Anti-HIV-1 (human immunodeficiency virus 1) gene, application thereof, DC vaccine containing gene and preparation method of vaccine
An HIV-1 and gene technology, applied in the field of genes, can solve the problems of difficult exposure of antigenic epitopes, weak binding site affinity, immune escape of virus mutation, etc. Effect
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Embodiment 1
[0047] Anti-HIV-1 gene, the gene is composed of GM-CSF nucleic acid artificial sequence and gp120-CD4 module in series, and the gp120-CD4 module contains at least one of the following gene fragments;
[0048] (1) gp120(B) nucleic acid artificial sequence, G4S nucleic acid artificial sequence, CD4 nucleic acid artificial sequence;
[0049] (2) gp120(C) nucleic acid artificial sequence, G4S nucleic acid artificial sequence, CD4 nucleic acid artificial sequence;
[0050] (3) gp120 (AE) nucleic acid artificial sequence, G4S nucleic acid artificial sequence, CD4 nucleic acid artificial sequence;
[0051] When the gp120-CD4 module contains two or more gene fragments, the contained gene fragments are concatenated.
[0052] In more detail, the anti-HIV-1 gene of the present invention can be the following gene sequence: GM-CSF-(1), GM-CSF-(2), GM-CSF-(3), GM-CSF-(1) -(2), GM-CSF-(1)-(3), GM-CSF-(2)-(3), GM-CSF-(1)-(2)-(3); can also be GM- CSF-(2)-(1), GM-CSF-(3)-(1), GM-CSF-(3)-(2),...
Embodiment 2
[0056] Purification of HIV-gp120-CD4 gene.
[0057] In more detail, the above steps are:
[0058] The synthetic HIV-gp120-CD4 gene was inserted into the standard vector pUC, so it was called pUC-HIV-gp120-CD4, and pUC-HIV-gp120-CD4 was subjected to Fast Digest AsiSI (purchased from ThermoFisher Company) and FastDigest NotI (purchased from ThermoFisher Company) double enzyme digestion, 37 ° C, enzyme digestion 20min. 100μl enzyme digestion system: 10×buffer: 10μl; DNA 6μg; AsiSI enzyme: 3μl; NotI enzyme: 3μl; deionized water to make up the volume.
[0059] Use agar gel electrophoresis to cut off the agar gel part containing the HIV-gp120-CD4 DNA fragment, and put it in two centrifuge tubes. DNA was extracted from the agar gel using a DNA extraction kit (purchased from ThermoFisher) and concentrated. First, 500 μl DF buffer was added to the above-mentioned centrifuge tube for 10 minutes at 55° C. and shaken every 2-3 minutes until the agar gel was completely dissolved. Inhale...
Embodiment 3
[0061] Preparation of plasmids containing the HIV-gp120-CD4 gene.
[0062] Insert the HIV-gp120-CD4 gene synthesized in Example 2 into the lentiviral expression vector pLent-C-GFP (Invitrogen) NotI-AsiSI site (see figure 2 ).
[0063] In more detail, it is prepared as follows:
[0064] Simultaneously carry out Fast Digest AsiSI (purchased from ThermoFisher Company) and Fast Digest NotI (purchased from ThermoFisher Company) double enzyme digestion of pUC-HIV-gp120-CD4 (prepared in the first step of Example 2) and pLent-C-GFP vector , 37°C, enzyme digestion for 20min. 100μl enzyme digestion system: 10×buffer: 10μl; DNA 6μg; AsiSI enzyme: 3μl; NotI enzyme: 3μl; deionized water to make up the volume. Use agar gel electrophoresis to cut out the agar gel parts containing the HIV-gp120-CD4 DNA fragment and the linearized pLent-C-GFP DNA fragment respectively, and place them in two centrifuge tubes. Use DNA extraction kit (purchased from ThermoFisher Company) to dissolve and conc...
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