Acidic lipids, H +-ATPases, and mechanism of oxidative phosphorylation. Physico-chemical ideas 30 years after P. Mitchell's Nobel Prize award

Peter D. Mitchell, who was awarded the Nobel Prize in Chemistry 30 years ago, in 1978, formulated the chemiosmotic theory of oxidative phosphorylation. This review initially analyzes the major aspects of this theory, its unresolved problems, and its modifications. A new physico-chemical mechanism of...

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Bibliographic Details
Published in:Progress in biophysics and molecular biology 2009, Vol.99 (1), p.20-41
Main Author: Kocherginsky, Nikolai
Format: Article
Language:English
Subjects:
Acids
ATPase
Bioenergetics
Cardiolipin
Enzyme Activation
Lipids - chemistry
Membrane
Mitochondria
Models, Chemical
Models, Molecular
Molecular motor
Nobel Prize
Oxidation-Reduction
Oxidative phosphorylation
Phosphorylation
Proton-Translocating ATPases - chemistry
Proton-Translocating ATPases - ultrastructure
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Summary:Peter D. Mitchell, who was awarded the Nobel Prize in Chemistry 30 years ago, in 1978, formulated the chemiosmotic theory of oxidative phosphorylation. This review initially analyzes the major aspects of this theory, its unresolved problems, and its modifications. A new physico-chemical mechanism of energy transformation and coupling of oxidation and phosphorylation is then suggested based on recent concepts regarding proteins, including ATPases that work as molecular motors, and acidic lipids that act as hydrogen ion (H +) carriers. According to this proposed mechanism, the chemical energy of a redox substrate is transformed into nonequilibrium states of electron-transporting chain (ETC) coupling proteins. This leads to nonequilibrium pumping of H + into the membrane. An acidic lipid, cardiolipin, binds with this H + and carries it to the ATP-synthase along the membrane surface. This transport generates gradients of surface tension or electric field along the membrane surface. Hydrodynamic effects on a nanolevel lead to rotation of ATP-synthase and finally to the release of ATP into aqueous solution. This model also explains the generation of a transmembrane protonmotive force that is used for regulation of transmembrane transport, but is not necessary for the coupling of electron transport and ATP synthesis.
ISSN:0079-6107
1873-1732
DOI:10.1016/j.pbiomolbio.2008.10.013