Herzog Franz, Peters Jan-Michael
Research Institute of Molecular Pathology (IMP), 1030 Vienna, Austria.
Methods Enzymol. 2005;398:175-95. doi: 10.1016/S0076-6879(05)98016-6.
The anaphase-promoting complex or cyclosome (APC/C) is a ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle. The APC/C is a 1.5-MDa complex composed of at least 12 different core subunits. At different stages of mitosis and G1, the APC/C associates with a variety of regulatory proteins, such as the activator proteins Cdc20 and Cdh1 and the mitotic checkpoint complex (MCC), which regulate APC/C activity in a substrate-specific manner. Although APC/C and its regulators have been under intense investigation, it is still poorly understood how substrates are recognized and ubiquitinated by the APC/C, why so many subunits are required for these processes, and how regulators of the APC/C control its ubiquitin ligase activity in a substrate-specific manner. This chapter describes a simple and rapid procedure that allows the isolation of APC/C from vertebrate cells and tissues with reasonable purity and at high concentrations, yielding up to 0.5 mg of APC/C. This procedure should facilitate biochemical, biophysical, and structural analyses of the APC/C that will be needed for a better mechanistic understanding of its function and regulation.
后期促进复合物或细胞周期体(APC/C)是一种泛素连接酶,它控制细胞有丝分裂进程以及细胞周期的G1期。APC/C是一个1.5兆道尔顿的复合物,由至少12种不同的核心亚基组成。在有丝分裂和G1期的不同阶段,APC/C与多种调节蛋白结合,如激活蛋白Cdc20和Cdh1以及有丝分裂检查点复合物(MCC),它们以底物特异性的方式调节APC/C的活性。尽管对APC/C及其调节因子进行了深入研究,但对于APC/C如何识别底物并使其泛素化、这些过程为何需要如此多的亚基以及APC/C的调节因子如何以底物特异性的方式控制其泛素连接酶活性,人们仍然知之甚少。本章介绍了一种简单快速的方法,可从脊椎动物细胞和组织中以合理的纯度和高浓度分离出APC/C,产量可达0.5毫克的APC/C。该方法应有助于对APC/C进行生化、生物物理和结构分析,从而更好地从机制上理解其功能和调节。