van Dijl J M, Kutejová E, Suda K, Perecko D, Schatz G, Suzuki C K
Department of Pharmaceutical Biology, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.
Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10584-9. doi: 10.1073/pnas.95.18.10584.
The ATP-dependent Lon protease of Saccharomyces cerevisiae mitochondria is required for selective proteolysis in the matrix, maintenance of mitochondrial DNA, and respiration-dependent growth. Lon may also possess a chaperone-like function that facilitates protein degradation and protein-complex assembly. To understand the influence of Lon's ATPase and protease activities on these functions, we examined several Lon mutants for their ability to complement defects of Lon-deleted yeast cells. We also developed a rapid procedure for purifying yeast Lon to homogeneity to study the enzyme's activities and oligomeric state. A point mutation in either the ATPase or the protease site strongly inhibited the corresponding activity of the pure protein but did not alter the protein's oligomerization; when expressed at normal low levels neither of these mutant enzymes supported respiration-dependent growth of Lon-deleted cells. When the ATPase- or the protease-containing regions of Lon were expressed as separate truncated proteins, neither could support respiration-dependent growth of Lon-deleted cells; however, coexpression of these two separated regions sustained wild-type growth. These results suggest that yeast Lon contains two catalytic domains that can interact with one another even as separate proteins, and that both are essential for the different functions of Lon.
酿酒酵母线粒体中依赖ATP的Lon蛋白酶是线粒体基质中选择性蛋白水解、线粒体DNA维持以及呼吸依赖性生长所必需的。Lon可能还具有类似伴侣蛋白的功能,有助于蛋白质降解和蛋白质复合物组装。为了了解Lon的ATP酶和蛋白酶活性对这些功能的影响,我们检测了几种Lon突变体互补Lon缺失酵母细胞缺陷的能力。我们还开发了一种快速方法,可将酵母Lon纯化至同质,以研究该酶的活性和寡聚状态。ATP酶位点或蛋白酶位点的点突变强烈抑制了纯蛋白的相应活性,但未改变蛋白的寡聚化;当以正常低水平表达时,这两种突变酶均不能支持Lon缺失细胞的呼吸依赖性生长。当Lon的含ATP酶或蛋白酶区域作为单独的截短蛋白表达时,两者均不能支持Lon缺失细胞的呼吸依赖性生长;然而,这两个分离区域的共表达维持了野生型生长。这些结果表明,酵母Lon含有两个催化结构域,即使作为单独的蛋白质也能相互作用,并且两者对于Lon的不同功能都是必不可少的。