中和Aptamers能阻断S/RBD-ACE2相互作用并防止宿主细胞感染

Xiaohui Liu, Yi-Ling Wang, Jacky Wu, Jianjun Qi, Zihua Zeng, Quanyuan Wan, Zhenghu Chen, Pragya Manandhar, Victoria S Cavener, Nina R Boyle, Xinping Fu, Eric Salazar, Suresh V Kuchipudi, Vivek Kapur, Xiaoliu Zhang, Michihisa Umetani, Mehmet Sen, Richard C Willson, Shu-Hsia Chen, Youli Zu
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引用次数: 0

摘要

严重急性呼吸系统综合征冠状病毒2尖峰(S)蛋白的受体结合域(RBD)在介导病毒感染致病的第一步中发挥着核心作用:病毒与人类宿主细胞上的血管紧张素转换酶2(ACE2)受体结合。因此,S/RBD 是预防和治疗 2019 年冠状病毒病(COVID-19)的阻断和中和疗法的理想靶点。利用基于靶点的选择方法,我们开发出了含有特异性靶向 S/RBD 的保守序列基团的寡核苷酸适配体。合成的适配体与S/RBD包被病毒模拟物具有很高的结合亲和力(K D≈7 nM),还能阻断S/RBD与ACE2受体的相互作用(IC50≈5 nM)。重要的是,aptamers能够中和表达S蛋白的病毒颗粒并阻止宿主细胞感染,这表明COVID-19治疗策略大有可为。
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Neutralizing Aptamers Block S/RBD-ACE2 Interactions and Prevent Host Cell Infection.

The receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 spike (S) protein plays a central role in mediating the first step of virus infection to cause disease: virus binding to angiotensin-converting enzyme 2 (ACE2) receptors on human host cells. Therefore, S/RBD is an ideal target for blocking and neutralization therapies to prevent and treat coronavirus disease 2019 (COVID-19). Using a target-based selection approach, we developed oligonucleotide aptamers containing a conserved sequence motif that specifically targets S/RBD. Synthetic aptamers had high binding affinity for S/RBD-coated virus mimics (K D≈7 nM) and also blocked interaction of S/RBD with ACE2 receptors (IC50≈5 nM). Importantly, aptamers were able to neutralize S protein-expressing viral particles and prevent host cell infection, suggesting a promising COVID-19 therapy strategy.

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