Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Center for Immunotherapy Research, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Angew Chem Int Ed Engl. 2021 Apr 26;60(18):10273-10278. doi: 10.1002/anie.202100345. Epub 2021 Mar 22.
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 ≈7 nM) and also blocked interaction of S/RBD with ACE2 receptors (IC ≈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.
严重急性呼吸综合征冠状病毒 2 刺突(S)蛋白的受体结合域(RBD)在介导病毒感染的第一步中起着核心作用,导致疾病: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 是阻止和中和治疗以预防和治疗 2019 年冠状病毒病(COVID-19)的理想靶标。我们使用基于靶标的选择方法,开发了含有保守序列基序的寡核苷酸适体,该基序特异性靶向 S/RBD。合成适体对 S/RBD 包被的病毒模拟物具有高结合亲和力(K≈7 nM),并且还阻断了 S/RBD 与 ACE2 受体的相互作用(IC≈5 nM)。重要的是,适体能中和表达 S 蛋白的病毒颗粒并防止宿主细胞感染,这表明这是一种有前途的 COVID-19 治疗策略。