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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...

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Autores principales: Deptuła, Piotr, Fiedoruk, Krzysztof, Wasilewska, Monika, Suprewicz, Łukasz, Cieśluk, Mateusz, Żeliszewska, Paulina, Oćwieja, Magdalena, Adamczyk, Zbigniew, Pogoda, Katarzyna, Bucki, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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