Recombinant target fusion protein GnRH-TNFam and its antitumor use
A fusion protein and targeting technology, which can be used in anti-tumor drugs, recombinant DNA technology, drug combinations, etc., and can solve problems such as large toxic side effects and poor specificity.
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Embodiment 1
[0042] Example 1. Acquisition of the gene GnRH-TNFαm encoding the recombinant targeting fusion protein
[0043] 1.PCR primers and their sequences
[0044] pvt3: 5'-TTA GAATTC CCGCCACCGGCCGTACCGGGTCCAAGATCA-3’
[0045] EcoRI
[0046] Pvt4: 5'-TAT GGATCC TTATCA CAGGGCAATGAT-3'
[0047] BamHI Stop codons
[0048] Pgt1: 5'-AAA CATATG CAGCACTGGTCCTATGGTCTGCGCCCTGGC GAATTC CCGCCACCG-3'
[0050] Pgt2: 5'-AAA CATATG CAGCACTGGTCCCATGGTTGGTGTCCGGGC GAATTC CCGCCACCG-3'
[0052] 2. Acquisition of mutant TNFα cDNA (TNFαm)
[0053] The recombinant plasmid pLT9KGITNFαm ( figure 1 ) was specifically amplified to obtain the cDNA of mutant TNFα (TNFαm). As a result, an EcoRI site ( GAA TTC ) and codons for several additional amino acids GAA TTC CCG CCA CCG GCC GTA CCG GGT CCA AGA TCA (underlined in bold). The amino acid sequence corresponding to this coding seque...
Embodiment 2
[0056] Example 2. Construction of fusion gene GnRH-TNFαm temperature-controlled expression recombinant pLTEGTI
[0057] In order to express the fusion gene GnRH-TNFαm into the fusion protein GnRH-TNFαm in E.coli, it was cloned into the NdeI / BamHI of the E.coli expression vector pCW111 constructed in our laboratory, so that its expression was placed in temperature promoter P R P L under control. The construction process is as follows: carry out NdeI / BamHI double enzyme digestion on pLTSKGTI, recover the fusion gene GnRH-TNFαm fragment, and then connect it with the expression vector pCW111 treated in the same way, so as to obtain the temperature-controlled expression recombinant pLTEGTI of the fusion gene GnRH-TNFαm ( Figure 5 ). The identification results of the enzyme digestion map were in line with expectations.
Embodiment 3
[0058] Example 3. Construction of the IPTG-inducible expression vector pLT30GTI of the fusion gene GnRH-TNFαm
[0059] The construction process of pLT30GTI is as follows: carry out NdeI / BamHI double enzyme digestion on pLTSKGTI, recover the fusion gene GnRH-TNFαm fragment, and then connect it with the expression vector pET30 treated in the same way, so as to obtain the IPTG-inducible expression recombinant of the fusion gene GnRH-TNFαm pLT30GTI ( Figure 6 ). The identification results of the enzyme digestion map were in line with expectations.
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