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Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is at present an emerging global public health crisis. Angiotensin converting enzyme 2 (ACE2) and trans-membrane protease serine 2 (TMPRSS2) are the two major host factors that contribute to the virulence of SARS-CoV-2 and pathog...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904510/ https://www.ncbi.nlm.nih.gov/pubmed/33707363 http://dx.doi.org/10.1007/s12041-021-01262-w |
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author | SENAPATI, SABYASACHI BANERJEE, PRATIBHA BHAGAVATULA, SANDILYA KUSHWAHA, PREM PRAKASH KUMAR, SHASHANK |
author_facet | SENAPATI, SABYASACHI BANERJEE, PRATIBHA BHAGAVATULA, SANDILYA KUSHWAHA, PREM PRAKASH KUMAR, SHASHANK |
author_sort | SENAPATI, SABYASACHI |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is at present an emerging global public health crisis. Angiotensin converting enzyme 2 (ACE2) and trans-membrane protease serine 2 (TMPRSS2) are the two major host factors that contribute to the virulence of SARS-CoV-2 and pathogenesis of coronavirus disease-19 (COVID-19). Transmission of SARS-CoV-2 from animal to human is considered a rare event that necessarily requires strong evolutionary adaptations. Till date no other human cellular receptors are identified beside ACE2 for SARS-CoV-2 entry inside the human cell. Proteolytic cleavage of viral spike (S)-protein and ACE2 by TMPRSS2 began the entire host–pathogen interaction initiated with the physical binding of ACE2 to S-protein. SARS-CoV-2 S-protein binds to ACE2 with much higher affinity and stability than that of SARS-CoVs. Molecular interactions between ACE2-S and TMPRSS2-S are crucial and preciously mediated by specific residues. Structural stability, binding affinity and level of expression of these three interacting proteins are key susceptibility factors for COVID-19. Specific protein–protein interactions (PPI) are being identified that explains uniqueness of SARS-CoV-2 infection. Amino acid substitutions due to naturally occurring genetic polymorphisms potentially alter these PPIs and poses further clinical heterogeneity of COVID-19. Repurposing of several phytochemicals and approved drugs against ACE2, TMPRSS2 and S-protein have been proposed that could inhibit PPI between them. We have also identified some novel lead phytochemicals present in Azadirachta indica and Aloe barbadensis which could be utilized for further in vitro and in vivo anti-COVID-19 drug discovery. Uncovering details of ACE2-S and TMPRSS2-S interactions would further contribute to future research on COVID-19. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12041-021-01262-w) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7904510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-79045102021-02-25 Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 SENAPATI, SABYASACHI BANERJEE, PRATIBHA BHAGAVATULA, SANDILYA KUSHWAHA, PREM PRAKASH KUMAR, SHASHANK J Genet Review Article Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is at present an emerging global public health crisis. Angiotensin converting enzyme 2 (ACE2) and trans-membrane protease serine 2 (TMPRSS2) are the two major host factors that contribute to the virulence of SARS-CoV-2 and pathogenesis of coronavirus disease-19 (COVID-19). Transmission of SARS-CoV-2 from animal to human is considered a rare event that necessarily requires strong evolutionary adaptations. Till date no other human cellular receptors are identified beside ACE2 for SARS-CoV-2 entry inside the human cell. Proteolytic cleavage of viral spike (S)-protein and ACE2 by TMPRSS2 began the entire host–pathogen interaction initiated with the physical binding of ACE2 to S-protein. SARS-CoV-2 S-protein binds to ACE2 with much higher affinity and stability than that of SARS-CoVs. Molecular interactions between ACE2-S and TMPRSS2-S are crucial and preciously mediated by specific residues. Structural stability, binding affinity and level of expression of these three interacting proteins are key susceptibility factors for COVID-19. Specific protein–protein interactions (PPI) are being identified that explains uniqueness of SARS-CoV-2 infection. Amino acid substitutions due to naturally occurring genetic polymorphisms potentially alter these PPIs and poses further clinical heterogeneity of COVID-19. Repurposing of several phytochemicals and approved drugs against ACE2, TMPRSS2 and S-protein have been proposed that could inhibit PPI between them. We have also identified some novel lead phytochemicals present in Azadirachta indica and Aloe barbadensis which could be utilized for further in vitro and in vivo anti-COVID-19 drug discovery. Uncovering details of ACE2-S and TMPRSS2-S interactions would further contribute to future research on COVID-19. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12041-021-01262-w) contains supplementary material, which is available to authorized users. Springer India 2021-02-25 2021 /pmc/articles/PMC7904510/ /pubmed/33707363 http://dx.doi.org/10.1007/s12041-021-01262-w Text en © Indian Academy of Sciences 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article SENAPATI, SABYASACHI BANERJEE, PRATIBHA BHAGAVATULA, SANDILYA KUSHWAHA, PREM PRAKASH KUMAR, SHASHANK Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 |
title | Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 |
title_full | Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 |
title_fullStr | Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 |
title_full_unstemmed | Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 |
title_short | Contributions of human ACE2 and TMPRSS2 in determining host–pathogen interaction of COVID-19 |
title_sort | contributions of human ace2 and tmprss2 in determining host–pathogen interaction of covid-19 |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904510/ https://www.ncbi.nlm.nih.gov/pubmed/33707363 http://dx.doi.org/10.1007/s12041-021-01262-w |
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