The functional design of the rotary enzyme ATP synthase is consistent with maximum entropy production

R. C. Dewar*, D. Juretić, P. Županović

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

42 Citations (Scopus)

Abstract

We show that the molecular motor ATP synthase has evolved in accordance with the statistical selection principle of Maximum Shannon Entropy and one of its corollaries, Maximum Entropy Production. These principles predict an optimal angular position for the ATP-binding transition close to the experimental value; an inverse relation between the optimal gearing ratio and the proton motive force (pmf); optimal operation at an inflection point in the curve of ATP synthesis rate versus pmf, enabling rapid metabolic control; and a high optimal free energy conversion efficiency. Our results suggest a statistical interpretation for the evolutionary optimization of ATP synthase function.

Original languageEnglish
Pages (from-to)177-182
Number of pages6
JournalChemical Physics Letters
Volume430
Issue number1-3
DOIs
Publication statusPublished - 19 Oct 2006
Externally publishedYes

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