首页> 外文期刊>Analytical chemistry >Immunoenzymometric Assay for a Small Molecule, 11-Deoxycortisol, with Attomole-Range Sensitivity Employing an scFv-Enzyme Fusion Protein and Anti-Idiotype Antibodies
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Immunoenzymometric Assay for a Small Molecule, 11-Deoxycortisol, with Attomole-Range Sensitivity Employing an scFv-Enzyme Fusion Protein and Anti-Idiotype Antibodies

机译:使用scFv-酶融合蛋白和抗独特型抗体的小分子11-脱氧皮质醇的原子比色测定法

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To overcome the sensitivity limit in immunoassays for small molecules (haptens), we established a noncompetitive immunoenzymometric assay (IEMA) format that can detect attomole-range hapten molecules. We selected 11-deoxycortisol (11-DC; M_(r) 346.5), a corticosteroid serving a diagnostic index for pituitary-adrenal function, as a model target hapten. A fusion of a single-chain Fv fragment (scFv) specific for 11-DC and alkaline phosphatase (ALP) was generated for use as an enzyme-labeled antibody, instead of the conventional chemically linked enzyme-antibody conjugates. After binding reaction of 11-DC and fixed amounts of the fusion protein (scFv-ALP), the unbound fusion protein was removed by incubation with a mouse beta-type anti-idiotype antibody recognizing the scFv paratope. These complexes were captured by magnetic separation using anti-mouse IgG antibody-coated magnetic beads. Following magnetic sedimentation of the beads, immune complexes of scFv-ALP and 11-DC remained in the supernatant were further purified by capture on microtiter plates with immobilized alpha-type antiidiotype antibody. As measured fluorometrically, ALP activity from bound immune complexes on the plates increased with increasing 11-DC, which is characteristic of a noncompetitive relationship. This IEMA afforded an extremely low detection limit (20 amol/assay), a very wide measurable range, and practical specificity. The plasma 11-DC levels determined for healthy subjects were validated as reliable.
机译:为了克服小分子(半抗原)免疫测定法中的灵敏度极限,我们建立了一种非竞争性免疫酶分析法(IEMA)格式,可以检测到在原子范围内的半抗原分子。我们选择11-脱氧皮质醇(11-DC; M_(r)346.5)作为模型目标半抗原,该皮质类固醇具有垂体-肾上腺功能的诊断指标。产生了对11-DC特异的单链Fv片段(scFv)与碱性磷酸酶(ALP)的融合体,用作酶标记的抗体,代替了常规的化学连接的酶抗体结合物。 11-DC与固定量的融合蛋白(scFv-ALP)发生结合反应后,通过与识别scFv对位的小鼠β型抗独特型抗体一起孵育来去除未结合的融合蛋白。这些复合物是通过使用抗小鼠IgG抗体包被的磁珠进行磁分离而捕获的。磁珠沉淀后,保留在上清液中的scFv-ALP和11-DC免疫复合物通过用固定的α型抗独特型抗体在微量滴定板上捕获而进一步纯化。如用荧光法测量的,板上结合免疫复合物的ALP活性随11-DC的增加而增加,这是非竞争性关系的特征。该IEMA提供了极低的检出限(20 amol /分析),非常宽的可测量范围和实用特异性。确定为健康受试者确定的血浆11-DC水平是可靠的。

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