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Riku Kato

Publications and source records attributed to Riku Kato.

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Energy Conversion, Fluctuation Suppression, and Information Transfer in the Thermodynamic Performance of Kinesin

Kinesin is a molecular motor that transports intracellular cargoes along microtubules. Recent studies have quantified kinesin performance using various efficiencies within the framework of stochastic thermodynamics; however, quantitative comparisons remain difficult because different models and assumptions have been employed. As a result, it remains unclear which aspect of kinesin performance, if any, is thermodynamically optimized. Here, we systematically compare multiple thermodynamic efficiencies within a single kinesin-cargo model. To this end, we construct a thermodynamically consistent two-state kinesin-cargo model that retains both the discrete stepping of kinesin and its coupling to the cargo. Assuming a separation of time scales between the motor and the cargo, we derive analytical expressions for the thermodynamic efficiency, the information-thermodynamic efficiency, the thermodynamic uncertainty relation (TUR) efficiency, and the bipartite TUR efficiency, and compare them with numerical simulation results. We find that these efficiencies generally remain low, suggesting that kinesin is not optimized for maximizing the thermodynamic efficiencies considered here. Our results suggest that thermodynamic efficiencies alone may not fully characterize kinesin performance and motivate further investigation of complementary kinetic perspectives for assessing molecular motor function.

cond-mat.stat-mech

Microscopic Characterization of Individual Submicron Bubbles during the Layer-by-Layer Deposition: Towards Creating Smart Agents

We investigated the individual properties of various polyion-coated bubbles with a mean diameter ranging from 300 to 500 nm. Dark field microscopy allows one to track the individual particles of the submicron bubbles (SBs) encapsulated by the layer-by-layer (LbL) deposition of cationic and anionic polyelectrolytes (PEs). Our focus is on the two-step charge reversals of PE-SB complexes: the first is a reversal from negatively charged bare SBs with no PEs added to positive SBs encapsulated by polycations (monolayer deposition), and the second is overcharging into negatively charged PE-SB complexes due to the subsequent addition of polyanions (double-layer deposition). The details of these phenomena have been clarified through the analysis of a number of trajectories of various PE-SB complexes that experience either Brownian motion or electrophoresis. The contrasted results obtained from the analysis were as follows: an amount in excess of the stoichiometric ratio of the cationic polymers was required for the first charge-reversal, whereas the stoichiometric addition of the polyanions lead to the electrical neutralization of the PE-SB complex particles. The recovery of the stoichiometry in the double-layer deposition paves the way for fabricating multi-layered SBs encapsulated solely with anionic and cationic PEs, which provides a simple protocol to create smart agents for either drug delivery or ultrasound contrast imaging.

cond-mat.soft