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

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 μl<sup>-1</sup> 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.

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Publication Details

Journal
Communications Biology
Published
2024-11-20
DOI
https://doi.org/10.1038/s42003-024-07123-3
Citations
2
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
0.47

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article

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

Wen Yin, Wei Zeng, Nan Peng, Tao Liu et al.
2 citations
Communications Biology
CRISPR and Genetic Engineering
0.47
article

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

Wen Yin, Wei Zeng, Nan Peng, Tao Liu, Wenqiang Li, Fei Wang, Wan‐Ping Chen, Ying Xu, Yibin Cheng, Lixin Ma
article en
2 citations

Abstract

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 μl<sup>-1</sup> 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.

Communications BiologyVol. 7(1)
Huazhong Agricultural University (CN), Hubei University (CN)
National Natural Science Foundation of China, National Postdoctoral Program for Innovative Talents
Openalex Percentile: Top 34%
CRISPR and Genetic Engineering
0.47
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Collateral nuclease activity of TnpB triggered by high temperature enables fast and sensitive nucleic acid detection — Wen Yin, Wei Zeng, et al. · Communications Biology (2024) | TGRS Research Map | TGRS