Kahlhöfer Flora, Gansen Max, Zickermann Volker
Structural Bioenergetics Group, Institute of Biochemistry II, Medical School, Goethe University Frankfurt, Max-von-Laue Str. 9, D-60438 Frankfurt, Germany.
Centre for Biomolecular Magnetic Resonance, Institute for Biophysical Chemistry, Goethe University Frankfurt, Max-von-Laue-Str. 9, D-60438 Frankfurt, Germany.
Life (Basel). 2021 May 19;11(5):455. doi: 10.3390/life11050455.
ubiquinone-oxidoreductase (complex I) is the largest membrane protein complex of the respiratory chain. Complex I couples electron transfer to vectorial proton translocation across the inner mitochondrial membrane. The L shaped structure of complex I is divided into a membrane arm and a matrix arm. Fourteen central subunits are conserved throughout species, while some 30 accessory subunits are typically found in eukaryotes. Complex I dysfunction is associated with mutations in the nuclear and mitochondrial genome, resulting in a broad spectrum of neuromuscular and neurodegenerative diseases. Accessory subunit NDUFS4 in the matrix arm is a hot spot for mutations causing Leigh or Leigh-like syndrome. In this review, we focus on accessory subunits of the matrix arm and discuss recent reports on the function of accessory subunit NDUFS4 and its interplay with NDUFS6, NDUFA12, and assembly factor NDUFAF2 in complex I assembly.
泛醌氧化还原酶(复合体I)是呼吸链中最大的膜蛋白复合体。复合体I将电子传递与质子跨线粒体内膜的向量转运偶联起来。复合体I的L形结构分为膜臂和基质臂。14个核心亚基在所有物种中都是保守的,而在真核生物中通常发现约30个辅助亚基。复合体I功能障碍与核基因组和线粒体基因组中的突变有关,导致广泛的神经肌肉和神经退行性疾病。基质臂中的辅助亚基NDUFS4是导致Leigh或Leigh样综合征的突变热点。在本综述中,我们聚焦于基质臂的辅助亚基,并讨论关于辅助亚基NDUFS4的功能及其在复合体I组装中与NDUFS6、NDUFA12和组装因子NDUFAF2相互作用的最新报道。