Ratcheted diffusion transport through crowded nanochannels

The problem of transport through nanochannels is one of the major questions in cell biology, with a wide range of applications. In this paper we discuss the process of spontaneous translocation of molecules (Brownian particles) by ratcheted diffusion: a problem relevant for protein translocation alo...

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Main Authors: Lappala, Anna, Zaccone, Alessio, Terentjev, Eugene M.
Format: Online
Language:English
Published: Nature Publishing Group 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813928/
id pubmed-3813928
recordtype oai_dc
spelling pubmed-38139282013-10-31 Ratcheted diffusion transport through crowded nanochannels Lappala, Anna Zaccone, Alessio Terentjev, Eugene M. Article The problem of transport through nanochannels is one of the major questions in cell biology, with a wide range of applications. In this paper we discuss the process of spontaneous translocation of molecules (Brownian particles) by ratcheted diffusion: 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 particle injection into the channel the process is controlled by the individual diffusion towards the open end (the first passage problem), while at a higher rate of injection the crowded regime sets in. In this regime the particle density in the channel reaches a constant saturation level and the resistance force increases substantially, due to the osmotic pressure build-up. To achieve a steady-state transport, the apparatus that injects new particles into a crowded channel has to operate with an increasing power consumption, proportional to the length of the channel and the required rate of transport. The analysis of resistance force, and accordingly – the power required to inject the particles into a crowded channel to overcome its clogging, is also relevant for many microfluidics applications. Nature Publishing Group 2013-10-31 /pmc/articles/PMC3813928/ /pubmed/24173137 http://dx.doi.org/10.1038/srep03103 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Lappala, Anna
Zaccone, Alessio
Terentjev, Eugene M.
spellingShingle Lappala, Anna
Zaccone, Alessio
Terentjev, Eugene M.
Ratcheted diffusion transport through crowded nanochannels
author_facet Lappala, Anna
Zaccone, Alessio
Terentjev, Eugene M.
author_sort Lappala, Anna
title Ratcheted diffusion transport through crowded nanochannels
title_short Ratcheted diffusion transport through crowded nanochannels
title_full Ratcheted diffusion transport through crowded nanochannels
title_fullStr Ratcheted diffusion transport through crowded nanochannels
title_full_unstemmed Ratcheted diffusion transport through crowded nanochannels
title_sort ratcheted diffusion transport through crowded nanochannels
description The problem of transport through nanochannels is one of the major questions in cell biology, with a wide range of applications. In this paper we discuss the process of spontaneous translocation of molecules (Brownian particles) by ratcheted diffusion: 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 particle injection into the channel the process is controlled by the individual diffusion towards the open end (the first passage problem), while at a higher rate of injection the crowded regime sets in. In this regime the particle density in the channel reaches a constant saturation level and the resistance force increases substantially, due to the osmotic pressure build-up. To achieve a steady-state transport, the apparatus that injects new particles into a crowded channel has to operate with an increasing power consumption, proportional to the length of the channel and the required rate of transport. The analysis of resistance force, and accordingly – the power required to inject the particles into a crowded channel to overcome its clogging, is also relevant for many microfluidics applications.
publisher Nature Publishing Group
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813928/
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