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ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity
The susceptibility of different populations to SARS-CoV-2 infection is not yet understood. Here, we combined ACE2 coding variants' analysis in different populations and computational chemistry calculations to probe the effects on SARS-CoV-2/ACE2 interaction. ACE2-K26R; which is most frequent in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439997/ https://www.ncbi.nlm.nih.gov/pubmed/32844124 http://dx.doi.org/10.1016/j.bbrep.2020.100798 |
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author | Ali, Fedaa Elserafy, Menattallah Alkordi, Mohamed H. Amin, Muhamed |
author_facet | Ali, Fedaa Elserafy, Menattallah Alkordi, Mohamed H. Amin, Muhamed |
author_sort | Ali, Fedaa |
collection | PubMed |
description | The susceptibility of different populations to SARS-CoV-2 infection is not yet understood. Here, we combined ACE2 coding variants' analysis in different populations and computational chemistry calculations to probe the effects on SARS-CoV-2/ACE2 interaction. ACE2-K26R; which is most frequent in Ashkenazi Jewish population decreased the SARS-CoV-2/ACE2 electrostatic attraction. On the contrary, ACE2-I468V, R219C, K341R, D206G, G211R increased the electrostatic attraction; ordered by binding strength from weakest to strongest. The aforementioned variants are most frequent in East Asian, South Asian, African and African American, European, European and South Asian populations, respectively. |
format | Online Article Text |
id | pubmed-7439997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74399972020-08-21 ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity Ali, Fedaa Elserafy, Menattallah Alkordi, Mohamed H. Amin, Muhamed Biochem Biophys Rep Research Article The susceptibility of different populations to SARS-CoV-2 infection is not yet understood. Here, we combined ACE2 coding variants' analysis in different populations and computational chemistry calculations to probe the effects on SARS-CoV-2/ACE2 interaction. ACE2-K26R; which is most frequent in Ashkenazi Jewish population decreased the SARS-CoV-2/ACE2 electrostatic attraction. On the contrary, ACE2-I468V, R219C, K341R, D206G, G211R increased the electrostatic attraction; ordered by binding strength from weakest to strongest. The aforementioned variants are most frequent in East Asian, South Asian, African and African American, European, European and South Asian populations, respectively. Elsevier 2020-08-20 /pmc/articles/PMC7439997/ /pubmed/32844124 http://dx.doi.org/10.1016/j.bbrep.2020.100798 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Ali, Fedaa Elserafy, Menattallah Alkordi, Mohamed H. Amin, Muhamed ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity |
title | ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity |
title_full | ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity |
title_fullStr | ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity |
title_full_unstemmed | ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity |
title_short | ACE2 coding variants in different populations and their potential impact on SARS-CoV-2 binding affinity |
title_sort | ace2 coding variants in different populations and their potential impact on sars-cov-2 binding affinity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439997/ https://www.ncbi.nlm.nih.gov/pubmed/32844124 http://dx.doi.org/10.1016/j.bbrep.2020.100798 |
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