Application of r18-7aa polypeptide modified by octadecylation and its derivative polypeptide
A technology of octadecyl and polypeptide, which is applied in the field of preparation of antithrombotic drugs, can solve problems such as increased bleeding risk, neutropenia, and weakened drug efficacy, and achieve the effect of inhibiting platelet aggregation
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Embodiment 1
[0071] platelet aggregation inhibition test
[0072] Healthy human platelets were diluted with plasma to 2.5x10^8 / mL, 300 μL of diluted platelets were taken, and 10 μM, 30 μM and 100 μM of myrR18-7AA polypeptide were added respectively. After incubation at 37°C for 5 minutes, 30 μM of ADP and 2.25 μg / mL of Collagen induced platelet aggregation, and the aggregation curve within 5 minutes was drawn on a platelet aggregometer. Wash the platelets with bench-top solution, and finally dilute the platelets to 2.5x10^8 / mL with bench-top solution B, take 300 μL of washed platelets, add 0.21 μM, 0.63 μM, 1.85 μM and 5.56 μM myrR18 polypeptides, and incubate at 37 °C After 5 minutes, add 2.25 μg / mL collagen to induce platelet aggregation; add 1.85 μM, 5.55 μM, 16.67 μM, 50 μM and 150 μM myrR18 polypeptide respectively, and after incubation at 37°C for 5 minutes, add 0.18 U / mL collagen to induce platelet aggregation; Add 0.1 μM, 0.3 μM and 1 μM myrR18-7AA polypeptide respectively, incuba...
Embodiment 2
[0094] The co-localization of the octadecylated modified R18-7AA polypeptide with 14-3-3ζ;
[0095] Take the concentration as 1×10 4 / mL platelets were added with FITC-myrR18-7AA polypeptide (30 μM, amino acid sequence Myristoylated-SWLDLEA), and FITC-labeled myrR18-7AA disordered polypeptide (FITC-myrR18-7AAscr) was used as a negative control. After mixing, place in a 37°C incubator and incubate for 10 minutes. Add 1 mg / mL fibrinogen to the 12-well plate, air-dry for 2 hours, add the incubated platelets, add thrombin (0.12U / mL), mix well, place in an incubator, incubate at 37°C for 40 minutes, and remove the 12 wells platelet mixture in the plate, add PBS to remove the platelets that are not combined with fibrinogen and adhere to the wall, add 4% paraformaldehyde to fix, after 10min, remove the paraformaldehyde, wash with PBS three times, each After 5 minutes, use 0.3% Triton X-100 solution dissolved in PBS to rupture the membrane, remove after 10 minutes, add PBS to wash t...
Embodiment 3
[0098] The effect of myrR18-7AA polypeptide on the related proteins (c-Src protein, 14-3-3ζ, AKT protein) of integrin outside-in signaling pathway;
[0099] (1) Washed platelets were activated by collagen (1 μg / mL) using a platelet aggregator, and myrR18-7AA polypeptides of different concentrations (0 μM, 0.5 μM, 2.5 μM, 12.5 μM) were added to inhibit the activation of platelets. Platelet samples After obtaining, fully lyse;
[0100] (2) Take 20 μL of Dynabeads Protein A, absorb the magnetic beads with a magnetic stand, remove the solution, add 200 μL of PBS solution with 0.02% Tween-20, wash twice, add 2 μL of β3 protein antibody, and incubate at room temperature for 10 minutes.
[0101] (3) Adsorb the magnetic beads with a magnetic stand, remove the solution, centrifuge at 10,000 g for 5 min after the platelet sample is fully lysed, take the supernatant and add it to the magnetic beads, and incubate at room temperature for 10-30 min (adjust the incubation time according to t...
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