观察结果表明,26S蛋白酶体的组装并非简单地是两个刚性亚复合物的被动对接。在组装过程中,相互作用的亚复合物相互重排其结构,以形成26S蛋白酶体组装和正常功能所需的最佳构象。

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