奥密克戎变异株和严重急性呼吸综合征冠状病毒2受体结合域与血管紧张素转换酶2受体静电相互作用的变化

R. Mungmunpuntipantip, V. Wiwanitkit
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引用次数: 0

摘要

背景严重急性呼吸综合征冠状病毒2型(严重急性呼吸系统综合征冠状病毒冠状病毒2型)变异株目前是一种新的危险。自2019年末经典的严重急性呼吸系统综合征冠状病毒2型首次出现以来,病原体的基因改变不断发生,一些新的危险形式已经出现。导致临床问题的潜在病理生理过程是由基因突变引起的分子变化。目的测定奥密克戎变异株严重急性呼吸系统综合征冠状病毒2型受体结合结构域与血管紧张素转换酶2(ACE2)相互作用的变化。方法研究人员调查了SARS受体CoV2结合区的改变如何与ACE2受体静电相互作用。在这份报告中,调查了2019年三种重要的冠状病毒疾病变体,β、德尔塔和奥密克戎。结果根据这项研究,由于每种研究的变体,严重急性呼吸系统综合征冠状病毒2型的受体结合结构域与ACE2受体之间的静电相互作用都发生了变化。奥密克戎变异株的变化最大,其次是德尔塔变异株和贝塔变异株。结论我们的结果可能支持临床发现,即奥密克戎变异株比野生型和其他变异株更具传播性。
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Omicron variant and change of electrostatic interactions between receptor binding domain of severe acute respiratory syndrome coronavirus 2 with the angiotensin-converting enzyme 2 receptor
BACKGROUND Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants are currently a new hazard. Since the first appearance of classical SARS-CoV-2 in late 2019, pathogen genetic alterations have continued to occur, and some new hazardous forms have already emerged. The underlying pathophysiological process leading to clinical issue is molecular change caused by genetic mutation. AIM To determine the change in the interaction between receptor binding domain of omicron variant SARS-CoV-2 and the angiotensin-converting enzyme 2 (ACE2). METHODS The researchers investigated how alterations in the binding area of the SARS receptor CoV2 interacted electrostatically with the ACE2 receptor. In this report, three important coronavirus disease 2019 variants, beta, delta, and omicron, were investigated. RESULTS According to this study, there was a change of electrostatic interactions between the receptor binding domain of SARS-CoV-2 with the ACE2 receptor due to each studied variant. The most change was detected in omicron variant followed by delta variant and beta variant. CONCLUSION Our results may support the clinical finding that the omicron variant is more transmissible than the wild type and other variants.
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