Nucleic acid aptamer specifically binding to arabidopsis cop1 protein and preparation method thereof
Through one-step screening technology and binding site optimization, the nucleic acid aptamers Lib2-11 and Lib2-11c with high affinity and high specificity binding to Arabidopsis COP1 protein were prepared, which solved the time-consuming, complex and costly problems of traditional SELEX screening technology, and realized rapid and low-cost screening and application in synthetic biology.
Patent Information
- Application Number
- CN202510113870.8
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2025-01-24
- Publication Date
- 2025-10-21
- Estimated Expiration
- 2045-01-24
AI Technical Summary
Traditional SELEX screening technology is time-consuming, complex, costly, and not widely applicable. Non-specific binding and PCR amplification deviation are prone to occur during the screening process, which increases the uncertainty of aptamer screening results and makes it difficult to efficiently screen nucleic acid aptamers with high affinity and specific binding to Arabidopsis COP1 protein.
One-step screening technology was used in combination with Arabidopsis COP1 protein. By predicting the binding site and performing truncation optimization, the nucleic acid aptamer Lib2-11 and its truncated sequence Lib2-11c were prepared. They were analyzed using ELONA and gel retardation experiments to achieve rapid and low-cost specific binding.
It achieves high-affinity and high-specificity recognition of Arabidopsis COP1 protein, simplifies the screening process, reduces costs, and improves screening efficiency, making it suitable for the application of synthetic gene circuits and biosensors.
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Abstract
Citation Information
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