Short peptide suppressing growth of cancer cell and uses thereof
A cancer cell, short peptide technology, applied in the field of biotechnology and medicine, can solve the problems of pain, death, damage to normal cells of patients, etc., and achieve the effect of solving serious injuries
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[0018] The preparation method of the short peptide adopts the chemical synthesis method, that is, the solid-phase peptide synthesis method which is well known in the art and has been very mature, and can adopt either the Boc method or the Fmoc method. The specific method is to couple the protected amino acids to an inert solid support one by one, and then use a strong acid to cleave the peptide chain from the support and remove the side chain protection at the same time.
[0019] The amino acid main sequence of the short peptide is the main sequence with fixed amino acid positions, and the corresponding amino acids are arranged in the spaced positions. At the position of J in , no matter which one of them is selected, the short peptide still has its original biological activity, that is, inhibiting the growth of malignant tumor cells. Similarly, the amino acids at the positions represented by B and O also have such properties. .
[0020] Nucleotides are prepared by synthetic ...
Embodiment 1
[0038] Test for inhibiting liver cancer cells (synthesis of short peptides involved in the present invention: Lys-Leu-Pro-Ser-Ser-Ala-Lys or Lys-Leu-Pro-Ser-Ala-Ala-Lys)
[0039] Human hepatoma cell line Bel-7402 cells were cultured in RPMI 1640 medium containing 10% newborn bovine serum at 5 × 10 5 The cell density per well was planted into a 96-well cell plate. After 24 hours, the short peptides involved in the present invention were added to the cell culture plate according to different concentrations. An equal volume of PBS was used as a control group. After 24 hours, a cell counting plate was used. Count, compare the administration group and the control group, and obtain the inhibition rate of liver cancer cells. like figure 1 As shown in the photos taken under the microscope 24 hours after the short peptide and human liver cancer cells involved in the present invention act together, the cells in the administration group Test can obviously observe a significant inhibitor...
Embodiment 2
[0041] Inhibition of acute myeloid leukemia (M 2 ) (synthesis of the short peptide derivatives involved in the present invention, modified with a phosphate group at serine: Thr-Leu-Pro-Serp-Ala-Ala-Lys)
[0042] The human acute myeloid leukemia cell line HL60 cells were cultured in RPMI 1640 medium containing 10% newborn bovine serum at 10 6 After the cell density per well was planted into a 24-well cell plate, the short peptides involved in the present invention were immediately added to the cell culture plate according to different concentrations, and an equal volume of PBS was used as the control group. The existing clinical drug As 2 O 3 As a positive control, after 24 hours, after flow cytometry (FACS), the experimental results are as follows figure 2 shown, where the upper right 59.32% represents the number of dead cells and 38.91% represents the number of early apoptotic cells, the total effective rate of cells being inhibited exceeds 98%.
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