A kind of tnk-tpa fusion protein with enhanced transport ability through epithelial cells and its application
A technology of fusion protein and epithelial cells, which is applied in the field of genetically engineered recombinant proteins, can solve problems such as difficult to meet needs, and achieve the effects of reduced molecular weight, great flexibility, and weak binding force
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Embodiment 1
[0037] Example 1: Construction and cloning of IgG2 Fc mutant gene
[0038] The human antibody IgG2 Fc fragment encoding gene used in the present invention is obtained by conventional gene cloning techniques, that is, the RNA of normal human peripheral blood leukocytes is extracted, transcribed into cDNA molecules, and then PCR-amplified with specific primers to obtain specific fragments. This fragment was cloned into the pUC18 plasmid to obtain the recombinant plasmid pUCIgG2, and its DNA sequence was confirmed by gene sequencing. It was confirmed by DNA sequencing that the cloned human antibody IgG2 Fc fragment coding gene had 100% homology with the human IgG2 antibody cDNA sequence numbered AK130614.1 in GenBank (GenBank) (such as SEQ ID NO: 1, SEQ ID NO: 2 shown).
[0039] In order to obtain the IgG2 Fc mutant gene, site-directed mutagenesis was performed by partial overlapping gene amplification technique. There are four oligonucleotide primers used in PCR amplification,...
Embodiment 2
[0045] Example 2: Construction of TNK-tPA and IgG2 Fcm fusion coding gene and recombinant expression vector
[0046] In order to construct the fusion coding gene of TNK-tPA and IgG2 Fcm, gene recombination was carried out by overlapping gene amplification technology. 所使用的寡核酸引物共有4条,分别为F3(5’gactctagaccaccatggatgcaatgaagaga3’),R3(5’tgagctgtctcggcggcggaggcctcggtggtggtgggccagcgtacaacagtgctta3’)F4(5’cgaccgggtggtggtggctccggaggcggcggctctgtcgagtgcccaccgtgccca3’),R4(5’taagtcgactcatttacccggagacag3’)。 The F3 primer contains the endonuclease XbaI recognition site (tctaga), the kozak sequence (ccaccatgg) and the start codon (atg), and the R4 primer contains the endonuclease SalI recognition site (gtcgac) and the stop codon. The complementary sequences of the primers R3 and F4 contain a flexible linker coding sequence (ggtggtggtggctccggaggcggcggctct) (shown in SEQ ID NO: 5, SEQ ID NO: 6).
[0047] The operation process is as follows:
[0048] The pCD4mtPA recombinant plasmid contains the co...
Embodiment 3
[0054] Example 3: Expression of pCDTPAFcm and pCD4TPAFc recombinant expression plasmids in CHO cells
[0055] The mammalian cell expression system selected in the present invention is Chinese hamster ovary cells (CHO) deficient in dihydrofolate reductase (dhfr). The recombinant expression vector pCD4 contains an expressible dhfr coding gene. After the plasmid is transfected into CHO (dhfr-) cells, the copy number is greatly increased under the pressure of methotrexate (MTX), and at the same time, it drives the high-efficiency expression of the cloned foreign gene.
[0056] After the recombinant expression plasmids pCDTPAFcm and pCD4TPAFc constructed in Example 2 were purified and endotoxin removed, they were transfected into CHO (dhfr-) cells by liposome method, cultured in selective medium and detected by ELISA, and positive expression of TPA was screened of cell lines. For these positive cell lines, the concentration of MTX in the medium was gradually increased, and the hig...
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