Namslauer Ida, Lee Hyun Ju, Gennis Robert B, Brzezinski Peter
Department of Biochemistry and Biophysics, The Arrhenius Laboratories for Natural Sciences, Stockholm University, Stockholm, Sweden.
Biochim Biophys Acta. 2010 May;1797(5):550-6. doi: 10.1016/j.bbabio.2010.01.027. Epub 2010 Feb 1.
In this work we have investigated the effect of a pathogenic mitochondrial DNA mutation found in human colon cells, at a functional-molecular level. The mutation results in the amino-acid substitution Tyr19His in subunit I of the human CytcO and it is associated with respiratory deficiency. It was introduced into Rhodobacter sphaeroides, which carries a cytochrome c oxidase (cytochrome aa(3)) that serves as a model of the mitochondrial counterpart. The residue is situated in the middle of a pathway that is used to transfer substrate protons as well as protons that are pumped across the membrane. The Tyr33His (equivalent residue in the bacterial CytcO) structural variant of the enzyme was purified and its function was investigated. The results show that in the structurally altered CytcO the activity decreased due to slowed proton transfer; proton transfer from an internal proton donor, the highly-conserved Glu286, to the catalytic site was slowed by a factor of approximately 5, while reprotonation of the Glu from solution was slowed by a factor of approximately 40. In addition, in the structural variant proton pumping was completely impaired. These results are explained in terms of introduction of a barrier for proton transfer through the D pathway and changes in the coordination of water molecules surrounding the Glu286 residue. The study offers an explanation, at the molecular level, to the link between a specific amino-acid substitution and a pathogenic phenotype identified in human colon cells.
在这项工作中,我们在功能分子水平上研究了人类结肠细胞中发现的一种致病性线粒体DNA突变的影响。该突变导致人类细胞色素c氧化酶(CytcO)亚基I中的氨基酸替换Tyr19His,并且与呼吸缺陷有关。它被引入到球形红杆菌中,该菌携带一种细胞色素c氧化酶(细胞色素aa(3)),可作为线粒体对应物的模型。该残基位于用于转移底物质子以及跨膜泵送质子的途径中间。对该酶的Tyr33His(细菌CytcO中的等效残基)结构变体进行了纯化并研究了其功能。结果表明,在结构改变的CytcO中,由于质子转移减慢,活性降低;从内部质子供体、高度保守的Glu286到催化位点的质子转移减慢了约5倍,而溶液中Glu的再质子化减慢了约40倍。此外,在结构变体中质子泵送完全受损。这些结果可以通过引入质子通过D途径转移的障碍以及围绕Glu286残基的水分子配位变化来解释。该研究在分子水平上解释了特定氨基酸替换与在人类结肠细胞中鉴定出的致病表型之间的联系。