We have trapped single protein molecules of R-phycoerythrin in an aqueous solution by an alternating electric field. A radio frequency voltage is applied to sharp nanoelectrodes and hence produces a strong electric field gradient. The resulting dielectrophoretic forces attract freely diffusing protein molecules. Trapping takes place at the electrode tips. Switching off the field immediately releases the molecules. The electric field distribution is computed, and from this the dielectrophoretic response of the molecules is calculated using a standard polarization model. The resulting forces are compared to the impact of Brownian motion. Finally, we discuss the experimental observations on the basis of the model calculations.

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As it follows from the results of C. H. Waddigton, F. E. Yates, A. S. Iberall, and other well-known bio-physicists, living fluids cannot be modelled within the frames of the fundamental assumptions of the statistical-mechanics formalism. One has to go beyond them. The present work does it by means of the generalized kinetics (GK), the theory enabling one to allow for the complex stochasticity of internal properties and parameters of the fluid particles. This is one of the key features which distinguish living fluids from the nonliving ones. It creates the disparity of the particles and hence breaks the eachfluid-component-uniformity requirement underlying statistical mechanics.The work deals with the corresponding modification of common kinetic equations which is in line with the GK theory and is the complement to the latter. This complement allows a subdivision of a fluid into the fluid components in terms of nondiscrete probability distributions. The treatment leads to one more equation that describes the above internal parameters. The resulting model is the system of these two equations. It appears to be always nonlinear in case of living fluids. In case of nonliving fluids, the model can be linear. Moreover, the living-fluid model, as a whole, cannot have the thermodynamic equilibrium, only partial equilibriums (such as the motional one) are possible. In contrast to this, in case of nonliving fluids, the thermodynamic equilibrium is, of course, possible. The number of the fluid components is treated as the number of the modes of the particle-characteristic probability density. In so doing, a fairly general extension of the notion of the mode from the one-dimensional case to the multidimensional case is proposed. The work also discusses the variety of the time-scales in a living fluid, the simplest quantum-mechanical equation relevant to living fluids, and the nonequilibrium nonlinear stochastic hydrodynamics option. The latter is simpler than, but conceptually comparable to, stochastic kinetic equations. A few directions for future research are suggested. The work notes a cohesion of mathematical physics and fluid mechanics with the living-fluid-related fields as a complex interdisciplinary problem.Keywords: Multicomponent fluid of living cells and related macromolecules; generalized kinetic theory; stochastic differential equation; probability distribution of parameters of the fluid particles; mode of probability distribution and multimodal distributions.

We demonstrate a nanoscale water-based transistor. The presented nanoscale water-based transistor relies on the controlled modification of the pH in deionized water through the base applied electric field. The dc characteristics are presented and studied with a focus on the influence of the base applied electric field, the base electrode design, and their proximity to the sensing emitter and collector nanoelectrodes. The demonstrated water-based nanoscale device is of interest for many bioelectrical applications due to the biocompatibility and the wide usage and presence of water in biological systems.

UV induced negative current produced at low voltages is reported in a photocurrent rectifier device consisting of a sensing region between two nano Al∕Al2O3 electrodes placed 30nm apart, employing a droplet of enhanced green fluorescent protein as molecular electrolyte. The current-voltage characteristics are discussed in terms of the properties of the thin Al2O3 scale, the position of the Fermi level, the position of the highest occupied molecular orbital-lowest unoccupied molecular orbital gap, and dispersion of states induced by varying dielectric constants.