Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern

One year since the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was reported in China, several variants of concern (VOC) have appeared around the world, with some variants seeming to pose a greater thread to public health due to enhanced transmissibility or infectivity. This st...

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Main Authors: Nariman Shahhosseini, George (Giorgi) Babuadze, Gary Wong, Gary P. Kobinger
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/9/5/926
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spelling doaj-772931b646024e7c909295509e263dc22021-04-26T23:01:25ZengMDPI AGMicroorganisms2076-26072021-04-01992692610.3390/microorganisms9050926Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of ConcernNariman Shahhosseini0George (Giorgi) Babuadze1Gary Wong2Gary P. Kobinger3Département de Microbiologie-Infectiologie et d’Immunologie, Université Laval, Québec City, QC G1V4G2, CanadaDepartment of Biological Sciences, Sunnybrook Research Institute, University of Toronto, Toronto, ON M4N3M5, CanadaDépartement de Microbiologie-Infectiologie et d’Immunologie, Université Laval, Québec City, QC G1V4G2, CanadaDépartement de Microbiologie-Infectiologie et d’Immunologie, Université Laval, Québec City, QC G1V4G2, CanadaOne year since the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was reported in China, several variants of concern (VOC) have appeared around the world, with some variants seeming to pose a greater thread to public health due to enhanced transmissibility or infectivity. This study provides a framework for molecular characterization of novel VOC and investigates the effect of mutations on the binding affinity of the receptor-binding domain (RBD) to human angiotensin-converting enzyme 2 (hACE2) using in silico approach. Notable nonsynonymous mutations in RBD of VOC include the E484K and K417N/T that can be seen in South African and Brazilian variants, and N501Y and D614G that can be seen in all VOC. Phylogenetic analyses demonstrated that although the UK-VOC and the BR-VOC fell in the clade GR, they have different mutation signatures, implying an independent evolutionary pathway. The same is true about SA-VOC and COH-VOC felling in clade GH, but different mutation signatures. Combining molecular interaction modeling and the free energy of binding (FEB) calculations for VOC, it can be assumed that the mutation N501Y has the highest binding affinity in RBD for all VOC, followed by E484K (only for BR-VOC), which favors the formation of a stable complex. However, mutations at the residue K417N/T are shown to reduce the binding affinity. Once vaccination has started, there will be selective pressure that would be in favor of emergence of novel variants capable of escaping the immune system. Therefore, genomic surveillance should be enhanced to find and monitor new emerging SARS-CoV-2 variants before they become a public health concern.https://www.mdpi.com/2076-2607/9/5/926SARS-CoV-2variants of concernmutationmolecular interactionbinding free energy
collection DOAJ
language English
format Article
sources DOAJ
author Nariman Shahhosseini
George (Giorgi) Babuadze
Gary Wong
Gary P. Kobinger
spellingShingle Nariman Shahhosseini
George (Giorgi) Babuadze
Gary Wong
Gary P. Kobinger
Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern
Microorganisms
SARS-CoV-2
variants of concern
mutation
molecular interaction
binding free energy
author_facet Nariman Shahhosseini
George (Giorgi) Babuadze
Gary Wong
Gary P. Kobinger
author_sort Nariman Shahhosseini
title Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern
title_short Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern
title_full Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern
title_fullStr Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern
title_full_unstemmed Mutation Signatures and In Silico Docking of Novel SARS-CoV-2 Variants of Concern
title_sort mutation signatures and in silico docking of novel sars-cov-2 variants of concern
publisher MDPI AG
series Microorganisms
issn 2076-2607
publishDate 2021-04-01
description One year since the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was reported in China, several variants of concern (VOC) have appeared around the world, with some variants seeming to pose a greater thread to public health due to enhanced transmissibility or infectivity. This study provides a framework for molecular characterization of novel VOC and investigates the effect of mutations on the binding affinity of the receptor-binding domain (RBD) to human angiotensin-converting enzyme 2 (hACE2) using in silico approach. Notable nonsynonymous mutations in RBD of VOC include the E484K and K417N/T that can be seen in South African and Brazilian variants, and N501Y and D614G that can be seen in all VOC. Phylogenetic analyses demonstrated that although the UK-VOC and the BR-VOC fell in the clade GR, they have different mutation signatures, implying an independent evolutionary pathway. The same is true about SA-VOC and COH-VOC felling in clade GH, but different mutation signatures. Combining molecular interaction modeling and the free energy of binding (FEB) calculations for VOC, it can be assumed that the mutation N501Y has the highest binding affinity in RBD for all VOC, followed by E484K (only for BR-VOC), which favors the formation of a stable complex. However, mutations at the residue K417N/T are shown to reduce the binding affinity. Once vaccination has started, there will be selective pressure that would be in favor of emergence of novel variants capable of escaping the immune system. Therefore, genomic surveillance should be enhanced to find and monitor new emerging SARS-CoV-2 variants before they become a public health concern.
topic SARS-CoV-2
variants of concern
mutation
molecular interaction
binding free energy
url https://www.mdpi.com/2076-2607/9/5/926
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