Anti-cd138 chimeric antigen receptor, coding gene, recombinant expression vector and its construction method and application
A chimeric antigen receptor, chimeric receptor technology, applied in the direction of carrier, antibody medical component, recombinant DNA technology, etc.
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Embodiment 1
[0079] Example 1 Construction of recombinant lentiviral vector
[0080] 1. Materials
[0081] 1. The lentiviral backbone plasmid pLenti-3G basic, the lentiviral packaging plasmids pPac-GP, pPac-R and the membrane protein plasmid pEnv-G, HEK293T / 17 cells, and homologous recombination enzyme were supplied by Shiao (Shanghai) Biomedical Technology Co., Ltd. supply;
[0082] 2. Primers: According to the principles of primer design, the primers required for amplifying DNA fragments and target sites are designed. The primers are synthesized by Shanghai Biological Company, specifically:
[0083] EF1α-F: 5'-attcaaaattttatcgatgctccggtgcccgtcagt-3' (SEQ ID NO. 26)
[0084] EF1α-R: 5'-TCACGACACCTGAAATGGAAGA-3' (SEQ ID NO.27)
[0085] CD8leader-F: 5'-ggtgtcgtgaggatccgccaccatggccttaccagtgaccgc-3'
[0086] (SEQ ID NO. 28)
[0087] CD8leader-R: 5'-GTGTCATCTGGATGTCCGGCCTGGCGGCGTG-3' (SEQ ID NO.29)
[0088] VL-F: 5'-ccacgccgccaggccggacatccagatgacccagagca-3' (SEQ ID NO.30)
[0089] VL-...
Embodiment 2
[0179] Example 2 Concentration and detection of recombinant lentiviral vector
[0180] Purify the recombinant lentiviral vector by ultracentrifugation;
[0181] (1) Divide the collected supernatant into 50ml centrifuge tubes, centrifuge at 500g room temperature for 10min, and remove cells and large debris;
[0182] (2) Filter the supernatant with a 0.22 μm-0.8 μm filter;
[0183] (3) Take 6 Hitachi 40PA ultracentrifuge tubes, spray 70% ethanol on the surface to sterilize them, put them on a clean table and irradiate them with ultraviolet light for 30 minutes to sterilize them. It can also be sterilized by high temperature and moist heat;
[0184] (4) Aliquot 32ml of the cell supernatant sample processed in step 2 into a centrifuge tube;
[0185] (5) Cover the metal cover, balance the centrifuge tube together with the metal cover, and adjust with 1XPBS to make the weight deviation within 0.02g;
[0186] (6) Place the balanced centrifuge tubes symmetrically in the ultracentr...
Embodiment 3
[0262] Example 3 Functional detection of recombinant lentiviral vectors lvCAR138-CLA, lvCAR138-CLB, lvCAR138-OLC
[0263] 1. Cell-level expression detection of CAR gene:
[0264] (1) After infecting PBMC cells with recombinant lentiviral vectors lvCAR138-CLA, lvCAR138-CLB, and lvCAR138-OLC, collect the cells and use RT-PCR to detect CAR mRNA transcription levels to verify the expression of CAR genes. If the CAR mRNA transcription levels increase, then It shows that the transcription level expression of CAR gene is successful;
[0265] (2) After infecting PBMC cells with recombinant lentiviral vectors lvCAR138-CLA, lvCAR138-CLB, and lvCAR138-OLC, collect the cells and detect the expression level of CAR protein by western blot to verify the expression of CAR gene. If the expression level of CAR protein increases, then It shows that the translation level expression of CAR gene is successful;
[0266] (3) Infect the cells with lvCAR138-CLA, lvCAR138-CLB, lvCAR138-OLC and the con...
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