A protet-based model that can account for energy coupling in oxidative and photosynthetic phosphorylation

被引:0
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作者
Kell, Douglas B. [1 ,2 ,3 ]
机构
[1] Univ Liverpool, Inst Syst Mol & Integrat Biol, Fac Hlth & Life Sci, Dept Biochem Cell & Syst Biol, Liverpool L69 7ZB, England
[2] Tech Univ Denmark, Novo Nordisk Fdn Ctr Biosustainabil, Bldg 220, DK-2800 Lyngby, Denmark
[3] Stellenbosch Univ, Fac Sci, Dept Physiol Sci, Private Bag X1, ZA-7602 Matieland, South Africa
来源
关键词
Protet; Localised coupling; OXPHOS; Photosynthetic phosphorylation; POST-ILLUMINATION PHOSPHORYLATION; UNCOUPLER-BINDING PROTEIN; SINGLE-TURNOVER FLASHES; FORMATION ONSET LAG; MITOCHONDRIAL-MEMBRANE; GIANT MITOCHONDRIA; ATP FORMATION; ELECTRICAL-PROPERTIES; BIOLOGICAL-MEMBRANES; MECHANISM;
D O I
10.1016/j.bbabio.2024.149504
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
Two-stage (e.g. light-dark) phosphorylation experiments showed that there is a stored 'high-energy' intermediate linking electron transport and phosphorylation. Large, artificial electrochemical proton gradients (protonmotive forces or pmfs) can also drive phosphorylation, a fact seen as strongly supportive of the chemiosmotic coupling hypothesis that a pmf is the 'high-energy' intermediate. However, in such experiments there is an experimental threshold (pmf >170 mV, equivalent to Delta pH similar to 2.8) below which no phosphorylation is in fact observed, and 220 mV are required to recreate in vivo rates. This leads to the correct question, which is then whether those values of the pmf generated by electron transport are large enough. Even the lower ones as required for any phosphorylation (leave alone those required to explain in vivo rates) are below the threshold [1, 2], whether measured directly with microelectrodes or via the use of membrane-permeant ions and/or acids/bases (which are always transporter substrates [3], so all such measurements are in fact artefactual). The single case that seemed large enough (220 mV) is now admitted to be a diffusion potential artefact [4]. Many other observables (inadequate bulk H+ in 'O-2-pulse'-type experiments, alkaliphilic bacteria, dual-inhibitor titrations, uncoupler-binding proteins, etc.) are consistent with the view that values of the pmf, and especially of Delta psi, are actually very low. A protet-based charge separation model [2], a protonic version analogous to how energy may be stored in devices called electrets, provides a high-energy intermediate that can explain the entire literature, including the very striking demonstration [5] that close proximity is required between electron transport and ATP synthase complexes for energy coupling between them to allow phosphorylation to occur. A chief purpose of this article is thus to summarise the extensive and self-consistent literature, much of which is of some antiquity and rarely considered by modern researchers, despite its clear message of the inadequacy of chemiosmotic coupling to explain these phenomena.
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