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Percolation Theory Reveals Biophysical Properties of Virus-like Particles

[Image: see text] The viral protein containers that encapsulate a virus’ genetic material are repurposed as virus-like particles in a host of nanotechnology applications, including cargo delivery, storage, catalysis, and vaccination. These viral architectures have evolved to sit on the knife’s edge...

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Detalles Bibliográficos
Autores principales: Brunk, Nicholas E., Twarock, Reidun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397427/
https://www.ncbi.nlm.nih.gov/pubmed/34296852
http://dx.doi.org/10.1021/acsnano.1c01882
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author Brunk, Nicholas E.
Twarock, Reidun
author_facet Brunk, Nicholas E.
Twarock, Reidun
author_sort Brunk, Nicholas E.
collection PubMed
description [Image: see text] The viral protein containers that encapsulate a virus’ genetic material are repurposed as virus-like particles in a host of nanotechnology applications, including cargo delivery, storage, catalysis, and vaccination. These viral architectures have evolved to sit on the knife’s edge between stability, to provide adequate protection for their genetic cargoes, and instability, to enable their efficient and timely release in the host cell environment upon environmental cues. By introducing a percolation theory for viral capsids, we demonstrate that the geometric characteristics of a viral capsid in terms of its subunit layout and intersubunit interaction network are key for its disassembly behavior. A comparative analysis of all alternative homogeneously tiled capsid structures of the same stoichiometry identifies evolutionary drivers favoring specific viral geometries in nature and offers a guide for virus-like particle design in nanotechnology.
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spelling pubmed-83974272021-08-31 Percolation Theory Reveals Biophysical Properties of Virus-like Particles Brunk, Nicholas E. Twarock, Reidun ACS Nano [Image: see text] The viral protein containers that encapsulate a virus’ genetic material are repurposed as virus-like particles in a host of nanotechnology applications, including cargo delivery, storage, catalysis, and vaccination. These viral architectures have evolved to sit on the knife’s edge between stability, to provide adequate protection for their genetic cargoes, and instability, to enable their efficient and timely release in the host cell environment upon environmental cues. By introducing a percolation theory for viral capsids, we demonstrate that the geometric characteristics of a viral capsid in terms of its subunit layout and intersubunit interaction network are key for its disassembly behavior. A comparative analysis of all alternative homogeneously tiled capsid structures of the same stoichiometry identifies evolutionary drivers favoring specific viral geometries in nature and offers a guide for virus-like particle design in nanotechnology. American Chemical Society 2021-07-23 2021-08-24 /pmc/articles/PMC8397427/ /pubmed/34296852 http://dx.doi.org/10.1021/acsnano.1c01882 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brunk, Nicholas E.
Twarock, Reidun
Percolation Theory Reveals Biophysical Properties of Virus-like Particles
title Percolation Theory Reveals Biophysical Properties of Virus-like Particles
title_full Percolation Theory Reveals Biophysical Properties of Virus-like Particles
title_fullStr Percolation Theory Reveals Biophysical Properties of Virus-like Particles
title_full_unstemmed Percolation Theory Reveals Biophysical Properties of Virus-like Particles
title_short Percolation Theory Reveals Biophysical Properties of Virus-like Particles
title_sort percolation theory reveals biophysical properties of virus-like particles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397427/
https://www.ncbi.nlm.nih.gov/pubmed/34296852
http://dx.doi.org/10.1021/acsnano.1c01882
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