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一种使用单链抗体可变片段检测葡萄卷叶相关病毒3的分析方法。

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

作者信息

Cogotzi Laura, Giampetruzzi Annalisa, Nölke Greta, Orecchia Martin, Elicio Vito, Castellano Maria Antonietta, Martelli Giovanni P, Fischer Rainer, Schillberg Stefan, Saldarelli Pasquale

机构信息

Institute of Plant Virology, CNR, Bari, Italy.

出版信息

Arch Virol. 2009;154(1):19-26. doi: 10.1007/s00705-008-0263-y. Epub 2008 Dec 11.

Abstract

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 represents a rapid, simple, sensitive and standardized diagnostic protocol for GLRaV-3 detection.

摘要

葡萄卷叶相关病毒3(GLRaV-3)是葡萄的一种主要病原体。一种先前描述的针对GLRaV-3衣壳蛋白(CP)的单链可变片段(scFv)抗体(scFvLR3)在大肠杆菌中表达,并用于开发一种诊断ELISA试剂盒。该抗体与人免疫球蛋白轻链恒定区融合,产生二价试剂C(L)-LR3,其从周质部分纯化,产量约为5 mg/l。该试剂对重组GLRaV-3 CP的灵敏度为0.1 ng。该试剂的灵敏度、特异性和耐用性与商业试剂盒相似。C(L)-LR3在免疫电子显微镜检测中对GLRaV-1和-7显示出微弱的交叉反应,但与系统发育上更远的GLRaV-2没有交叉反应。通过包含在细菌中表达的重组GLRaV-3 CP,开发了一种完全重组的试剂盒,从而避免了与病毒繁殖和纯化相关的问题。该系统代表了一种用于GLRaV-3检测的快速、简单、灵敏和标准化的诊断方案。

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