Narayanan Madhavan, Leung Steven A, Inaba Yuta, Elguindy Mahmoud M, Nakamaru-Ogiso Eiko
Johnson Research Foundation, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Johnson Research Foundation, Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Biochim Biophys Acta. 2015 Aug;1847(8):681-9. doi: 10.1016/j.bbabio.2015.04.004. Epub 2015 Apr 11.
Complex I (NADH:quinone oxidoreductase) is central to cellular aerobic energy metabolism, and its deficiency is involved in many human mitochondrial diseases. Complex I translocates protons across the membrane using electron transfer energy. Semiquinone (SQ) intermediates appearing during catalysis are suggested to be key for the coupling mechanism in complex I. However, the existence of SQ has remained controversial due to the extreme difficulty in detecting unstable and low intensity SQ signals. Here, for the first time with Escherichia coli complex I reconstituted in proteoliposomes, we successfully resolved and characterized three distinct SQ species by EPR. These species include: fast-relaxing SQ (SQNf) with P1/2 (half-saturation power level)>50mW and a wider linewidth (12.8 G); slow-relaxing SQ (SQNs) with P1/2=2-3mW and a 10G linewidth; and very slow-relaxing SQ (SQNvs) with P1/2= ~0.1mW and a 7.5G linewidth. The SQNf signals completely disappeared in the presence of the uncoupler gramicidin D or squamotacin, a potent E. coli complex I inhibitor. The pH dependency of the SQNf signals correlated with the proton-pumping activities of complex I. The SQNs signals were insensitive to gramicidin D, but sensitive to squamotacin. The SQNvs signals were insensitive to both gramicidin D and squamotacin. Our deuterium exchange experiments suggested that SQNf is neutral, while SQNs and SQNvs are anion radicals. The SQNs signals were lost in the ΔNuoL mutant missing transporter module subunits NuoL and NuoM. The roles and relationships of the SQ intermediates in the coupling mechanism are discussed.
复合物I(NADH:醌氧化还原酶)是细胞有氧能量代谢的核心,其缺陷与许多人类线粒体疾病有关。复合物I利用电子传递能量将质子跨膜转运。催化过程中出现的半醌(SQ)中间体被认为是复合物I偶联机制的关键。然而,由于检测不稳定且强度低的SQ信号极其困难,SQ的存在一直存在争议。在此,我们首次利用重组在蛋白脂质体中的大肠杆菌复合物I,通过电子顺磁共振(EPR)成功解析并表征了三种不同的SQ物种。这些物种包括:P1/2(半饱和功率水平)>50mW且线宽较宽(12.8 G)的快速弛豫SQ(SQNf);P1/2 = 2 - 3mW且线宽为10G的慢速弛豫SQ(SQNs);以及P1/2 = ~0.1mW且线宽为7.5G的极慢速弛豫SQ(SQNvs)。在解偶联剂短杆菌肽D或强效大肠杆菌复合物I抑制剂鳞霉素存在的情况下,SQNf信号完全消失。SQNf信号的pH依赖性与复合物I的质子泵浦活性相关。SQNs信号对短杆菌肽D不敏感,但对鳞霉素敏感。SQNvs信号对短杆菌肽D和鳞霉素均不敏感。我们的氘交换实验表明,SQNf是中性的,而SQNs和SQNvs是阴离子自由基。在缺失转运体模块亚基NuoL和NuoM的ΔNuoL突变体中,SQNs信号消失。本文讨论了SQ中间体在偶联机制中的作用和关系。