Application of angiogenesis inhibitor polypeptide to preparation of medicine for treating tumor and rheumatoid arthritis
A technology of angiosuppression and tumor drug, applied in the field of disease treatment and angiogenesis inhibitor, can solve the problems of insufficient amount, persistent unrelieved symptoms, repeated symptoms, etc.
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Embodiment 1
[0037] Preparation and Test of Angiogenesis Inhibitor Polypeptide
[0038] The polypeptide is synthesized by solid-phase synthesis, purified by high-performance liquid chromatography, and the molecular weight of the polypeptide is determined by MS, and the purity of the polypeptide is determined by RP-HPLC.
[0039] Polypeptide I, Peptide II, Peptide III and Peptide IV solid-phase synthesis methods use Fmoc-Rink-resin as the starting material, and then use protected amino acids to inoculate each amino acid in turn. After the peptide incorporation is completed, it is fully washed, and then the peptide is cut and post-treated. The crude product of the angiogenesis inhibitor was obtained. The crude product was dissolved, purified twice by preparative high performance liquid phase, and finally concentrated and freeze-dried to obtain the pure product. The method not only ensures the synthesis efficiency, but also improves the purity.
[0040] 1. The steps of receiving peptide are...
Embodiment 2
[0058] Inhibition of several target enzymes by angiogenesis inhibitors.
[0059] Experimental method: Recombinant human matrix metalloproteinase-9 was expressed by Sf9 insect cells. The enzyme was activated with 0.01 μM matrix metalloproteinase-3 active site, and the buffer used was 100 mM Tris / HCl, pH 7.4, 100 mM NaCl, 10 mM CaCl 2 and 0.01% Tween-20. The concentration of matrix metalloproteinase-9 during activation was 92ng / μl (1μM). Enzyme activity is detected by cleaving the fluorescently generated peptide substrate Mca-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH 2 And detect the generated fluorescence value (excitation wavelength = 328nm, detection wavelength = 392nm). All the detection is carried out in 100μl reaction system at 37°C.
[0060] Recombinant human matrix metalloproteinase-8 is detected similarly to -9 and uses the same fluorogenic substrate. The reaction was also carried out in a 100 μl reaction system at 37°C. Add 20 μl of recombinant human matrix metalloproteinas...
Embodiment 3
[0067] Migration Inhibition Test of Human Umbilical Vein Endothelial Cells (HUVEC) by Angiogenesis Inhibitor Peptides
[0068] 10 mg / ml Matrigel (BD Company, USA) was diluted 1:2 with HUVEC-specific medium, spread on the transwell membrane, and air-dried at room temperature. The HUVEC cells cultured to the logarithmic growth phase were digested, collected, counted, and the cell concentration was adjusted to 1×10 5 pieces / ml. The cells were inoculated into the transwell chamber, 100 μl per well, and each group of test liquid was added into the chamber. Add 0.6ml of endothelial cell culture medium containing 5% fetal bovine serum and 1% ECGS to the 24-well plate to stimulate cell migration, in 5% CO 2 , and cultivated at 37°C for 24h. The culture medium in the well was discarded, the cells were fixed, stained, rinsed with clean water, observed under a microscope and selected four fields of view to take pictures and count. Migration inhibition (MI) was calculated according to...
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