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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...

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Autores principales: SENAPATI, SABYASACHI, BANERJEE, PRATIBHA, BHAGAVATULA, SANDILYA, KUSHWAHA, PREM PRAKASH, KUMAR, SHASHANK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2021
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.
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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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