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鉴定SARS-CoV-2蛋白域和人类联体之间的基于动机的相互作用,可以确定抗病毒标
Filip Mihalič1, Caroline Benz2, Eszter Kassa2
1Department of Medical Biochemistry and Microbiology, Uppsala University, Box 582, Husargatan 3, 751 23, Uppsala, Sweden.
Nature communications
|September 13, 2023
概括
这项研究确定了与SARS-CoV-2蛋白相互作用的人类蛋白质区域,发现了抑制病毒复制的两个. 这些发现突出了潜在的抗病毒策略和病毒蛋白对细胞通路的广泛影响.
科学领域:
- 病毒学 病毒学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 主体-病毒蛋白-蛋白相互作用对于病毒复制至关重要.
- 这些相互作用通常涉及与内在无序的蛋白质区域 (IDRs) 与折叠的蛋白质域结合.
- 了解这些相互作用可以揭示治疗目标.
研究的目的:
- 为了识别与SARS-CoV-2蛋白结合的人类IDRs.
- 为了发现新的抗病毒.
- 研究病毒蛋白对宿主细胞通路的影响.
主要方法:
- 蛋白质菌体显示器 (ProP-PD) 用于选人类蛋白质组的IDR.
- 鉴定到的相互作用的结合亲缘关系用解离常数 (KD) 来量化.
- 确定了-蛋白相互作用的关键特异性残留物.
主要成果:
- 来自IDR的281个人类被发现与SARS-CoV-2蛋白质的11个折叠域结合.
- 确定了31种相互作用的亲和度测量 (KD ∼ 7300 μM).
- 两个已识别的,结合NSP9和NSP16,证明了病毒复制的抑制.
结论:
- 高通量结屏对于识别宿主病毒相互作用和抗病毒是有效的.
- 针对NSP9和NSP16的已识别的体代表了潜在的抗病毒疗法.
- 许多低亲和度的相互作用表明,SARS-CoV-2蛋白可能会大大破坏宿主细胞通路.
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