Construction and expression for tumor immunity synergistic carrier pBVIM
A carrier and tumor technology, applied in the fields of genetic engineering and immunology, to avoid degradation, simple and easy process, and increase translocation
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example 1
[0037] Example 1, construction of expression vector pBVIM
[0038] 1. Determine the molecular order of immune potentiating elements
[0039] In the present invention, active small molecules such as SLC, PADRE, penetrating peptide, phagocytic release agent and cationic peptide are selected as the backbone gene of the carrier, and at the same time, multiple cloning restriction sites are inserted into the gene sequence combination, and the linked gene is inserted into the carrier pBV220 A schematic diagram of the structure (see Figure 1).
[0040] 2. Gene synthesis of vector immune potentiating elements
[0041] The tetrapeptide sequence is placed at the starting position of the N-terminal of the vector for MARV, which can improve the expression ability of the vector itself. The gene of SLC was retrieved from GENEBANK on the Internet. The signal peptide sequence of 69 bp was removed, and the mature peptide sequence of 333 bp was selected as the selected gene. The multiple cloni...
example 2
[0059] Example 2. The expression of the antigen gene after it is inserted into the vector
[0060] 1. Obtain antigen gene by PCR method
[0061] In order to verify whether the designed vector of the present invention can efficiently express genes, we selected an antigen gene expressed in our laboratory to insert into the vector pBVIM to verify the expression. The gene is a core streptavidin gene with a full length of 387bp. Design primers with Xho I and Xba I restriction sites at both ends:
[0062] F1 GGT GGT GGA TCT GGTGCTGCTGAAG
[0063] R1 ACC TCC ACC ACT GGAGGCGGCGGAC
[0064] The PCR amplification system is: 10×Buffer 5μl, primers (20pmol / μl) R1, F1 1μl each, 4dNTPs (2.5mM) 4μl, Taq DNA polymerase (5U / μl) 0.5μl, add water to 50μl. (Taq DNA polymerase, Buffer, and dNTPs were all purchased from Tacara Biotechnology Co., Ltd.). PCR amplification reaction: 94°C for 1 minute, 55°C for 1 minute, 72°C for 1 minute, a total of 30 cycles.
[0065] The PCR product was purifie...
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