脱氧核酶
劈开
DNA
核酸内切酶
核糖核酸
化学
核苷酸
识别序列
生物化学
劈理(地质)
计算生物学
酶
分子生物学
限制性酶
信使核糖核酸
体外
核酶
A-DNA
生物
结合位点
核酸结构
立体化学
内切酶
细胞生物学
A站点
核酸
活动站点
碱基对
蛋白质-DNA相互作用
作者
Shusen Xiao,Yangyang Chang,Jia Pan,Xiaoqian Li,Li Xia,Xiaozheng Li,Hong Yuan,Jiuxing Li,Zijie Zhang,Meng Liu
标识
DOI:10.1002/anie.202513587
摘要
Abstract We report an RNA‐cleaving DNAzyme (RCD), RCD‐I4T3, discovered through in vitro selection, that can specifically recognize an inosine‐modified site in RNA and cleave at a remote site (eight nucleotides downstream of the inosine). RCD‐I4T3 represents the first DNAzyme with spatially separated domains for target recognition and catalytic cleavage, functionally analogous to Type IIS restriction endonucleases and endonuclease V, which is not previously observed in DNA catalysts. The RCD‐I4T3 serves as a potent RNA‐cleaving tool, exhibiting an observed rate constant ( k obs ) of 1.9 × 10 −2 min −1 for inosine‐modified RNA, and successfully targeting natural inosine‐containing mRNA fragments with high specificity. This modular architecture minimizes the off‐target activity through stringent two‐step validation (i.e., recognition and cleavage) and enables independent functional optimization. The unique structural and mechanistic features of RCD‐I4T3 expand the functional repertoire of DNAzymes for biological applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI