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Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation
Living systems can experience time‐dependent dynamic self‐assembly for periodic, adaptive behavior via energy dissipation pathway. Creating in vitro mimics is a daunting mission. Here a “living” giant vesicle system that can perform a periodic pulsating motion using adenosine‐5'‐triphosphate (A...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867064/ https://www.ncbi.nlm.nih.gov/pubmed/29593961 http://dx.doi.org/10.1002/advs.201700591 |
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author | Hao, Xiang Chen, Liang Sang, Wei Yan, Qiang |
author_facet | Hao, Xiang Chen, Liang Sang, Wei Yan, Qiang |
author_sort | Hao, Xiang |
collection | PubMed |
description | Living systems can experience time‐dependent dynamic self‐assembly for periodic, adaptive behavior via energy dissipation pathway. Creating in vitro mimics is a daunting mission. Here a “living” giant vesicle system that can perform a periodic pulsating motion using adenosine‐5'‐triphosphate (ATP)‐fuelled dissipative self‐assembly is described. This dynamic system is built on transient supramolecular interactions between the polymer and cellular energy currency ATP. The vesicles capturing ATPs will deviate away from equilibrium, leading to an energy ascent that drives a continuous vesicular expansion, until a competitive ATP hydrolysis predominates to break the ATP–polymer interactions and deplete the energy stored in the vesicles, leading to an opposing vesicular contraction. The input of ATP energy can sustain that these vesicles run periodically along this reciprocating expansile–contractile process, resembling a “pulsating” behavior. ATP level can orchestrate the rhythm, amplitude, and lifetime of this biomimetic pulsation. By pre‐programming the ATP stimulation protocol, this kind of adaptive microcapsules can function as high‐performance microseparators to perform size‐selective sieving of different nanoparticles through ATP‐mediated transmembrane traffic. This man‐made system offers a primitive model of time‐dependent dynamic self‐assembly and may offer new ways to build life‐like materials with biomimetic functions. |
format | Online Article Text |
id | pubmed-5867064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58670642018-03-28 Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation Hao, Xiang Chen, Liang Sang, Wei Yan, Qiang Adv Sci (Weinh) Full Papers Living systems can experience time‐dependent dynamic self‐assembly for periodic, adaptive behavior via energy dissipation pathway. Creating in vitro mimics is a daunting mission. Here a “living” giant vesicle system that can perform a periodic pulsating motion using adenosine‐5'‐triphosphate (ATP)‐fuelled dissipative self‐assembly is described. This dynamic system is built on transient supramolecular interactions between the polymer and cellular energy currency ATP. The vesicles capturing ATPs will deviate away from equilibrium, leading to an energy ascent that drives a continuous vesicular expansion, until a competitive ATP hydrolysis predominates to break the ATP–polymer interactions and deplete the energy stored in the vesicles, leading to an opposing vesicular contraction. The input of ATP energy can sustain that these vesicles run periodically along this reciprocating expansile–contractile process, resembling a “pulsating” behavior. ATP level can orchestrate the rhythm, amplitude, and lifetime of this biomimetic pulsation. By pre‐programming the ATP stimulation protocol, this kind of adaptive microcapsules can function as high‐performance microseparators to perform size‐selective sieving of different nanoparticles through ATP‐mediated transmembrane traffic. This man‐made system offers a primitive model of time‐dependent dynamic self‐assembly and may offer new ways to build life‐like materials with biomimetic functions. John Wiley and Sons Inc. 2018-01-04 /pmc/articles/PMC5867064/ /pubmed/29593961 http://dx.doi.org/10.1002/advs.201700591 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Hao, Xiang Chen, Liang Sang, Wei Yan, Qiang Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation |
title | Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation |
title_full | Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation |
title_fullStr | Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation |
title_full_unstemmed | Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation |
title_short | Periodically Self‐Pulsating Microcapsule as Programmed Microseparator via ATP‐Regulated Energy Dissipation |
title_sort | periodically self‐pulsating microcapsule as programmed microseparator via atp‐regulated energy dissipation |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867064/ https://www.ncbi.nlm.nih.gov/pubmed/29593961 http://dx.doi.org/10.1002/advs.201700591 |
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