Shi G, Crivellone M D, Edderkaoui B
Molecular Biology Department, University of Medicine and Dentistry of New Jersey, School of Osteopathic Medicine, Stratford, NJ 08084, USA.
Biochim Biophys Acta. 2001 Aug 17;1506(2):103-16. doi: 10.1016/s0005-2728(01)00187-6.
The Cbp3 protein of Saccharomyces cerevisiae is an enzyme-specific chaperone required for the assembly of ubiquinol-cytochrome c reductase of the mitochondrial respiratory chain. To gain preliminary insight into the role of Cbp3p during assembly, 29 independently isolated mutants were examined to define functional regions of the protein. Mutants were analyzed with respect to respiratory growth, ubiquinol-cytochrome c reductase assembly, and steady state amounts of enzyme subunits and Cbp3p. Three regions essential for Cbp3p activity were identified: regions 1 and 3 were required for Cbp3p function, while region 2 was necessary for protein stability. Mutation of Glu134 in region 1 (Cys124 through Ala140) impaired the ability of the Rieske FeS protein to assemble with the enzyme complex. Mutations targeted to region 3 (Gly223 through Asp229) primarily affected the 14 kDa subunit and cytochrome c(1) assembly. Gly223 was found especially sensitive to mutation and the introduction of charged residues at this site compromised Cbp3p functional activity. Region 2 (Leu167 through Pro175) overlapped the single hydrophobic domain of Cbp3p. Mutations within this area altered the association of Cbp3p with the mitochondrial membrane resulting in enhanced protein turnover. The role of the amino-terminus in Cbp3p activity was investigated using cbp3 deletion strains Delta12-23, Delta24-54, Delta56-96 and Delta12-96. All mutants were respiratory competent, indicating that residues 12-96 were not essential for Cbp3p function, stability or mitochondrial import. Analysis of carboxy-terminal deletion mutants demonstrated that the final 44 residues were not necessary for Cbp3p function; however, alterations in the secondary structure of the extreme carboxy-terminal 17 residues affected assembly protein activity.
酿酒酵母的Cbp3蛋白是线粒体呼吸链泛醇 - 细胞色素c还原酶组装所需的一种酶特异性伴侣蛋白。为了初步了解Cbp3p在组装过程中的作用,研究人员检测了29个独立分离的突变体,以确定该蛋白的功能区域。对突变体进行了呼吸生长、泛醇 - 细胞色素c还原酶组装以及酶亚基和Cbp3p稳态量方面的分析。确定了Cbp3p活性所必需的三个区域:区域1和区域3是Cbp3p功能所必需的,而区域2是蛋白质稳定性所必需的。区域1(Cys124至Ala140)中的Glu134突变削弱了 Rieske FeS 蛋白与酶复合物组装的能力。靶向区域3(Gly223至Asp229)的突变主要影响14 kDa亚基和细胞色素c(1)的组装。发现Gly223对突变特别敏感,在此位点引入带电残基会损害Cbp3p的功能活性。区域2(Leu167至Pro175)与Cbp3p的单个疏水结构域重叠。该区域内的突变改变了Cbp3p与线粒体膜的结合,导致蛋白质周转加快。使用cbp3缺失菌株Delta12 - 23、Delta24 - 54、Delta56 - 96和Delta12 - 96研究了Cbp3p活性中氨基末端的作用。所有突变体都具有呼吸能力,表明残基12 - 96对Cbp3p的功能、稳定性或线粒体导入不是必需的。对羧基末端缺失突变体的分析表明,最后44个残基对Cbp3p功能不是必需的;然而,极端羧基末端17个残基的二级结构改变会影响组装蛋白的活性。