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GPC3-N蛋白及其纳米抗体的制备与表征

Production and characterization of GPC3-N protein and its nanobody.

作者信息

Lao Zhiting, Li Shuanqi, Liang Jinhui, Su Jingyi, Gong Xin, Cui Xiping, Zhao Suqing

机构信息

Department of Pharmaceutical Engineering, School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, 510006, People's Republic of China.

出版信息

Protein Expr Purif. 2022 Aug;195-196:106094. doi: 10.1016/j.pep.2022.106094. Epub 2022 Apr 15.

Abstract

Glypican-3 (GPC3) has a promise to be the diagnostic biomarker as well as therapeutic target for hepatocellular carcinoma (HCC). Nanobody have the great potential in clinical diagnosis and treatment for their characteristics of small size, high solubility, stability, manipulability, binding advantages, and ease of production. In this study, the recombinant glypican-3-N terminal (GPC3-N) protein was expressed as inclusion body in E. coli BL21(DE3)pLysS cells and then purified, which is then used as the immunogen to construct nanobody phage library. The positive clone (named MF15) was obtained by four rounds of bio-panning, and then transformed into the E. coil TOP10F' cells to express nanobody protein, with the molecular weight of 19 kDa. Both Western blot and immunofluorescence analysis revealed that bacterially expressed GPC3-N protein is biologically active, and MF15 could specifically recognized native GPC3 expressed in HepG2 cells. The results in this study would provide the technical support for the development of diagnostic kits and antibody drugs targeting GPC3.

摘要

磷脂酰肌醇蛋白聚糖-3(GPC3)有望成为肝细胞癌(HCC)的诊断生物标志物和治疗靶点。纳米抗体因其体积小、溶解度高、稳定性好、可操作性强、结合优势明显及易于生产等特点,在临床诊断和治疗中具有巨大潜力。在本研究中,重组磷脂酰肌醇蛋白聚糖-3-N端(GPC3-N)蛋白在大肠杆菌BL21(DE3)pLysS细胞中以包涵体形式表达,随后进行纯化,将其用作免疫原构建纳米抗体噬菌体文库。通过四轮生物淘选获得阳性克隆(命名为MF15),然后将其转化到大肠杆菌TOP10F'细胞中表达纳米抗体蛋白,分子量为19 kDa。蛋白质免疫印迹和免疫荧光分析均表明,细菌表达的GPC3-N蛋白具有生物活性,且MF15能够特异性识别HepG2细胞中表达的天然GPC3。本研究结果将为开发针对GPC3的诊断试剂盒和抗体药物提供技术支持。

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