{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["de Souza AS"],"funding":["Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico","Financiadora de Estudos e Projetos","Funda??o de Amparo ? Pesquisa do Estado de S?o Paulo","Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior"],"pagination":["30700-30709"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9437663"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["7(35)"],"pubmed_abstract":["Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is evolving with mutations in the spike protein, especially in the receptor-binding domain (RBD). The failure of public health measures in some countries to contain the spread of the disease has given rise to novel viral variants with increased transmissibility. However, key questions about how quickly the variants can spread remain unclear. Herein, we performed a structural investigation using molecular dynamics simulations and determined dissociation constant (<i>K</i> <sub>D</sub>) values using surface plasmon resonance assays of three fast-spreading SARS-CoV-2 variants, alpha, beta, and gamma, as well as genetic factors in host cells that may be related to the viral infection. Our results suggest that the SARS-CoV-2 variants "],"journal":["ACS omega"],"pubmed_title":["Molecular Dynamics Analysis of Fast-Spreading Severe Acute Respiratory Syndrome Coronavirus 2 Variants and Their Effects on the Interaction with Human Angiotensin-Converting Enzyme 2."],"pmcid":["PMC9437663"],"funding_grant_id":["2017/19541-2","2020/04680-0","2017/18246-7","2018/15579-8","88887.620198/2021-00","88887.374931/2019-00","FINEP 0459/20","2020/06091-1","2018/07366-4","2020/14158-9","2017/17636-6","2016/09047-8","2019/00195-2"],"pubmed_authors":["Dos Santos FF","de Araujo Juvenal G","Li C","Paudel P","Guzzo CR","de Souza AS","de Souza RF","Ge P","de Freitas Amorim VM","Jiang Y","Huang Y","Guardia GDA","Galante PAF","Ulrich H","Dos Santos FRC"],"additional_accession":[]},"is_claimable":false,"name":"Molecular Dynamics Analysis of Fast-Spreading Severe Acute Respiratory Syndrome Coronavirus 2 Variants and Their Effects on the Interaction with Human Angiotensin-Converting Enzyme 2.","description":"Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is evolving with mutations in the spike protein, especially in the receptor-binding domain (RBD). The failure of public health measures in some countries to contain the spread of the disease has given rise to novel viral variants with increased transmissibility. However, key questions about how quickly the variants can spread remain unclear. Herein, we performed a structural investigation using molecular dynamics simulations and determined dissociation constant (<i>K</i> <sub>D</sub>) values using surface plasmon resonance assays of three fast-spreading SARS-CoV-2 variants, alpha, beta, and gamma, as well as genetic factors in host cells that may be related to the viral infection. Our results suggest that the SARS-CoV-2 variants ","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Sep","modification":"2026-05-10T05:13:57.952Z","creation":"2025-02-19T04:03:21.74Z"},"accession":"S-EPMC9437663","cross_references":{"pubmed":["36068861"],"doi":["10.1021/acsomega.1c07240"]}}