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Inhibitory effect of the adenovirus type 5 E1A protein expressed in the yeast system on the human tumor cell growth

机译:在酵母系统中表达的5型腺病毒E1A腺病毒对人肿瘤细胞生长的抑制作用

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摘要

Adenovirus 5 type E1A as a tumor suppressor gene can inhibit tumor growth and enhance the sensitivity of chemotherapy and radiotherapy. E1A have the ability to integrate into the host genome, resulting in long-time expression that induces Rb gene inactivation and animal cells immortalization. This prompted us to select the E1A protein for treatment of cancer in order to overcome the limitations of E1A gene therapy. Thus, we firstly constructed E1A eucaryotic expression vector (pPIC9/E1A), transformated the pichia pastoris yeast cells (GS115) and screened the high-expressing recombinant strains. The positive yeast strains were cultured in the shake flask, and induced for 3 d. The crude E1A protein was purified using two steps of column chromatography on HiTrap Q and HiTrap SP. The purified E1A protein was identified by SDS-PAGE and Western blot. E1A protein was mostly located at cellular nuclear when Chariot delivered E1A protein arrested LN686 cell cycle LN686 tumor cells. The current studies firstly provided an experimental basis to further develop E1A protein for tumor treatment.
机译:腺病毒5型E1A作为抑癌基因可以抑制肿瘤生长,增强化疗和放疗的敏感性。 E1A具有整合入宿主基因组的能力,从而导致长时间表达,从而诱导Rb基因失活和动物细胞永生化。这促使我们选择E1A蛋白来治疗癌症,以克服E1A基因治疗的局限性。因此,我们首先构建了E1A真核表达载体(pPIC9 / E1A),转化了毕赤酵母酵母细胞(GS115),并筛选了高表达重组菌株。将阳性酵母菌株在摇瓶中培养,并诱导3 d。使用HiTrap Q和HiTrap SP的两步柱色谱法纯化E1A粗蛋白。通过SDS-PAGE和Western blot鉴定纯化的E1A蛋白。当Chariot递送E1A蛋白使LN686细胞周期LN686肿瘤细胞停滞时,E1A蛋白主要位于细胞核。目前的研究首先为进一步开发用于肿瘤治疗的E1A蛋白提供了实验基础。

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