Cationic antibacterial peptide modified by dopamine or derivative thereof as well as preparation and application thereof
An antimicrobial peptide and dopamine technology, which is applied in the field of antibacterial biomaterials, can solve the problems of human cytotoxicity and instability of natural antimicrobial peptide protease, etc., and achieve good adhesion performance, high-efficiency broad-spectrum killing effect, good adhesion performance and broad-spectrum The effect of antibacterial function
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Embodiment 1
[0042] The amino acid sequence of the cationic antibacterial peptide is KKFEFEFEFEKK, the structural formula of the antibacterial peptide is KKFE(DA)FE(DA)FE(DA)FE(DA)KK-NH2, and DA is dopamine.
[0043] Note: The C-terminus in the structural formula of the antimicrobial peptide contains -NH2. Those skilled in the art can understand that the carboxyl amidation of the antimicrobial peptide belongs to the conventional treatment method of the antimicrobial peptide. E(DA) indicates that dopamine is modified on the side chain of glutamic acid through an amide bond.
[0044] The preparation method of above-mentioned antimicrobial peptide:
[0045] (1) Weigh 0.3 g of Rink Amide-AM resin to the peptide synthesis device, add dry N,N-dimethylformamide (DMF) and shake for 2 hours to swell the resin. Then, 10 mL of DMF solution containing 20% piperidine (volume fraction) was used to remove the protective group of the resin, and the operation was repeated twice, each lasting 20 minutes....
Embodiment 13 to Embodiment 17
[0056] From Example 13 to Example 17, except that dopamine is replaced by one of α-methyldopamine, norepinephrine, levodopa, α-methyldopa and droxidopa, the parameters used, Condition etc. all keep consistent with embodiment 1.
Embodiment 18
[0058] The antimicrobial peptide prepared in Example 1 was formulated into an aqueous solution with a mass fraction of 2%, and the pH value was adjusted to 2.5 with dilute hydrochloric acid. After 6 hours of irradiation under a 254nm ultraviolet lamp, the above solution undergoes a sol-gel transition to obtain an antimicrobial peptide hydrogel.
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