A benzisoselenazol derivative, its preparation method and application in preparing RNA fluorescent probe
By covalently linking the benzoselenazole core with the julonidine unit conjugated olefin, the constructed benzoselenazole derivative overcomes the shortcomings of existing RNA fluorescent probes, achieving highly selective recognition and binding of RNA, and is suitable for real-time, dynamic fluorescence imaging detection of RNA.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- GUANGDONG UNIV OF TECH
- Filing Date
- 2026-05-06
- Publication Date
- 2026-06-02
AI Technical Summary
Existing RNA fluorescent probes suffer from low fluorescence quantum yield, significant photobleaching, weak cell membrane penetration, insufficient intracellular enrichment efficiency, poor biocompatibility, and insufficient specific binding ability to RNA, making it difficult to meet the needs of the biomedical field for precise RNA tracing and real-time detection.
A benzoselenazole derivative was designed, in which the benzoselenazole core and the julonidine unit were covalently linked through a conjugated olefin to form a fluorescently activated probe. This probe targets and binds to RNA using electrostatic and π-π intercalation interactions, thereby enhancing molecular binding affinity and fluorescence response. By rigidifying the molecular conformation to inhibit intramolecular rotation, the probe achieves specific activation of the fluorescence signal.
It achieves highly selective recognition and binding of RNA, with high signal-to-noise ratio and excellent fluorescence photostable stability. It is suitable for real-time, dynamic fluorescence imaging detection of RNA in live cells and fixed cell systems, and can realize in-situ visualization and tracing of RNA subcellular distribution and content changes.
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