利用工程脂质体提取新型冠状病毒的尖峰来中和新型冠状病毒

IF 4.7 4区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zhenjiang Zhang Ph.D., Michael R. King Ph.D.
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引用次数: 0

摘要

毁灭性的COVID-19大流行促使开发安全有效的抗病毒药物,以降低与感染相关的发病率和死亡率。我们开发了纳米级脂质体,它们被严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的细胞受体包裹,SARS-CoV-2是导致COVID-19的病毒。构建了带有SARS-CoV-2刺突蛋白假型的慢病毒颗粒,并用于测试工程脂质体的病毒中和潜力。在透射电镜下,我们首次观察到假病毒纯化时刺突蛋白从假病毒表面解离。脂质体通过从假病毒表面提取刺突蛋白有效地抑制病毒进入宿主细胞。由于脂质体表面的受体可以很容易地改变以靶向其他病毒,因此受体包被脂质体代表了一种很有前途的广谱抗病毒开发策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neutralization of the new coronavirus by extracting their spikes using engineered liposomes

Neutralization of the new coronavirus by extracting their spikes using engineered liposomes

The devastating COVID-19 pandemic motivates the development of safe and effective antivirals to reduce morbidity and mortality associated with infection. We developed nanoscale liposomes that are coated with the cell receptor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes COVID-19. Lentiviral particles pseudotyped with the spike protein of SARS-CoV-2 were constructed and used to test the virus neutralization potential of the engineered liposomes. Under TEM, we observed for the first time a dissociation of spike proteins from the pseudovirus surface when the pseudovirus was purified. The liposomes potently inhibit viral entry into host cells by extracting the spike proteins from the pseudovirus surface. As the receptor on the liposome surface can be readily changed to target other viruses, the receptor-coated liposome represents a promising strategy for broad spectrum antiviral development.

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来源期刊
CiteScore
8.10
自引率
3.60%
发文量
104
审稿时长
4.6 months
期刊介绍: Nanomedicine: Nanotechnology, Biology and Medicine (NBM) is an international, peer-reviewed journal presenting novel, significant, and interdisciplinary theoretical and experimental results related to nanoscience and nanotechnology in the life and health sciences. Content includes basic, translational, and clinical research addressing diagnosis, treatment, monitoring, prediction, and prevention of diseases.
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