Fukuda Masatora, Tanabe Yukiko, Morii Takashi
Institute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan.
Nucleic Acids Symp Ser (Oxf). 2005(49):355-6. doi: 10.1093/nass/49.1.355.
We describe here stepwise functionalization strategies of ribonucleopeptide complexes to receptors and sensors. A structurally well-defined complex of RNA and peptide (ribonucleopeptide: RNP) was constructed by a structure-based design. The first step optimizes an ATP-binding characteristic of an RNP receptor based on an in vitro selection of an RNP library generated by introducing randomized nucleotide sequences in the RNA subunit. In the second step, the RNP receptor from the first step was functionalized to an RNP receptor for nicotinamide adenine dinucleotide (NAD+) or to ATP sensors by using respective modifications of the peptide subunit.
我们在此描述核糖核肽复合物与受体和传感器的逐步功能化策略。通过基于结构的设计构建了一种结构明确的RNA与肽的复合物(核糖核肽:RNP)。第一步基于对通过在RNA亚基中引入随机核苷酸序列生成的RNP文库进行体外筛选,优化RNP受体的ATP结合特性。第二步,通过对肽亚基进行相应修饰,将第一步得到的RNP受体功能化为烟酰胺腺嘌呤二核苷酸(NAD+)的RNP受体或ATP传感器。