Purification process of oas1-cas12a rec fusion protein
By optimizing the matching of the encoding gene of the OAS1-Cas12aREC fusion protein with the E. coli translation system and optimizing the purification reagents, the problems of insufficient yield and purity in the existing technology were solved, and efficient and stable purification results were achieved.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- HAINAN UNIV
- Filing Date
- 2026-02-05
- Publication Date
- 2026-06-02
AI Technical Summary
Existing technologies are insufficient to effectively improve the purification yield and purity of OAS1-Cas12aREC fusion protein, and their stability is inadequate during expression and purification.
By optimizing the coding gene of the OAS1-Cas12aREC fusion protein to match the translation system of E. coli, the translation bottleneck was eliminated. The composition of reagents in the purification process was also optimized, including the components of bacterial lysis buffer, affinity equilibration buffer and affinity elution buffer. The protein was purified using ultrasonic disruption and affinity chromatography techniques.
It improved the yield and purity of the OAS1-Cas12aREC fusion protein, enhanced its stability during expression and purification, prevented protein oxidation and denaturation, and achieved efficient purification results.
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