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Ethanol Inactivation of Enveloped Viruses: Structural and Surface Chemistry Insights into Phi6
Department of Chemistry, University of Fribourg, Fribourg, Switzerland; Laboratory for Biointerfaces, Empa, Swiss Federal Laboratories for Material Science and Technology, St. Gallen, Switzerland.
Umeå University, Faculty of Science and Technology, Department of Chemistry.ORCID iD: 0000-0003-2646-8501
Department of Chemistry, University of Fribourg, Fribourg, Switzerland.
2021 (English)In: The Journal of Physical Chemistry Letters, E-ISSN 1948-7185, Vol. 12, no 39, p. 9557-9563Article in journal (Refereed) Published
Abstract [en]

Lipid-enveloped viruses, such as Ebola, influenza, or coronaviruses, are a major threat to human health. Ethanol is an efficient disinfectant that is widely used to inactivate these viruses and prevent their transmission. However, the interactions between ethanol and enveloped viruses leading to their inactivation are not yet fully understood. This study demonstrates the link between ethanol-induced viral inactivation and the nanostructural and chemical transformations of the model virus Phi6, an 85 nm diameter lipid-enveloped bacterial virus that is commonly used as surrogate for human pathogenic viruses. The virus morphology was investigated using small-angle X-ray scattering and dynamic light scattering and was related to its infectivity. The Phi6’s surface chemistry was characterized by cryogenic X-ray photoelectron spectroscopy, and the modifications in protein structure were assessed by circular dichroism and fluorescence spectroscopy. Ethanol-triggered structural modifications were found in the lipid envelope, detaching from the protein capsid and forming coexisting nanostructures.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2021. Vol. 12, no 39, p. 9557-9563
Keywords [en]
Vesicles, Lipids, Viruses, Ethanol, Protein structure
National Category
Microbiology Microbiology in the medical area Infectious Medicine
Identifiers
URN: urn:nbn:se:umu:diva-188601DOI: 10.1021/acs.jpclett.1c02327ISI: 000707046300021PubMedID: 34581569Scopus ID: 2-s2.0-85117219974OAI: oai:DiVA.org:umu-188601DiVA, id: diva2:1603042
Available from: 2021-10-14 Created: 2021-10-14 Last updated: 2024-07-04Bibliographically approved

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Ramstedt, Madeleine

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