Purpose of polyether compound in medicine preparation and anti-tumor medicine screening method
A technology for preparing drugs and compounds, which is applied in the field of biomedicine and can solve problems such as the use of polyether antibiotics to be studied
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Embodiment 1
[0041] The preparation method of embodiment 1 polyether compound
[0042] One Streptomyces nanchangensis subtype, two Streptomyces hygroscopicus subtypes and one Streptomyces endus subtype Streptomyces were inoculated on the SFM plate, and cultured for about three to four days. When colonies are formed in the SFM medium, pick a single colony and culture it in the seed medium for about three to four days, and inoculate it into the fermentation medium according to 1% amount (the composition of the fermentation medium is 30g / L of soluble starch, yellow Bean cake powder 10g / L, yeast extract 2.5g / L, CaCO 3 3g / L, pH 7.2). Culture conditions: 30 degrees, 220 rotation speed, culture for 7 to 8 days.
[0043] When the culture reaches the 7th or 8th day, collect the fermentation broth and centrifuge at a high speed to separate the supernatant from the mycelium, add an equal amount of acetone to the mycelium to destroy the bacteria, ultrasonicate for 20 minutes, spin evaporate acetone...
Embodiment 2
[0054] Example 2 Research on J1001-2 Sodium Salt by Proteomics and Phosphoproteomics
[0055] (1) Cell culture
[0056] MDA-MB-231 cells (triple-negative breast cancer cells) were cultured with DEME containing 10% fetal bovine serum, 80 μg / m L streptomycin, and 80 U / m L penicillin at 37°C and 5% CO 2 Routine cultivation in an incubator. When the cells are about 90% full, add the drug J1001-2 sodium salt. In the protein group experiment, 3 administration groups (administration concentration of 2 μM) were set up, respectively 24h, 48h, 72h and a blank group (no drug addition). In the phosphorylated protein group experiment, two administration groups (administration concentration of 3 μM) were set up for 6h, 12h and a blank group (no drug addition).
[0057] (2) Experimental methods of proteomics
[0058] 1) Proteome sample preparation
[0059] Collect the cells of the blank group and the administration group, transfer to a 1.5mL centrifuge tube, centrifuge at 2500rpm at 4°C...
Embodiment 3
[0080] Example 3 Study on the Targets of Polyether Compounds for Inhibiting Tumors
[0081] 1. Experimental method—western blotting experiment
[0082] Protein gel concentration: 8% precast gel, 10% precast gel, 12% precast gel, 4-20% precast gel (from GenScript)
[0083] Set up the administration group as shown in the figure below, collect cells 16 hours after administration, digest with 0.125% trypsin, wash twice with PBS, centrifuge, add 400L of RIPA per 10cm dish cell volume (in which protease inhibitors and phosphorylation are added to RIPA Protease inhibitors) lyse the cells on ice for 1-2 hours, and centrifuge at 4 degrees at high speed (12000rmp×10min). Aspirate the supernatant as the protein.
[0084] Protein loading amount: (uniform loading amount 25ng) (MDA-MB-231 cells)
[0085] BCA determination of protein concentration standard curve such as Image 6 shown.
[0086] Calculate the concentration (in μg / mL) through the standard curve as follows:
[0087] ...
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