Seaweed-derived short peptide capable of inhibiting inflammations of digestive tract and application thereof
A digestive tract, short peptide technology, applied in the field of biotechnology and medicine, can solve problems such as difficult to cure, achieve excellent efficacy, no toxic side effects
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[0033] The preparation method of the short peptide adopts a chemical synthesis method, that is, a very mature solid-phase peptide synthesis method well known in the art, and either the Boc method or the Fmoc method can be used. The specific method is to couple the protected amino acids to the inert solid phase carrier one by one, and then use strong acid to cleave the peptide chain from the carrier, and remove the amino acid sequence of the side chain protection short peptide, Ile-Pro-Asp-Asp-Val -Ala or Pro-Asp-Asp-Val-Ala or Ile-Pro-Asp-Asp-Val or Leu-Pro-Asp-Asp-Val-Ala or Val-Pro-Asp-Asp-Val-Ala or Ile-Ser -Asp-Asp-Val-Ala or Val-Ser-Asp-Asp-Val-Ala or Leu-Ser-Asp-Asp-Val-Ala or Ile-Pro-Glu-Asp-Val-Gly or Ile-Pro-Glu -Asn-Leu-Ala or Ile-Pro-Gln-Asp-Ile-Gly as the main sequence, truncated from any position into a short peptide consisting of 3 or 4 or 5 amino acids with the same biological activity as the short peptide Fragments, short peptide analogs, short peptide derivat...
specific Embodiment approach
[0050] The short peptides of the present invention and their analogs, derivatives and fragments (P1~P11, P1 analogs, P1 derivatives (modified with phosphate groups), and fragments of P1) are chemically synthesized by the solid-phase Fmoc method, and purified by HPLC , with a purity of more than 97%, the following animal experiments were carried out.
[0051] Among them, P1 is Ile-Pro-Asp-Asp-Val-Ala, P2 is Pro-Asp-Asp-Val-Ala, P3 is Ile-Pro-Asp-Asp-Val, P4 is Leu-Pro-Asp-Asp- Val-Ala, P5 is Val-Pro-Asp-Asp-Val-Ala, P6 is Ile-Ser-Asp-Asp-Val-Ala, P7 is Val-Ser-Asp-Asp-Val-Ala, P8 is Leu- Ser-Asp-Asp-Val-Ala, P9 is Ile-Pro-Glu-Asp-Val-Gly, P10 is Ile-Pro-Glu-Asn-Leu-Ala, P11 is Ile-Pro-Gln-Asp-Ile- Gly; P1 analogue is Ile-Pro-Asp-Asp-Val-Lys, P1 derivative is Ile-Pro-Asp-Asp-Val p -Ala, the fragment of P1 is Ile-Pro-Asp-Asp.
Embodiment 1
[0052] Example 1 The experiment of seaweed short peptide inhibiting the effect of intestinal inflammation on the weight change of mice
[0053] The mice in this experiment were divided into 15 groups, with 6 mice in each group. They were given drinking water for 7 days to adapt to the environment, and then 2.5% DSS solution for 5 days to establish an acute intestinal inflammation model, and then replaced with tap water for small Rats drank ad libitum. From the first day of the experiment, each mouse in each group was given the short peptide series involved in the present invention, and at the same time every day, each group of mice was gavaged with a short peptide of 1 mg / mL, and the amount of gavage was 200 μL. The comparison of the results of the negative control group verifies the biological activity of the bioactive peptides in the treatment of intestinal inflammation. The mice that have established the model will suffer from loss of appetite or cannot eat normally due to ...
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