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Physicochemical Nature of SARS-CoV-2 Spike Protein Binding to Human Vimentin
[Image: see text] Vimentin, a protein that builds part of the cytoskeleton and is involved in many aspects of cellular function, was recently identified as a cell surface attachment site for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The present study investigated the physicoc...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10360031/ https://www.ncbi.nlm.nih.gov/pubmed/37413693 http://dx.doi.org/10.1021/acsami.3c03347 |
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author | Deptuła, Piotr Fiedoruk, Krzysztof Wasilewska, Monika Suprewicz, Łukasz Cieśluk, Mateusz Żeliszewska, Paulina Oćwieja, Magdalena Adamczyk, Zbigniew Pogoda, Katarzyna Bucki, Robert |
author_facet | Deptuła, Piotr Fiedoruk, Krzysztof Wasilewska, Monika Suprewicz, Łukasz Cieśluk, Mateusz Żeliszewska, Paulina Oćwieja, Magdalena Adamczyk, Zbigniew Pogoda, Katarzyna Bucki, Robert |
author_sort | Deptuła, Piotr |
collection | PubMed |
description | [Image: see text] Vimentin, a protein that builds part of the cytoskeleton and is involved in many aspects of cellular function, was recently identified as a cell surface attachment site for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The present study investigated the physicochemical nature of the binding between the SARS-CoV-2 S1 glycoprotein receptor binding domain (S1 RBD) and human vimentin using atomic force microscopy and a quartz crystal microbalance. The molecular interactions of S1 RBD and vimentin proteins were quantified using vimentin monolayers attached to the cleaved mica or a gold microbalance sensor as well as in its native extracellular form present on the live cell surface. The presence of specific interactions between vimentin and S1 RBD was also confirmed using in silico studies. This work provides new evidence that cell-surface vimentin (CSV) functions as a site for SARS-CoV-2 virus attachment and is involved in the pathogenesis of Covid-19, providing a potential target for therapeutic countermeasures. |
format | Online Article Text |
id | pubmed-10360031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-103600312023-07-22 Physicochemical Nature of SARS-CoV-2 Spike Protein Binding to Human Vimentin Deptuła, Piotr Fiedoruk, Krzysztof Wasilewska, Monika Suprewicz, Łukasz Cieśluk, Mateusz Żeliszewska, Paulina Oćwieja, Magdalena Adamczyk, Zbigniew Pogoda, Katarzyna Bucki, Robert ACS Appl Mater Interfaces [Image: see text] Vimentin, a protein that builds part of the cytoskeleton and is involved in many aspects of cellular function, was recently identified as a cell surface attachment site for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The present study investigated the physicochemical nature of the binding between the SARS-CoV-2 S1 glycoprotein receptor binding domain (S1 RBD) and human vimentin using atomic force microscopy and a quartz crystal microbalance. The molecular interactions of S1 RBD and vimentin proteins were quantified using vimentin monolayers attached to the cleaved mica or a gold microbalance sensor as well as in its native extracellular form present on the live cell surface. The presence of specific interactions between vimentin and S1 RBD was also confirmed using in silico studies. This work provides new evidence that cell-surface vimentin (CSV) functions as a site for SARS-CoV-2 virus attachment and is involved in the pathogenesis of Covid-19, providing a potential target for therapeutic countermeasures. American Chemical Society 2023-07-06 /pmc/articles/PMC10360031/ /pubmed/37413693 http://dx.doi.org/10.1021/acsami.3c03347 Text en © 2023 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 | Deptuła, Piotr Fiedoruk, Krzysztof Wasilewska, Monika Suprewicz, Łukasz Cieśluk, Mateusz Żeliszewska, Paulina Oćwieja, Magdalena Adamczyk, Zbigniew Pogoda, Katarzyna Bucki, Robert Physicochemical Nature of SARS-CoV-2 Spike Protein Binding to Human Vimentin |
title | Physicochemical Nature
of SARS-CoV-2 Spike
Protein Binding to Human Vimentin |
title_full | Physicochemical Nature
of SARS-CoV-2 Spike
Protein Binding to Human Vimentin |
title_fullStr | Physicochemical Nature
of SARS-CoV-2 Spike
Protein Binding to Human Vimentin |
title_full_unstemmed | Physicochemical Nature
of SARS-CoV-2 Spike
Protein Binding to Human Vimentin |
title_short | Physicochemical Nature
of SARS-CoV-2 Spike
Protein Binding to Human Vimentin |
title_sort | physicochemical nature
of sars-cov-2 spike
protein binding to human vimentin |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10360031/ https://www.ncbi.nlm.nih.gov/pubmed/37413693 http://dx.doi.org/10.1021/acsami.3c03347 |
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