Wyatt Amy R, Yerbury Justin J, Wilson Mark R
School of Biological Sciences, University of Wollongong, Wollongong, New South Wales 2522, Australia.
J Biol Chem. 2009 Aug 14;284(33):21920-21927. doi: 10.1074/jbc.M109.033688. Epub 2009 Jun 17.
Clusterin (CLU) is a potent extracellular chaperone that inhibits protein aggregation and precipitation otherwise caused by physical or chemical stresses (e.g. heat, reduction). This action involves CLU forming soluble high molecular weight (HMW) complexes with the client protein. Other than their unquantified large size, the physical characteristics of these complexes were previously unknown. In this study, HMW CLU-citrate synthase (CS), HMW CLU-fibrinogen (FGN), and HMW CLU-glutathione S-transferase (GST) complexes were generated in vitro, and their structures studied using size exclusion chromatography (SEC), ELISA, SDS-PAGE, dynamic light scattering (DLS), bisANS fluorescence, and circular dichroism spectrophotometry (CD). Densitometry of Coomassie Blue-stained SDS-PAGE gels indicated that all three HMW CLU-client protein complexes had an approximate mass ratio of 1:2 (CLU:client protein). SEC indicated that all three clients formed complexes with CLU>or=4x10(7) Da; however, DLS estimated HMW CLU-FGN to have a diameter of 108.57+/-18.09 nm, while HMW CLU-CS and HMW CLU-GST were smaller with estimated diameters of 51.06+/-6.87 nm and 52.61+/-7.71 nm, respectively. Measurements of bisANS fluorescence suggest that the chaperone action of CLU involves preventing the exposure to aqueous solvent of hydrophobic regions that are normally exposed by the client protein during heat-induced unfolding. CD analysis indicated that, depending on the individual client protein, CLU may interact with a variety of intermediates on protein unfolding pathways with different amounts of native secondary structure. In vivo, soluble complexes like those studied here are likely to serve as vehicles to dispose of otherwise dangerous aggregation-prone misfolded extracellular proteins.
簇集素(CLU)是一种强大的细胞外伴侣蛋白,可抑制由物理或化学应激(如热、还原)引起的蛋白质聚集和沉淀。这一作用涉及CLU与目标蛋白形成可溶性高分子量(HMW)复合物。除了其大小无法量化外,这些复合物的物理特性此前尚不清楚。在本研究中,体外生成了HMW CLU-柠檬酸合酶(CS)、HMW CLU-纤维蛋白原(FGN)和HMW CLU-谷胱甘肽S-转移酶(GST)复合物,并使用尺寸排阻色谱(SEC)、酶联免疫吸附测定(ELISA)、十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)、动态光散射(DLS)、双-ANS荧光和圆二色光谱法(CD)研究了它们的结构。考马斯亮蓝染色的SDS-PAGE凝胶的光密度测定表明,所有三种HMW CLU-目标蛋白复合物的质量比约为1:2(CLU:目标蛋白)。SEC表明,所有三种目标蛋白均与CLU形成了分子量≥4×10⁷ Da的复合物;然而,DLS估计HMW CLU-FGN的直径为108.57±18.09 nm,而HMW CLU-CS和HMW CLU-GST较小,估计直径分别为51.06±6.87 nm和52.61±7.71 nm。双-ANS荧光测量表明,CLU的伴侣蛋白作用涉及防止目标蛋白在热诱导的解折叠过程中通常暴露的疏水区域暴露于水性溶剂中。CD分析表明,根据单个目标蛋白的不同,CLU可能与蛋白质解折叠途径上具有不同天然二级结构量的各种中间体相互作用。在体内,此处研究的可溶性复合物可能充当载体,以处理原本危险的、易于聚集的错误折叠细胞外蛋白。