反式激活crRNA
化学
信使核糖核酸
计算生物学
灵敏度(控制系统)
信号(编程语言)
清脆的
小分子
细胞生物学
纳米技术
过程(计算)
作者
M. He,Jinhua Chen,Murilege Chao,Feifan Yin,Han Pan,Qiufeng Wang,Wenting Cheng,Zhongyun Wang,Yang Xiang
标识
DOI:10.1021/acs.analchem.5c06932
摘要
mRNA vaccines, as a new form of vaccine, are gradually revealing their potential in the field of tumor treatment. With the development of mRNA vaccines, monitoring their levels has become particularly important. In this work, a novel and innovative strategy was proposed for the first time, which directly used the target as crRNA and simultaneously triggered an entropy-driven split Cas12a system for triple signal amplification for the high-sensitivity detection of mRNA vaccines. This study broke the traditional full-length crRNA and innovatively designed a split crRNA structure, directly using the target mRNA as the variable sequence of the crRNA. This design avoided the need for additional introduction of variable sequences, thereby eliminating nonspecific signal leakage and multicomponent interference from the source. At the same time, the target molecule served as the initiating chain for the EDC reaction, allowing the split Cas12a system to be coupled with the entire entropy-driven reaction process, achieving efficient collaboration and triple signal amplification and significantly improving the detection sensitivity and specificity. Moreover, the entire detection process required only one reaction step, which was simple, fast, and efficient. The aim was to provide strategies for screening and pharmacokinetic studies of mRNA vaccines.
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