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首页> 外文期刊>Journal of Virological Methods >Production of polyclonal antibodies against Pelargonium zonate spot virus coat protein expressed in Escherichia coli and application for immunodiagnosis
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Production of polyclonal antibodies against Pelargonium zonate spot virus coat protein expressed in Escherichia coli and application for immunodiagnosis

机译:抗在大肠杆菌中表达的天竺葵区带斑点病毒外壳蛋白的多克隆抗体的生产及免疫诊断应用

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摘要

Pelargonium zonate spot virus (PZSV) is identified recently in tomato plants in the United States. To develop serological diagnostic tools for the detection of this virus, the production of good quality antibodies is a necessity. The coat protein (CP) gene of a California isolate of PZSV was cloned into a bacterial expression vector (pTriEX-4 Ek/LIC). The plasmid pTriEX-4-PZSV-CP was transformed into Escherichia coli Rosetta 2(DE3)pLacI and the recombinant PZSV-CP was expressed as a fusion protein containing N-terminal hexa-histidine and S tags. Expressed PZSV-CP was purified under denaturing conditions by affinity chromatography yielding 3mg refolded protein per 200mL of bacterial culture, and used as an antigen for raising PZSV-CP antiserum in rabbits. Specificity of the antiserum to PZSV was shown by Western blot and ELISA. When used in Western blot analysis, the antiserum was able to detect the recombinant protein, the PZSV coat protein and PZSV infected plant samples. The antiserum was successfully used in indirect-ELISA at dilutions of up to 1:16,000 to detect PZSV in infected leaf samples. Direct ELISA was successful only with denatured antigens. This is the first report on production of polyclonal antiserum against recombinant coat protein of PZSV and its use for detection and diagnosis of virus using serological methods.
机译:最近在美国的番茄植物中鉴定出天竺葵带状斑病毒(PZSV)。为了开发用于检测该病毒的血清学诊断工具,必须生产高质量的抗体。将加利福尼亚州PZSV分离株的外壳蛋白(CP)基因克隆到细菌表达载体(pTriEX-4 Ek / LIC)中。将质粒pTriEX-4-PZSV-CP转化到大肠杆菌Rosetta 2(DE3)pLacI中,并将重组PZSV-CP表达为含有N末端六组氨酸和S标签的融合蛋白。表达的PZSV-CP在变性条件下通过亲和层析纯化,每200mL细菌培养物产生3mg折叠蛋白,并用作在兔中产生PZSV-CP抗血清的抗原。通过Western印迹和ELISA显示抗血清对PZSV的特异性。当用于蛋白质印迹分析时,抗血清能够检测重组蛋白,PZSV外壳蛋白和PZSV感染的植物样品。该抗血清已成功用于稀释度高达1:16,000的间接ELISA中,以检测感染叶样品中的PZSV。直接ELISA仅在变性抗原时才成功。这是有关针对PZSV重组外壳蛋白的多克隆抗血清生产及其通过血清学方法检测和诊断病毒的首次报道。

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