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Abrin-a A-chain expressed as soluble form in Escherichia coli from a PCR-synthesized gene is catalytically and functionally active

机译:通过PCR合成的基因在大肠杆菌中以可溶形式表达的Abrin-A链具有催化和功能活性

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摘要

Abrin-a A chain (ABRaA) is a potent plant toxin, which possesses N-glycosylase activity toward eukaryotic 28S rRNA, and may have potential use in cancer therapy. To improve levels of expression in Escherichia coli, the gene encoding ABRaA was optimized by replacing rare codons with high-frequency ones, and synthesized using two-step PCR. The optimized ABRaA was cloned into the pET-His vector, and highly expressed in cytoplasm of E. coli. The yield of the purified recombinant (r) ABRaA proteins was up to 80 mg/l of induced culture. The rABRaA was one-step purified to homogeneity and its RNA-N-glycosylase ability to inhibit protein biosynthesis in a cell-free system and to depurinate 28S rRNA in rat liver ribosomes was demonstrated in vitro. The MTT assay showed that it also had a killing effect on human hepatoma cell line SMMC-7721 and myeloma cell line Sp2/0. For the first time, ABRaA expressed as soluble form in E. coli from a PCR-synthesized gene is catalytically and functionally active.
机译:Abrin-a A链(ABRaA)是有效的植物毒素,对真核28S rRNA具有N-糖基化酶活性,可能在癌症治疗中具有潜在用途。为了提高在大肠杆菌中的表达水平,通过用高频密码子替换稀有密码子来优化编码ABRaA的基因,并使用两步PCR进行合成。将优化的ABRaA克隆到pET-His载体中,并在大肠杆菌的细胞质中高度表达。纯化的重组(r)ABRaA蛋白的产量高达80 mg / l诱导培养。将rABRaA一步纯化至均质,并在体外证明了其RNA-N-糖基化酶抑制无细胞系统中蛋白质生物合成和使大鼠肝核糖体中28S rRNA脱嘌呤的能力。 MTT分析表明,它也对人肝癌细胞SMMC-7721和骨髓瘤Sp2 / 0具有杀伤作用。 PCR合成的基因在大肠杆菌中以可溶性形式表达的ABRaA首次具有催化和功能活性。

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