Oligonucleotide-based strategies for capture, detection, adaptation and sequencing of TRNA using nanopore technology
By using a sequencing library preparation method, 3′ and 5′ splice oligonucleotides are hybridized with tRNA, combined with DNA ligase and nanopore direct sequencing, which solves the problem of difficulty in quantifying and detecting modifications in existing tRNA sequencing technologies, and achieves accurate quantification and detection of tRNA abundance and modifications.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- NORTHEASTERN UNIV (US)
- Filing Date
- 2024-10-31
- Publication Date
- 2026-06-09
AI Technical Summary
Existing tRNA sequencing methods are difficult to accurately quantify and monitor its modification dynamics, and cannot simultaneously detect and quantify tRNA abundance and modification.
The sequencing library preparation method was used, 3′ and 5′ splice oligonucleotides were hybridized with tRNA, and the product was formed by DNA ligase. Reverse transcription and direct nanopore sequencing were performed, and ion current analysis was performed using longer adaptor DNA oligonucleotides.
It enables direct sequencing and modification detection of tRNA, improves quantification capabilities, and allows for the simultaneous detection of tRNA abundance and modification, thereby enhancing the accuracy of ion current analysis.
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Abstract
Citation Information
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