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首页> 外文期刊>Analytical chemistry >Development of a high-affinity anti-domoic acid sheep scFv and its use in detection of the toxin in shellfish
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Development of a high-affinity anti-domoic acid sheep scFv and its use in detection of the toxin in shellfish

机译:一种高亲和力抗软骨藻酸绵羊scFv的研制及其在贝类毒素检测中的应用

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The potential of immunoassays as high-throughput screening tools for the detection of harmful substances in foods will only be realized when convenient methods are available for production of the high affinity antibodies needed for sensitive assay development. Recombinant antibodies offer advantages over traditional monoclonal antibodies in terms of ease of production, much greater antibody repertoire for selection, and versatility. We describe here the development of recombinant antibodies against the common shellfish toxin, domoic acid (DA), utilizing the sheep immunoglobulin system as an effective method for generating high affinity anti-hapten recombinant antibody fragments. A single-chain antibody fragment (scFv) library was generated from a sheep immunized with DA-bovine serum albumin conjugate, and anti-DA scFvs were isolated by phage-display. Three selected scFvs gave 150s of 2.6 to 58 ng/mL (8.3 - 186 nM) in competitive enzyme-linked immunosorbent assay (ELISA). Assay optimization with one of these scFvs gave a very reproducible standard curve with a range of 0.3 to 5.6 ng/mL (1.0 to 17.9 nM), a mean limit of quantification (LOQ, defined as the 120) of 0.5 ng/mL (1.6 nM), and a mean 150 of 1.2 ng/mL (3.9 nM). When the assay was used for the analysis of crude methanolic extracts of scallop tissues, results obtained correlated well with standard HPLC assay results (R-2, 0.90, n = 40; R-2, 0.81, n = 34), although ELISA results were lower than HPLC results. Adjusting the cutoff point for DA concentration accordingly from the regulatory 20 mg/kg, the potential of the sheep scFv-based ELISA for use as a screening assay for DA in shellfish extracts was demonstrated.
机译:只有当有方便的方法来生产灵敏检测开发所需的高亲和力抗体时,免疫测定作为检测食品中有害物质的高通量筛选工具的潜力才能实现。与传统单克隆抗体相比,重组抗体在易于生产、更多的抗体选择库和多功能性方面具有优势。我们在这里描述了针对常见贝类毒素软骨藻酸 (DA) 的重组抗体的开发,利用绵羊免疫球蛋白系统作为生成高亲和力抗半抗原重组抗体片段的有效方法。从用DA-牛血清白蛋白偶联物免疫的绵羊中生成单链抗体片段(scFv)文库,并通过噬菌体展示分离抗DA scFv。在竞争性酶联免疫吸附测定 (ELISA) 中,三个选定的 scFvs 的 150 个 2.6 至 58 ng/mL (8.3 - 186 nM) 的 scFvs 值为 2.6 至 58 ng/mL (8.3 - 186 nM)。使用其中一种scFvs进行检测优化,可获得非常可重复的标准曲线,范围为0.3至5.6 ng/mL(1.0至17.9 nM),平均定量限(LOQ,定义为120)为0.5 ng/mL (1.6 nM),平均150为1.2 ng/mL (3.9 nM)。当该测定用于分析扇贝组织的粗甲醇提取物时,获得的结果与标准HPLC测定结果(R-2,0.90,n = 40;R-2, 0.81, n = 34),但ELISA结果低于HPLC结果。从规定的 20 mg/kg 相应地调整 DA 浓度的临界点,证明了基于绵羊 scFv 的 ELISA 用作贝类提取物中 DA 筛选测定的潜力。

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