Polypeptide inhibitor for APC/Asef interaction and application thereof
A peptide inhibitor, -SO2RA1 technology, applied in the field of peptides, can solve the problems of APC full length, difficult transfection, limited application, etc.
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Embodiment 1
[0059] Example 1 Solid phase synthesis, cleavage, purification and identification of polypeptide 1
[0060] 1.1 Solid phase synthesis of polypeptide 1
[0061] The present invention utilizes a polypeptide synthesizer to synthesize polypeptide 1 (Ac-GEALE-NH 2 ): With DMF as the solvent, the concentration of various α-amino amino acid solutions protected by Fmoc is 0.25mol / L, the concentration of HBTU solution and HOBt solution is 0.33mol / L, the concentration of piperidine solution is 200ml / L, and the concentration of DIEA solution The concentration is 174.2ml / L.
[0062] 1.1.1 Activated resin
[0063] Take 1g of Fmoc (fluorenebenzyloxycarbonyl)-protected butyramide resin and put it into the reactor, add an appropriate amount of dichloromethane to expand the resin, remove excess dichloromethane in the reactor by suction filtration, and put the expanded resin back into the reactor. Add 6.00mL of N,N-dimethylformamide solution containing 20% piperidine and shake for 5 minute...
Embodiment 2
[0070] Example 2 Prepare the polypeptide 2Ac-GA-Cycloleucine-LA-NH according to the same method as in Example 1 2 , solid purity greater than 98%, ESI: 499.5 [M-H] - ;
Embodiment 3
[0071] Example 3 Prepare the polypeptide 3Ac-GE-HomoPro-LA-NH according to the same method as in Example 1 2 , solid purity greater than 98%, ESI:539.64[M-H] - ;
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