World Scientific
Skip main navigation

Cookies Notification

We use cookies on this site to enhance your user experience. By continuing to browse the site, you consent to the use of our cookies. Learn More
×

System Upgrade on Tue, May 28th, 2024 at 2am (EDT)

Existing users will be able to log into the site and access content. However, E-commerce and registration of new users may not be available for up to 12 hours.
For online purchase, please visit us again. Contact us at customercare@wspc.com for any enquiries.

ENERGY TRANSDUCTION IN MOLECULAR MACHINES

    https://doi.org/10.1142/S1793292007000635Cited by:1 (Source: Crossref)

    An applied force may cause the conformation and thus, the activity of a biological molecule to change. Here we consider a system in which an oscillating or fluctuating electric field is used to actuate membrane protein activities. Most proteins have electric dipoles and net charges in the structure and their conformations are susceptible to the electric and magnetic perturbation. The shape of a cell may also amplify an electric field across its plasma membrane. Therefore, a membrane integral protein such as an ion channel, an ion pump, or a molecular motor, is especially amenable to electric perturbation. The theory of electroconformational coupling addresses the functional implication of this field effect. When an alternating electric field or a fluctuating electric field is employed to actuate a two-state protein oscillator, the dynamics of the conformational change of the protein can be synchronized with the applied field. Through this two-state protein oscillator, we construct a four-state catalytic wheel by coupling an energy transducer mechanism to the two-state protein oscillator. Analysis shows that the catalytic wheel can extract energy from a disordered external energy source, be it electrical, mechanical, or chemical, and convert this stochastic energy source to a usable energy format. The catalytic wheel is tested with the experimental data on the electric field-stimulated cation pumping of Na, K-ATPase. A dipole ratchet model based on the electroconformational coupling concept will also be discussed and compared with the ATP-dependent rotation of a rotary motor F1-ATPase. Since the working principle of this model is simpler than that of F1-ATPase, it provides an easier way to realize a nanoscale rotary motor than artificially reconstructing a F1-ATPase.