Protein machines often exhibit long-range interplay between different sites in order to achieve their biological tasks. We investigate and characterize the nonlinear energy localization and the basic mechanisms of energy transfer in protein devices. By studying two different model protein machines, with different biological functions, we show that genuinely nonlinear phenomena are responsible for energy transport between the different machine sites involved in the biological functions. The energy transfer turns out to be extremely efficient from an energetic point of view: by changing the energy initially provided to the model device, we identify a well defined range of energies where the time for the energy transport to occur is minimal and the amount of transferred energy is a maximum. Furthermore, by introducing an implicit solvent, we show that the energy is localized on the internal residues of the protein structure, thus minimizing the dissipation.

Energy transfer in molecular devices / Caraglio, M; Imparato, A. - In: PHYSICAL REVIEW E, STATISTICAL, NONLINEAR, AND SOFT MATTER PHYSICS. - ISSN 1539-3755. - 90:6(2014), p. 062712. [10.1103/PhysRevE.90.062712]

Energy transfer in molecular devices

Imparato, A
2014-01-01

Abstract

Protein machines often exhibit long-range interplay between different sites in order to achieve their biological tasks. We investigate and characterize the nonlinear energy localization and the basic mechanisms of energy transfer in protein devices. By studying two different model protein machines, with different biological functions, we show that genuinely nonlinear phenomena are responsible for energy transport between the different machine sites involved in the biological functions. The energy transfer turns out to be extremely efficient from an energetic point of view: by changing the energy initially provided to the model device, we identify a well defined range of energies where the time for the energy transport to occur is minimal and the amount of transferred energy is a maximum. Furthermore, by introducing an implicit solvent, we show that the energy is localized on the internal residues of the protein structure, thus minimizing the dissipation.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3088197
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