Thermodynamic and EPR studies of slowly relaxing ubisemiquinone species in the isolated bovine heart complex I

被引:58
作者
Ohnishi, T [1 ]
Johnson, JE
Yano, T
LoBrutto, R
Widger, WR
机构
[1] Univ Penn, Dept Biochem & Biophys, Johnson Res Fdn, Philadelphia, PA 19104 USA
[2] Univ Houston, Dept Biol & Biochem, Houston, TX 77204 USA
[3] Arizona State Univ, Sch Life Sci, LSE 218, Tempe, AZ 85287 USA
来源
FEBS LETTERS | 2005年 / 579卷 / 02期
关键词
NADH : ubiquinone oxidoreductase; ubisemiquinone; EPR spectrum; E-m;
D O I
10.1016/j.febslet.2004.11.107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previously, we investigated ubisemiquinone (SQ) EPR spectra associated with NADH-ubiquinone oxidoreductase (complex 1) in the tightly coupled bovine heart submitochondrial particles (SMP). Based upon their widely differing spin relaxation rate, we distinguished SQ spectra arising from three distinct SQ species, namely SQ(Nf) (fast), SQ(Ns) (slow), and SQ(Nx) (very slow). The SQNf signal was observed only in the presence of the proton electrochemical gradient (Deltamu(H)(+)), while SQ(Ns) and SQ(Nx) species did not require the presence of Deltamu(H)(+). We have now succeeded in characterizing the redox and EPR properties of SQ species in the isolated bovine heart complex 1. The potentiometric redox titration of the g(z,y,x) = 2.00 semiquinone signal gave the redox midpoint potential (E-m) at pH 7.8 for the first electron transfer step [E-m1(Q/SQ)] of -45 mV and the second step [E-m2(SQ/QH(2))] of -63 mV. It can also be expressed as [E-m(Q/QH(2))] of -54 mV for the overall two electron transfer with a stability constant (K-stab) of the SQ form as 2.0. These characteristics revealed the existence of a thermodynamically stable intermediate redox state, which allows this protein-associated quinone to function as a converter between n = 1 and n = 2 electron transfer steps. The EPR spectrum of the SQ species in complex I exhibits a Gaussian-type spectrum with the peak-to-peak line width of similar to6.1 G at the sample temperature of 173 K. This indicates that the SQ species is in an anionic Q(.-) state in the physiological pH range. The spin relaxation rate of the SQ species in isolated complex I is much slower than the SQ counterparts in the complex I in situ in SMP. We tentatively assigned slow relaxing anionic SQ species as SQ(Ns), based on the monophasic power saturation profile and several fold increase of its spin relaxation rate in the presence of reduced cluster N2. The current study also suggests that the very slowly relaxing SQ(Nx). species may not be an intrinsic complex I component. The functional role of SQ(Ns) is further discussed in connection with the SQ(Nf) species defined in SMP in situ. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:500 / 506
页数:7
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