适体
指数富集配体系统进化
寡核苷酸
SELEX适体技术
冠状病毒
DNA
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
生物
计算生物学
体外
核酸
血浆蛋白结合
绑定域
化学
病毒学
结合位点
分子生物学
2019年冠状病毒病(COVID-19)
细胞生物学
生物化学
核糖核酸
基因
医学
疾病
病理
传染病(医学专业)
作者
Yongjun Chen,Xuefeng Yang,Jian Liu,Dandan Zhang,Jun He,Liang Tang,Jianming Li,Qin Xiang
标识
DOI:10.1080/15257770.2022.2109170
摘要
Nucleic acid aptamers are developed from a pool of random oligonucleotide libraries with an in vitro selection through systematic evolution of ligands via exponential enrichment (SELEX) process, which are capable of specific and high-affinity molecular binding against targets. The receptor-binding domain (RBD) of spike protein from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is involved in the early stages of viral infection, is a promising target for aptamer selection. Currently, there are no effective approaches to prevent virus from spreading. In this study, a new ssDNA aptamer RBD/S-A1 binding to the RBD of spike protein from SARS-CoV-2 with high affinity (Kd=1.74 ± 0.2 nM) and low cross-binding activity was selected and evaluated. Although aptamers targeting the RBD of spike protein from SARS-CoV-2 have been described in a handful of previous studies, the RBD/S-A1 aptamer identified in this work may be considered as a potential supplementation for the current diagnosis and research of coronavirus SARS-CoV-2.
科研通智能强力驱动
Strongly Powered by AbleSci AI