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METHOD FOR SYNTHESIS OF PHARMACEUTICAL RECOMBINANT PROTEIN BASED ON INTEIN

机译:基于内含肽的药物重组蛋白的合成方法

摘要

Disclosed is a method for the synthesis of a pharmaceutical recombinant protein based on an intein, comprising the following steps: construction of vector DNA fragments expressing a polypeptide having a targeting function and a polypeptide having a toxic function in an immunotoxin, the vector DNA fragments of the two polypeptides respectively being linked to the N-terminus or C-terminus of the intein to form a fusion expression vector; taking the fusion expression vector described in step 1, and expressing same to obtain a fusion polypeptide A that fuses the N-terminus of the intein and a fusion polypeptide B that fuses the C-terminus of the intein; taking the fusion polypeptide A and the fusion polypeptide B, mixing them, and inducing the mixture under trans-splicing conditions corresponding to the intein to obtain the immunotoxin. The method only requires the preparation of different targeting part polypeptides and toxic part polypeptides, wherein same can be combined and then produce an immunotoxin that can target different targets and have different toxic mechanisms, with significant diversity and flexibility.
机译:公开了一种基于内含肽的药物重组蛋白的合成方法,其包括以下步骤:构建表达在免疫毒素中具有靶向功能的多肽和具有毒性功能的多肽的载体DNA片段,所述两条多肽分别连接至所述内含肽的N端或C端以形成融合表达载体;取步骤1所述的融合表达载体,进行表达,得到融合内含子N末端的融合多肽A和融合内含子C末端的融合多肽B。取融合多肽A和融合多肽B,将其混合,并在与内含肽相对应的反式剪接条件下诱导混合物以获得免疫毒素。该方法仅需要制备不同的靶向部分多肽和毒性部分多肽,其中可以将它们结合,然后产生可以靶向不同靶标并具有不同毒性机制的免疫毒素,具有明显的多样性和灵活性。

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