• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Semiquinone intermediates are involved in the energy coupling mechanism of E. coli complex I.半醌中间体参与大肠杆菌复合体I的能量偶联机制。
Biochim Biophys Acta. 2015 Aug;1847(8):681-9. doi: 10.1016/j.bbabio.2015.04.004. Epub 2015 Apr 11.
2
Roles of semiquinone species in proton pumping mechanism by complex I.半醌类物质在复合体I质子泵浦机制中的作用。
J Bioenerg Biomembr. 2014 Aug;46(4):269-77. doi: 10.1007/s10863-014-9557-9. Epub 2014 Jul 31.
3
Characterization of the delta muH+-sensitive ubisemiquinone species (SQ(Nf)) and the interaction with cluster N2: new insight into the energy-coupled electron transfer in complex I.δμH⁺敏感的半醌类物质(SQ(Nf))的表征及其与N2簇的相互作用:对复合物I中能量耦合电子转移的新见解。
Biochemistry. 2005 Feb 8;44(5):1744-54. doi: 10.1021/bi048132i.
4
Spin labeling of the Escherichia coli NADH ubiquinone oxidoreductase (complex I).大肠杆菌NADH泛醌氧化还原酶(复合体I)的自旋标记
Biochim Biophys Acta. 2010 Dec;1797(12):1894-900. doi: 10.1016/j.bbabio.2010.10.013. Epub 2010 Oct 16.
5
EPR characterization of ubisemiquinones and iron-sulfur cluster N2, central components of the energy coupling in the NADH-ubiquinone oxidoreductase (complex I) in situ.原位对泛半醌和铁硫簇N2进行电子顺磁共振表征,它们是NADH-泛醌氧化还原酶(复合体I)中能量耦合的核心组分。
J Bioenerg Biomembr. 2002 Jun;34(3):193-208. doi: 10.1023/a:1016083419979.
6
Semiquinone and cluster N6 signals in His-tagged proton-translocating NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli.His 标签的质子移位 NADH:泛醌氧化还原酶(复合物 I)的半醌和簇 N6 信号来自大肠杆菌。
J Biol Chem. 2013 May 17;288(20):14310-14319. doi: 10.1074/jbc.M113.467803. Epub 2013 Mar 29.
7
Roles of subunit NuoL in the proton pumping coupling mechanism of NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli.亚基NuoL在大肠杆菌NADH:泛醌氧化还原酶(复合体I)质子泵浦偶联机制中的作用
J Biochem. 2016 Oct;160(4):205-215. doi: 10.1093/jb/mvw027. Epub 2016 Apr 26.
8
Thermodynamic and EPR studies of slowly relaxing ubisemiquinone species in the isolated bovine heart complex I.对分离出的牛心复合体I中缓慢弛豫的泛半醌物种的热力学和电子顺磁共振研究。
FEBS Lett. 2005 Jan 17;579(2):500-6. doi: 10.1016/j.febslet.2004.11.107.
9
Asp563 of the horizontal helix of subunit NuoL is involved in proton translocation by the respiratory complex I.亚单位 NuoL 水平螺旋的 Asp563 参与呼吸复合物 I 的质子转移。
FEBS Lett. 2012 Mar 23;586(6):699-704. doi: 10.1016/j.febslet.2012.01.056. Epub 2012 Feb 3.
10
The location of NuoL and NuoM subunits in the membrane domain of the Escherichia coli complex I: implications for the mechanism of proton pumping.诺尔(NuoL)和诺姆(NuoM)亚基在大肠杆菌复合体I膜结构域中的定位:对质子泵浦机制的启示
J Biol Chem. 2003 Oct 31;278(44):43114-20. doi: 10.1074/jbc.M308247200. Epub 2003 Aug 15.

引用本文的文献

1
The -Strained EPR Line Shape of Transition-Ion Complexes and Metalloproteins: Four Decades of Misunderstanding and Its Consequences.过渡离子配合物和金属蛋白的应变电子顺磁共振线形:四十年的误解及其后果
Molecules. 2025 Aug 6;30(15):3299. doi: 10.3390/molecules30153299.
2
Proton-Translocating NADH-Ubiquinone Oxidoreductase: Interaction with Artificial Electron Acceptors, Inhibitors, and Potential Medicines.质子转运型NADH-泛醌氧化还原酶:与人工电子受体、抑制剂及潜在药物的相互作用
Int J Mol Sci. 2024 Dec 14;25(24):13421. doi: 10.3390/ijms252413421.
3
Understanding coenzyme Q.了解辅酶 Q.
Physiol Rev. 2024 Oct 1;104(4):1533-1610. doi: 10.1152/physrev.00040.2023. Epub 2024 May 9.
4
Using a chimeric respiratory chain and EPR spectroscopy to determine the origin of semiquinone species previously assigned to mitochondrial complex I.利用嵌合呼吸链和电子顺磁共振波谱技术确定先前分配给线粒体复合物 I 的半醌物种的起源。
BMC Biol. 2020 May 20;18(1):54. doi: 10.1186/s12915-020-00768-6.
5
Redox-coupled quinone dynamics in the respiratory complex I.氧化还原偶联的醌在呼吸复合物 I 中的动态。
Proc Natl Acad Sci U S A. 2018 Sep 4;115(36):E8413-E8420. doi: 10.1073/pnas.1805468115. Epub 2018 Aug 17.
6
Distinct properties of semiquinone species detected at the ubiquinol oxidation Qo site of cytochrome bc1 and their mechanistic implications.在细胞色素bc1的泛醇氧化Qo位点检测到的半醌物种的独特性质及其机制意义。
J R Soc Interface. 2016 May;13(118). doi: 10.1098/rsif.2016.0133.
7
Energy conversion, redox catalysis and generation of reactive oxygen species by respiratory complex I.呼吸链复合体I的能量转换、氧化还原催化及活性氧生成
Biochim Biophys Acta. 2016 Jul;1857(7):872-83. doi: 10.1016/j.bbabio.2015.12.009. Epub 2015 Dec 22.
8
Roles of semiquinone species in proton pumping mechanism by complex I.半醌类物质在复合体I质子泵浦机制中的作用。
J Bioenerg Biomembr. 2014 Aug;46(4):269-77. doi: 10.1007/s10863-014-9557-9. Epub 2014 Jul 31.

本文引用的文献

1
Architecture of mammalian respiratory complex I.哺乳动物呼吸复合体I的结构
Nature. 2014 Nov 6;515(7525):80-84. doi: 10.1038/nature13686. Epub 2014 Sep 7.
2
Energy transducing roles of antiporter-like subunits in Escherichia coli NDH-1 with main focus on subunit NuoN (ND2).大肠杆菌 NDH-1 中类似转运蛋白亚基的能量转导作用,主要关注亚基 nuoN(ND2)。
J Biol Chem. 2013 Aug 23;288(34):24705-16. doi: 10.1074/jbc.M113.482968. Epub 2013 Jul 17.
3
Semiquinone and cluster N6 signals in His-tagged proton-translocating NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli.His 标签的质子移位 NADH:泛醌氧化还原酶(复合物 I)的半醌和簇 N6 信号来自大肠杆菌。
J Biol Chem. 2013 May 17;288(20):14310-14319. doi: 10.1074/jbc.M113.467803. Epub 2013 Mar 29.
4
Mitochondrial complex I.线粒体复合物 I
Annu Rev Biochem. 2013;82:551-75. doi: 10.1146/annurev-biochem-070511-103700. Epub 2013 Mar 18.
5
Crystal structure of the entire respiratory complex I.呼吸复合物 I 的整体晶体结构。
Nature. 2013 Feb 28;494(7438):443-8. doi: 10.1038/nature11871. Epub 2013 Feb 17.
6
EPR detection of two protein-associated ubiquinone components (SQ(Nf) and SQ(Ns)) in the membrane in situ and in proteoliposomes of isolated bovine heart complex I.在分离的牛心复合体I的膜原位和蛋白脂质体中对两种与蛋白质相关的泛醌成分(SQ(Nf)和SQ(Ns))进行电子顺磁共振检测。
Biochim Biophys Acta. 2012 Oct;1817(10):1803-9. doi: 10.1016/j.bbabio.2012.03.032. Epub 2012 Apr 5.
7
Fenpyroximate binds to the interface between PSST and 49 kDa subunits in mitochondrial NADH-ubiquinone oxidoreductase.芬普洛司特与线粒体 NADH-泛醌氧化还原酶 PSST 和 49 kDa 亚基之间的界面结合。
Biochemistry. 2012 Mar 6;51(9):1953-63. doi: 10.1021/bi300047h. Epub 2012 Feb 27.
8
A two-state stabilization-change mechanism for proton-pumping complex I.质子泵复合物I的双态稳定-变化机制。
Biochim Biophys Acta. 2011 Oct;1807(10):1364-9. doi: 10.1016/j.bbabio.2011.04.006. Epub 2011 May 2.
9
Evolution of respiratory complex I: "supernumerary" subunits are present in the alpha-proteobacterial enzyme.呼吸复合物 I 的进化:“多余”的亚基存在于α-变形菌的酶中。
J Biol Chem. 2011 Feb 18;286(7):5023-33. doi: 10.1074/jbc.M110.194993. Epub 2010 Nov 29.
10
The membrane subunit NuoL(ND5) is involved in the indirect proton pumping mechanism of Escherichia coli complex I.膜亚基 NuoL(ND5)参与大肠杆菌复合体 I 的间接质子泵机制。
J Biol Chem. 2010 Dec 10;285(50):39070-8. doi: 10.1074/jbc.M110.157826. Epub 2010 Sep 7.

半醌中间体参与大肠杆菌复合体I的能量偶联机制。

Semiquinone intermediates are involved in the energy coupling mechanism of E. coli complex I.

作者信息

Narayanan Madhavan, Leung Steven A, Inaba Yuta, Elguindy Mahmoud M, Nakamaru-Ogiso Eiko

机构信息

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.

出版信息

Biochim Biophys Acta. 2015 Aug;1847(8):681-9. doi: 10.1016/j.bbabio.2015.04.004. Epub 2015 Apr 11.

DOI:10.1016/j.bbabio.2015.04.004
PMID:25868873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4458183/
Abstract

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.

摘要

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。