适体
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
冠状病毒
化学
2019年冠状病毒病(COVID-19)
计算生物学
2019-20冠状病毒爆发
糖蛋白
血浆蛋白结合
竞争性约束
病毒学
结合位点
爆发
受体
分子生物学
生物化学
生物
传染病(医学专业)
医学
疾病
病理
作者
Yanling Song,Jia Song,Xinyu Wei,Mengjiao Huang,Miao Sun,Lin Zhu,Bingqian Lin,Haicong Shen,Zhi Zhu,Chaoyong Yang
标识
DOI:10.1021/acs.analchem.0c01394
摘要
values of the optimized CoV2-RBD-1C and CoV2-RBD-4C aptamers against RBD were 5.8 nM and 19.9 nM, respectively. Simulated interaction modeling, along with competitive experiments, suggests that two aptamers may have partially identical binding sites at ACE2 on SARS-CoV-2 RBD. These aptamers present an opportunity for generating new probes for recognition of SARS-CoV-2 and could provide assistance in the diagnosis and treatment of SARS-CoV-2 while providing a new tool for in-depth study of the mechanisms behind the coronavirus infection.
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