Anti-tumor vaccines, coding genes, expression vectors, expression engineering bacteria and applications targeting vegf and mucin1
An expression vector and anti-tumor technology, applied in the field of anti-tumor vaccines, can solve problems such as the lack of VEGF protein research, achieve convenient affinity chromatography, and inhibit tumor angiogenesis
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Embodiment 1
[0034] The anti-tumor vaccine fusion protein mVEGF165b-muc1 targeting VEGF and mucin1 uses mutated VEGF165b as the carrier of the epitope peptide of the tumor-associated antigen mucin1, and a piece of epitope peptide of mucin1 is fused at its C-terminus. Linked by GGSAAY, its amino acid sequence is as follows:
[0035]
[0036] Among them, the normal part is the amino acid sequence of mVEGF165b, the underlined part is the amino acid sequence of the connecting peptide GGSAAY, and the italic part is the amino acid sequence of the epitope peptide of the tumor-associated antigen mucin1.
[0037] The nucleotide sequence encoding the above amino acid sequence is as follows:
[0038]
[0039]
[0040]Wherein, the normal part is the nucleotide sequence of mVEGF165b, the underlined part is the nucleotide sequence of the connecting peptide GGSAAY, and the italic part is the nucleotide sequence of the epitope peptide of the tumor-associated antigen mucin1.
Embodiment 2
[0042] The anti-tumor vaccine expression vector targeting VEGF and mucin1, its construction steps are:
[0043] 1) Using restriction endonucleases Not I and EcoR I to double-enzyme pPIC9K vector and mVEGF165b-muc1 gene sequence (as shown in SEQ ID NO. The protected base, synthesized by Suzhou Jinweizhi Biotechnology Co., Ltd.), the enzyme digestion reaction system and reaction conditions are as follows:
[0044] Enzyme digestion reaction system of pPIC9K vector (100μl): pPIC9K vector (75ng / μl) 26.7μl, endonuclease Not I (10U / μl) 2μl, endonuclease EcoR I (10U / μl) 2μl, 10×H Buffer ( Enzyme digestion buffer) 10 μl, 0.1% BSA (bovine serum albumin) 10 μl, sterilized distilled water 49.3 μl; enzyme digestion reaction conditions: react at 37° C. for 3 hours;
[0045] Enzyme digestion reaction system of mVEGF165b-muc1 gene sequence (100μl): mVEGF165b-muc1 gene fragment (149ng / μl) 13.4μl, endonuclease Not I (10U / μl) 2μl, endonuclease EcoR I (10U / μl) 2μl , 10×H Buffer (digestion buffe...
Embodiment 3
[0056] The anti-tumor vaccine expression engineering bacteria targeting VEGF and mucin1, the construction process is as follows: use the restriction endonuclease Sal I to digest the above pPIC9K-mVEGF165b-muc1 expression vector to obtain the linearized pPIC9K-mVEGF165b-muc1 expression vector, and then Transform Pichia pastoris GS115 competent cells, screen positive colonies, and cultivate high-copy positive clone colonies. The specific operations are as follows:
[0057] 1) Linearization of pPIC9K-mVEGF165b-muc1 expression vector
[0058] The pPIC9K-mVEGF165b-muc1 expression vector was digested with the restriction endonuclease Sal I, and the digested product was precipitated by adding 20 μl of 3mol / L NaAc solution (pH=5.2) and 400 μl of absolute ethanol, and at 4° C. Centrifuge at 12000rpm for 10 minutes, wash the precipitate with 70% (v / v) alcohol, then centrifuge at 12000rpm for 10 minutes, dissolve the precipitate in 20 μl of sterile deionized water after drying, and take ...
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