Nanoparticle-rhACE-2 compound for blocking coronavirus from infecting target cells, preparation method and application of nanoparticle-rhACE-2 compound
A -rhace-2, nanoparticle technology, applied in the field of medicine, to achieve strong anti-degradation ability, high safety, and the effect of inhibiting virus infection
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Embodiment 1
[0037] Embodiment 1 plasmid construction
[0038] Artificially synthesized human angiotensin-converting enzyme 2 (GenBank: AB046569.1) corresponding to the nucleic acid sequence from 18 to 740 amino acids, expressed His tag protein at the C-terminus for purification, and expressed Avi tag behind the His tag for Biotin labeling. The specific steps are as follows: 100 ng of PCR product; 100 ng of Topo carrier; 1 ml of BP clonase; TEbuffer to 5 μl; Then, the above ligation product was transformed into Escherichia coli competent cells: the specific steps were: the volume of competent cells was 100 μl, adding 2 μl of the above reaction product, incubating on ice for 30 min, and heat shocking at 42°C for 90 sec. Incubate on ice for 2 min. Add 250 μl of SOC medium. Shake the bacteria at 225 rpm for 1 h at 37°C, and spread 100 μl of the product onto an LB plate. Incubate overnight at 37°C. Pick cloned colonies for PCR identification, and shake positive clones for plasmid extracti...
Embodiment 2
[0040] Example 2 Packaging produces pseudoviruses of the new coronavirus and protein purification
[0041] The day before will be about 4*10 7Cells were plated in a 10cm cell culture dish and prepared for toxin production. Use lipofectamine-2000 to transfect the plasmid packaging virus. According to the instructions, the vector expression plasmid (pLV-CMV-Luciferase), integration plasmid (pSPAX2) and envelope plasmid (PRP-CMV-human-beta-globin-intron-S) were added to 4ug :2ug:1ug was added to 1ml Opti-MEM, and 12ul lipofectamine-2000 was added to another tube of 1ml Opti-MEM at the same time, the two were mixed and left at room temperature for 15 minutes, then added dropwise to the prepared 293T cells After 8 hours, change the fresh medium, collect the supernatant after 48 hours, centrifuge at 3000g for 30 minutes, discard the precipitate, the supernatant is the virus solution, and store at -80°C. stand-by. ACE-2 purification: the expression vector pRP-EGFP-hACE-2[18-740aa]...
Embodiment 3
[0042] Example 3 Detection of the toxicity of different concentrations of nanoparticles and soluble ACE-2 to cells
[0043] The streptavidin-coated nanoparticles were purchased from sigma company, invitrogen company, and Xi'an Ruixi Biomaterials Co., Ltd., and the streptavidin-modified soluble nanomicelles were prepared by our laboratory. The specific steps were as follows: firstly, Commercially purchased streptavidin-labeled distearoylphosphatidylethanolamine-polyethylene glycol 2000 (DSPE-PEG2000-streptavidin) was placed at room temperature for 30 minutes, then 5 mg was weighed and dissolved in 1 ml DMSO until fully dissolved Finally, add it dropwise to 2ml of ultrapure water, stir while adding, stir evenly, put it in a 500WM dialysis bag for dialysis for 6 hours, then take out the dialysis bag, and then use the probe to sonicate for 1 minute and 1 minute, the product is Streptavidin-modified nanomicelles, stored at 4°C until use. Spread 1X104 wells of 293T cells into a 96-...
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