核糖核酸
化学
核酶
鸟嘌呤
磷酸二酯键
磷酰胺
碱基对
连接酶核酶
核酸结构
RNA编辑
信号识别粒子RNA
突变
核苷酸
立体化学
寡核苷酸
生物化学
DNA
突变体
基因
作者
Raphael Bereiter,Eva Renard,Kathrin Breuker,Christoph Kreutz,Eric Ennifar,Ronald Micura
摘要
Atomic mutagenesis is the key to advance our understanding of RNA recognition and RNA catalysis. To this end, deazanucleosides are utilized to evaluate the participation of specific atoms in these processes. One of the remaining challenges is access to RNA-containing 1-deazaguanosine (c1G). Here, we present the synthesis of this nucleoside and its phosphoramidite, allowing first time access to c1G-modified RNA. Thermodynamic analyses revealed the base pairing parameters for c1G-modified RNA. Furthermore, by NMR spectroscopy, a c1G-triggered switch of Watson-Crick into Hoogsteen pairing in HIV-2 TAR RNA was identified. Additionally, using X-ray structure analysis, a guanine–phosphate backbone interaction affecting RNA fold stability was characterized, and finally, the critical impact of an active-site guanine in twister ribozyme on the phosphodiester cleavage was revealed. Taken together, our study lays the synthetic basis for c1G-modified RNA and demonstrates the power of the completed deazanucleoside toolbox for RNA atomic mutagenesis needed to achieve in-depth understanding of RNA recognition and catalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI