Detailed Information on Publication Record
2021
Cargo Release from Nonenveloped Viruses and Virus-like Nanoparticles: Capsid Rupture or Pore Formation
SUKENÍK, Lukáš, Liya MUKHAMEDOVA, Michaela PROCHÁZKOVÁ, Karel ŠKUBNÍK, Pavel PLEVKA et. al.Basic information
Original name
Cargo Release from Nonenveloped Viruses and Virus-like Nanoparticles: Capsid Rupture or Pore Formation
Authors
SUKENÍK, Lukáš (203 Czech Republic, belonging to the institution), Liya MUKHAMEDOVA (643 Russian Federation, belonging to the institution), Michaela PROCHÁZKOVÁ (203 Czech Republic, belonging to the institution), Karel ŠKUBNÍK (203 Czech Republic, belonging to the institution), Pavel PLEVKA (203 Czech Republic, belonging to the institution) and Robert VÁCHA (203 Czech Republic, guarantor, belonging to the institution)
Edition
ACS Nano, Washington, D.C. American Chemical Society, 2021, 1936-0851
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10607 Virology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 18.027
RIV identification code
RIV/00216224:14740/21:00119475
Organization unit
Central European Institute of Technology
UT WoS
000731055900001
Keywords in English
virus-like nanoparticlesRNA virusgenome releasecapsidcomputer simulationscoarse-grained modelcryo-EM
Tags
International impact, Reviewed
Změněno: 27/10/2024 14:16, Ing. Martina Blahová
Abstract
V originále
Virus-like nanoparticles are protein shells similar to wild-type viruses, and both aim to deliver their content into a cell. Unfortunately, the release mechanism of their cargo/genome remains elusive. Pores on the symmetry axes were proposed to enable the slow release of the viral genome. In contrast, cryo-EM images showed that capsids of nonenveloped RNA viruses can crack open and rapidly release the genome. We combined in vitro cryo-EM observations of the genome release of three viruses with coarse-grained simulations of generic virus-like nanoparticles to investigate the cargo/genome release pathways. Simulations provided details on both slow and rapid release pathways, including the success rates of individual releases. Moreover, the simulated structures from the rapid release pathway were in agreement with the experiment. Slow release occurred when interactions between capsid subunits were long-ranged, and the cargo/genome was noncompact. In contrast, rapid release was preferred when the interaction range was short and/or the cargo/genome was compact. These findings indicate a design strategy of virus-like nanoparticles for drug delivery.
Links
GA20-20152S, research and development project |
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GX19-25982X, research and development project |
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LL2007, research and development project |
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LM2015085, research and development project |
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90070, large research infrastructures |
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90127, large research infrastructures |
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