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Updated: Jul 19, 2025

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Engineering Antiviral Agents via Surface Plasmon Resonance
Published on: June 14, 2022
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在人类受体识别中,SARS-CoV-2 omicron 的结构演变
Wei Zhang1,2, Ke Shi3, Qibin Geng1,2
1Department of Pharmacology, University of Minnesota Medical School , Minneapolis, Minnesota, USA.
Journal of virology
|August 14, 2023
概括
SARS-CoV-2的欧米克朗进化是由非人类动物和免疫规避驱动的. 对适应人类和小鼠ACE2的欧米克龙亚变体中受体结合域 (RBD) 的结构分析揭示了关键的进化见解.
科学领域:
- 病毒学 病毒学
- 结构生物学 结构生物学
- 进化生物学 进化生物学
背景情况:
- 持续演变的SARS-CoV-2欧米克朗亚型对大流行控制提出了挑战.
- 了解驱动欧米克朗适应的分子机制对于预测未来的病毒轨迹至关重要.
研究的目的:
- 阐明SARS-CoV-2欧米克朗亚型的受体结合域 (RBD) 的结构适应.
- 调查非人类动物和免疫逃避在奥米克朗的进化历史中的作用.
主要方法:
- 来自与人类ACE2复合的欧米克朗亚变体 (XBB.1,XBB.1.5,XBB.1.9.1) 的RBDs的确定晶体结构2.
- 分析了RBD残留物的结构变化及其适应人类和小鼠ACE2.
主要成果:
- 特定的RBD残留物 (例如493,496) 显示了人类ACE2适应的转变,与小鼠ACE2适应在早期的Omicron相关,这表明非人类动物的作用.
- 剩余486的适应变化很大,后来的变化可能与免疫逃避有关,这表明不同阶段存在不同的进化压力.
结论:
- 非人类动物宿主可能促进了早期欧米克朗亚型的进化.
- 免疫逃避似乎是后来的奥米克朗亚型的进化的一个重要驱动因素.
- 非人类动物的联合压力和免疫逃避塑造了SARS-CoV-2的进化轨迹.
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