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Quantification of the Retention and Disassembly of Virus Particles by a PEI-Functionalized Microfiltration Membrane
[Image: see text] Monitoring the performance of polymer-functionalized surfaces that aim at removing and inactivating viruses is typically labor-intensive and time-consuming. This hampers the development and optimization of such surfaces. Here we present experiments of low complexity that can be use...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275059/ https://www.ncbi.nlm.nih.gov/pubmed/35846780 http://dx.doi.org/10.1021/acsapm.2c00560 |
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author | Chatterjee, Swarupa Molenaar, Robert de Vos, Wiebe M. Roesink, Hendrik D. W. Wagterveld, R. Martijn Cornelissen, Jeroen J. L. M. Claessens, Mireille M. A. E. Blum, Christian |
author_facet | Chatterjee, Swarupa Molenaar, Robert de Vos, Wiebe M. Roesink, Hendrik D. W. Wagterveld, R. Martijn Cornelissen, Jeroen J. L. M. Claessens, Mireille M. A. E. Blum, Christian |
author_sort | Chatterjee, Swarupa |
collection | PubMed |
description | [Image: see text] Monitoring the performance of polymer-functionalized surfaces that aim at removing and inactivating viruses is typically labor-intensive and time-consuming. This hampers the development and optimization of such surfaces. Here we present experiments of low complexity that can be used to characterize and quantify the antiviral properties of polymer-functionalized surfaces. We showcase our approach on polyethylenimine (PEI)-coated poly(ether sulfone) (PES) microfiltration membranes. We use a fluorescently labeled model virus to quantify both virus removal and inactivation. We directly quantify the log removal of intact viruses by this membrane using single particle counting. Additionally, we exploit the change in photophysical properties upon disassembly of the virus to show that viruses are inactivated by the PEI coating. Although only a small fraction of intact viruses can pass the membrane, a considerable fraction of inactivated, disassembled viruses are found in the filtrate. Fluorescence microscopy experiments show that most of the viruses left behind on the microfiltration membrane are in the inactivated, disassembled state. Combined, our fluorescence microscopy and spectroscopy experiments show that not only does the model virus adsorb to the PEI coating on the membrane but also the interaction with PEI results in the disassembly of the virus capsid. |
format | Online Article Text |
id | pubmed-9275059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92750592022-07-13 Quantification of the Retention and Disassembly of Virus Particles by a PEI-Functionalized Microfiltration Membrane Chatterjee, Swarupa Molenaar, Robert de Vos, Wiebe M. Roesink, Hendrik D. W. Wagterveld, R. Martijn Cornelissen, Jeroen J. L. M. Claessens, Mireille M. A. E. Blum, Christian ACS Appl Polym Mater [Image: see text] Monitoring the performance of polymer-functionalized surfaces that aim at removing and inactivating viruses is typically labor-intensive and time-consuming. This hampers the development and optimization of such surfaces. Here we present experiments of low complexity that can be used to characterize and quantify the antiviral properties of polymer-functionalized surfaces. We showcase our approach on polyethylenimine (PEI)-coated poly(ether sulfone) (PES) microfiltration membranes. We use a fluorescently labeled model virus to quantify both virus removal and inactivation. We directly quantify the log removal of intact viruses by this membrane using single particle counting. Additionally, we exploit the change in photophysical properties upon disassembly of the virus to show that viruses are inactivated by the PEI coating. Although only a small fraction of intact viruses can pass the membrane, a considerable fraction of inactivated, disassembled viruses are found in the filtrate. Fluorescence microscopy experiments show that most of the viruses left behind on the microfiltration membrane are in the inactivated, disassembled state. Combined, our fluorescence microscopy and spectroscopy experiments show that not only does the model virus adsorb to the PEI coating on the membrane but also the interaction with PEI results in the disassembly of the virus capsid. American Chemical Society 2022-06-27 2022-07-08 /pmc/articles/PMC9275059/ /pubmed/35846780 http://dx.doi.org/10.1021/acsapm.2c00560 Text en © 2022 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 | Chatterjee, Swarupa Molenaar, Robert de Vos, Wiebe M. Roesink, Hendrik D. W. Wagterveld, R. Martijn Cornelissen, Jeroen J. L. M. Claessens, Mireille M. A. E. Blum, Christian Quantification of the Retention and Disassembly of Virus Particles by a PEI-Functionalized Microfiltration Membrane |
title | Quantification of the Retention and Disassembly of
Virus Particles by a PEI-Functionalized Microfiltration Membrane |
title_full | Quantification of the Retention and Disassembly of
Virus Particles by a PEI-Functionalized Microfiltration Membrane |
title_fullStr | Quantification of the Retention and Disassembly of
Virus Particles by a PEI-Functionalized Microfiltration Membrane |
title_full_unstemmed | Quantification of the Retention and Disassembly of
Virus Particles by a PEI-Functionalized Microfiltration Membrane |
title_short | Quantification of the Retention and Disassembly of
Virus Particles by a PEI-Functionalized Microfiltration Membrane |
title_sort | quantification of the retention and disassembly of
virus particles by a pei-functionalized microfiltration membrane |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275059/ https://www.ncbi.nlm.nih.gov/pubmed/35846780 http://dx.doi.org/10.1021/acsapm.2c00560 |
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