绿色荧光标记C-反应蛋白的原核表达和毛细管电泳检测

2012-08-26 22:50

                作者:陈腾祥,夏高晓,陈丽,刘亚伟,刘靖华,姜勇 

【摘要】    目的: 表达纯化重组的His-EGFP-CRP蛋白,通过毛细管电泳技术对该重组蛋白的生物活性进行评价。方法: 用pET14b/EGFP-hCRP原核表达质粒转化到大肠杆菌BL21(DE3)中诱导表达,表达的重组蛋白通过亲和色谱纯化、梯度透析,获得复性的His-EGFP-CRP蛋白;并用高效毛细管电泳(HPCE)技术对复性的蛋白进行检测,了解蛋白质的等电点及活性。结果: 转化实验发现,该质粒pET14b/EGFP-hCRP在BL21(DE3)中能够被诱导表达;通过包涵体变性溶解、亲和色谱纯化可获得纯度较高的His-EGFP-CRP蛋白;HPCE分离发现复性后的His-EGFP-CRP蛋白峰为多个,其在电泳液pH值低于6时易检出,His-EGFP-CRP与THP-1细胞裂解物孵育后的检测峰增多。结论: 成功地在大肠杆菌BL21(DE3)中诱导表达重组蛋白His-EGFP-CRP,通过包涵体变性溶解及亲和色谱纯化获得该重组蛋白,复性后的His-EGFP-CRP等电点接近于6,以单体或多聚体等结构形式存在,具有结合活性,能与细胞内相关分子结合成复合物,可应用于CRP功能和内化机制的研究。

【关键词】  C反应蛋白; 基因表达; 蛋白质复性; 电泳,毛细管

  [Abstract] Objective: To express the purified recombinant protein, His-EGFP-CRP, and to evaluate the feasibility of its application in the research of function and internalization mechanism of human C-reactive protein (CRP). Methods: The re-constructed vector pET14b/EGFP-hCRP was transformed into Escherichia.coli BL21(DE3), induced by isopropyl-β-D-thiogalactopyranoside (IPTG). The expressed protein, His-EGFP-CRP, was purified with affinity chromatography method and refolded with gradient filtration. The renatured His-EGFP-CRP was analyzed with high performance capillary electrophoresis (HPCE) to evaluate its isoelectric point (pI) and bio-activity. Results: Fusion protein His-EGFP-CRP successfully expressed in transformed E. coli cells after the induction, and then was purified with inclusion lysis and affinity chromatography. His-EGFP-CRP was detected at several peaks of the fraction profile of HPCE when the pH of electrophoresis buffer was under 6. The number of His-EGFP-CRP detection peaks increased after the protein was incubated with lysate of THP-1 cells. Conclusions: The pI of His-EGFP-CRP is about 6, and its structures may be monomer or polymer, which have the ability to bind relative molecles in lysate of THP-1 to form complex. These results suggest the recombinant protein could be used in exploiting the function and internalization mechanism of human CRP.

  [Key words] C-reactive protein; gene expression; protein renaturation; electrophoresis,capillary

    C-反应蛋白(C-reactive protein, CRP)是一种发现较早的蛋白质,在急性心肌梗塞、创伤、感染、炎症、外科手术和肿瘤侵润时,其血浆浓度急剧升高,达到正常水平的数百倍,乃至数千倍,可以作为上述疾病的临床监测指标,是急性期蛋白的主要成员之一[1]。CRP在免疫反应过程中能识别病原体和宿主受损细胞,介导补体系统和吞噬细胞将它们清除,发挥免疫调理功能[2]。除此之外,近些年来研究表明CRP的功能十分复杂,发现其能通过胞膜进入培养的主动脉内皮细胞,从而参与粥样动脉硬化症等心血管疾病的发生[3~5]。然而,对于CRP内化进入细胞的行为和机制还缺乏深入的研究,原因之一是纯化原核表达的CRP有较大难度,不易获得有体外活性的重组表达物。为解决这一技术难题,构建了带his纯化标签和EGFP荧光标记的人CRP原核表达质粒[4]。在此工作基础上,对该融合蛋白的表达纯化和复性进行了探索,并利用高效毛细管电泳(high performance capillary electrophoresis, HPCE)技术对复性后的重组蛋白进行检测分析,以进一步了解该重组蛋白的基本理化特点,检测该蛋白的活性。

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