Ratcheted diffusion transport through crowded nanochannels
Anna Lappala, Alessio Zaccone, Eugene M. Terentjev

TL;DR
This paper investigates the mechanisms of Brownian ratchet-driven transport in nanochannels, identifying regimes of individual and crowded particle flow, and analyzing the power requirements for steady-state translocation relevant to biological and microfluidic systems.
Contribution
It introduces a combined molecular dynamics and statistical theory approach to distinguish transport regimes and quantify power needs in crowded nanochannels with no external energy input.
Findings
Two transport regimes: individual diffusion and crowded saturation.
Resistance force increases with crowding due to osmotic pressure.
Power consumption scales with channel length and transport rate.
Abstract
The problem of transport through nanochannels is one of the major questions in cell biology, with a wide range of applications. Brownian ratchets are fundamental in various biochemical processes, and are roughly divided into two categories: active (usually ATP-powered) molecular motors and passive constructions with a directional bias, where the transport is driven by thermal motion. In this paper we discuss the latter process, of spontaneous translocation of molecules (Brownian particles) by ratcheted diffusion with no external energy input: a problem relevant for protein translocation along bacterial flagella or injectosome complex, or DNA translocation by bacteriophages. We use molecular dynamics simulations and statistical theory to identify two regimes of transport: at low rate of particles injection into the channel the process is controlled by the individual diffusion towards the…
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