Distribution and dynamics of quinones in the lipid bilayer mimicking the inner membrane of mitochondria

被引:34
|
作者
Kaurola, Petri [1 ]
Sharma, Vivek [1 ,2 ]
Vonk, Amanda [1 ]
Vattulainen, Ilpo [1 ,2 ,3 ]
Rog, Tomasz [1 ,2 ]
机构
[1] Tampere Univ Technol, Dept Phys, POB 692, FI-33101 Tampere, Finland
[2] Univ Helsinki, Dept Phys, POB 64, FI-00014 Helsinki, Finland
[3] Univ Southern Denmark, MEMPHYS Ctr Biomembrane Phys, DK-5230 Odense M, Denmark
来源
基金
欧洲研究理事会; 芬兰科学院;
关键词
Electron transport chain; Molecular dynamics simulations; Free energy calculations; Biological energy transduction; AA FORCE-FIELD; MOLECULAR-DYNAMICS; COENZYME-Q; CRYSTAL-STRUCTURE; SIMULATIONS; UBIQUINONE; BIOSYNTHESIS; CHOLESTEROL; TOPOLOGIES; PROTEINS;
D O I
10.1016/j.bbamem.2016.06.016
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
Quinone and its analogues (Q) constitute an important class of compounds that perform key electron transfer reactions in oxidative- and photo-phosphorylation. In the inner membrane of mitochondria, ubiquinone molecules undergo continuous redox transitions enabling electron transfer between the respiratory complexes. In such a dynamic system undergoing continuous turnover for ATP synthesis, an uninterrupted supply of substrate molecules is absolutely necessary. In the current work, we have performed atomistic molecular dynamics simulations and free energy calculations to assess the structure, dynamics, and localization of quinone and its analogues in a lipid bilayer, whose composition mimics the one in the inner mitochondrial membrane. The results show that there is a strong tendency of both quinone and quinol molecules to localize in the vicinity of the lipids' acyl groups, right under the lipid head group region. Additionally, we observe a second location in the middle of the bilayer where quinone molecules tend to stabilize. Translocation of quinone through a lipid bilayer is very fast and occurs in 10-100 ns time scale, whereas the translocation of quinol is at least an order of magnitude slower. We suggest that this has important mechanistic implications given that the localization of Q ensures maximal occupancy of the Q-binding sites or Q-entry points in electron transport chain complexes, thereby maintaining an optimal turnover rate for ATP synthesis. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:2116 / 2122
页数:7
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