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An assay for the detection of grapevine leafroll-associated virus 3 using a single-chain fragment variable antibody.

机译:一种使用单链片段可变抗体检测葡萄叶相关病毒3的检测方法。

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摘要

Grapevine leafroll-associated virus 3 (GLRaV-3) is a major pathogen of grapevine. A previously described single-chain fragment variable (scFv) antibody (scFvLR3), directed against the coat protein (CP) of GLRaV-3, was expressed in Escherichia coli and used to develop a diagnostic ELISA kit. The antibody was fused to the light chain constant domain of human immunoglobulin to create the bivalent reagent C(L)-LR3, which was purified from the periplasmic fraction, giving a yield of ~5 mg/l. The sensitivity of the reagent against recombinant GLRaV-3 CP was 0.1 ng. The sensitivity, specificity and durability of the reagent was similar to a commercial kit. The C(L)-LR3 showed a weak cross-reaction in immune electron microscopy assays to GLRaV-1 and -7, but not with the phylogenetically more distant GLRaV-2. A fully recombinant kit was developed with the inclusion of a recombinant GLRaV-3 CP expressed in bacteria, thus avoiding problems associated with virus propagation and purification. This system representsa rapid, simple, sensitive and standardized diagnostic protocol for GLRaV-3 detection.
机译:葡萄卷叶相关病毒3(GLRaV-3)是葡萄的主要病原体。针对GLRaV-3外壳蛋白(CP)的先前描述的单链片段可变(scFv)抗体(scFvLR3)在大肠杆菌中表达,并用于开发诊断ELISA试剂盒。将抗体融合到人免疫球蛋白的轻链恒定域上,以生成二价试剂C(L)-LR3,将其从周质组分中纯化出来,产量约为5 mg / l。该试剂对重组GLRaV-3 CP的敏感性为0.1 ng。该试剂的敏感性,特异性和耐用性与市售试剂盒相似。 C(L)-LR3在针对GLRaV-1和-7的免疫电子显微镜检测中显示出较弱的交叉反应,但在系统发育上较远的GLRaV-2中却没有。开发了一种完全重组的试剂盒,其中包含在细菌中表达的重组GLRaV-3 CP,从而避免了与病毒繁殖和纯化有关的问题。该系统代表了用于GLRaV-3检测的快速,简单,灵敏和标准化的诊断协议。

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