Collateral nuclease activity of TnpB triggered by high temperature enables fast and sensitive nucleic acid detection

被引:0
|
作者
Xu, Ying [1 ]
Yin, Wen [2 ]
Cheng, Yibin [2 ]
Zeng, Wei [2 ]
Li, Wenqiang [2 ]
Chen, Wanping [2 ]
Wang, Fei [2 ]
Peng, Nan [1 ]
Ma, Lixin [2 ]
Liu, Tao [2 ]
机构
[1] Huazhong Agr Univ, Coll Life Sci & Technol, State Key Lab Agr Microbiol, Hubei Hongshan Lab, Wuhan, Peoples R China
[2] Hubei Univ, Sch Life Sci, State Key Lab Biocatalysis & Enzyme Engn, Hubei Key Lab Ind Biotechnol, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA;
D O I
10.1038/s42003-024-07123-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
TnpB proteins encoded in the IS200/IS605 family are RNA-guided endonuclease which can be harnessed in genome editing. However, the collateral nuclease activity of TnpB remains poorly understood, which limits the development of TnpB-based diagnostic tools. Here we showed that TnpB from a thermophilic archaeon exhibits enhanced collateral ssDNA cleavage activity (trans-cleavage) activated by high temperature. Mutations either in the TAM or seed sequences of the target DNA impair the trans-cleavage activity, which indicates its potential to be employed in molecular diagnostic. Importantly, by optimizing the length and the sequences of the collateral substrates, we have developed a new nucleic acid detection method based on TnpB with a sensitivity of 29 cp mu l-1 in 30 min, which we name it TESD (TnpB Enable fast and Sensitive Detection). In summary, our findings illustrate the collateral nuclease activity of a TnpB from thermophiles and provide a novel platform for molecular diagnostics. TnpB protein from a thermophilic archaea has collateral ssDNA cleavage activity activated by high temperature that has been employed in developing a new fast and sensitive TnpB-based nucleic acid detection tool (TESD).
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页数:8
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