4.5 Article

Study of ion translocation by respiratory complex I. A new insight using 23Na NMR spectroscopy

期刊

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
卷 1817, 期 10, 页码 1810-1816

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbabio.2012.03.009

关键词

Complex I; NADH:quinone oxidoreductase; Na-23 NMR spectroscopy; Resonance frequency shift; Shift reagent,Tm(DOTP)(5-)

资金

  1. FCT, Projecto de Re-Equipamento Cientifico [REDE/1517/RMN/2005]
  2. FCT [REEQ/336/BIO/2005]
  3. Fundacao para a Ciencia e a Tecnologia [SFRH/BPD/80741/2011, PTDC/QUI-BIQ/100302/2008, PEst-OE/EQB/LA0004/2011]
  4. Fundação para a Ciência e a Tecnologia [PTDC/QUI-BIQ/100302/2008] Funding Source: FCT

向作者/读者索取更多资源

The research on complex I has gained recently a new enthusiasm, especially after the resolution of the crystallographic structures of bacterial and mitochondrial complexes. Most attention is now dedicated to the investigation of the energy coupling mechanism(s). The proton has been identified as the coupling ion, although in the case of some bacterial complexes I Na+ has been proposed to have that role. We have addressed the relation of some complexes I with Na+ and developed an innovative methodology using Na-23 NMR spectroscopy. This allowed the investigation of Na+ transport taking the advantage of directly monitoring changes in Na+ concentration. Methodological aspects concerning the use of Na-23 NMR spectroscopy to measure accurately sodium transport in bacterial membrane vesicles are discussed here. Externalvesicle Na+ concentrations were determined by two different methods: 1) by integration of the resonance frequency peak and 2) using calibration curves of resonance frequency shift dependence on Na+ concentration. Although the calibration curves are a suitable way to determine Na+ concentration changes under conditions of fast exchange, it was shown not to be applicable to the bacterial membrane vesicle systems. In this case, the integration of the resonance frequency peak is the most appropriate analysis for the quantification of external-vesicle Na+ concentration. This article is part of a Special Issue entitled: 17th European Bioenergetics Conference (EBEC 2012). (C) 2012 Elsevier B.V. All rights reserved.

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