Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0cp02118k
DC FieldValue
dc.titleUniversal optimal working cycles of molecular motors
dc.contributor.authorEfremov, A.
dc.contributor.authorWang, Z.
dc.date.accessioned2014-10-16T09:48:10Z
dc.date.available2014-10-16T09:48:10Z
dc.date.issued2011-04-07
dc.identifier.citationEfremov, A., Wang, Z. (2011-04-07). Universal optimal working cycles of molecular motors. Physical Chemistry Chemical Physics 13 (13) : 6223-6233. ScholarBank@NUS Repository. https://doi.org/10.1039/c0cp02118k
dc.identifier.issn14639076
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/98527
dc.description.abstractMolecular motors capable of directional track-walking or rotation are abundant in living cells, and inspire the emerging field of artificial nanomotors. Some biomotors can convert 90% of free energy from chemical fuels into usable mechanical work, and the same motors still maintain a speed sufficient for cellular functions. This study exposed a new regime of universal optimization that amounts to a thermodynamically best working regime for molecular motors but is unfamiliar in macroscopic engines. For the ideal case of zero energy dissipation, the universally optimized working cycle for molecular motors is infinitely slow like Carnot cycle for heat engines. But when a small amount of energy dissipation reduces energy efficiency linearly from 100%, the speed is recovered exponentially due to Boltzmann's law. Experimental data on a major biomotor (kinesin) suggest that the regime of universal optimization has been largely approached in living cells, underpinning the extreme efficiency-speed trade-off in biomotors. The universal optimization and its practical approachability are unique thermodynamic advantages of molecular systems over macroscopic engines in facilitating motor functions. The findings have important implications for the natural evolution of biomotors as well as the development of artificial counterparts. © the Owner Societies. 2011.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0cp02118k
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.description.doi10.1039/c0cp02118k
dc.description.sourcetitlePhysical Chemistry Chemical Physics
dc.description.volume13
dc.description.issue13
dc.description.page6223-6233
dc.description.codenPPCPF
dc.identifier.isiut000288447100090
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