The invention belongs to the technical field of polypeptide
chemical synthesis, and provides a preparation method of mu-conopeptide refined
peptide, which comprises the following steps: S1, sequentially
coupling amino acids containing protecting groups by adopting a
solid-
phase synthesis technology to prepare mu-conopeptide resin, then
cutting the resin and removing the protecting groups of
amino acid side chains to obtain mu-conopeptide resin; the preparation method comprises the following steps of: obtaining a [mu]-conopeptide linear
peptide, namely H-Pyr-Gly-Cys-Cys-Asn-Gly-Pro-Lys-Gly-Cys-Ser-Lys-Trp-Cys-Arg-Asp-His-Ala-Arg-Cys-NH2, and carrying out ultrasonic treatment to obtain the [mu]-conopeptide linear
peptide. S2, dissolving the [mu]-conopeptide linear peptide in a 1-butyl-3-methylimidazolium dihydrogen
phosphate ion solution, adding
sodium sulfate, and carrying out air oxidation
pairing ring formation to obtain [mu]-conopeptide crude peptide; and S3, purifying the [mu]-conopeptide by using an
ultrafiltration method in combination with a
high performance liquid chromatography to obtain the [mu]-conopeptide refined peptide. According to the [mu]-conopeptide cyclization method, expensive reagents are not used, the cost is relatively low, the folding rate of the conopeptide is high in
correctness, and the improved purification method is suitable for large-scale production.