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用于蓝藻肽类肝毒素(微囊藻毒素和节球藻毒素)的广谱非竞争性免疫复合物免疫测定法

Broad-Spectrum Noncompetitive Immunocomplex Immunoassay for Cyanobacterial Peptide Hepatotoxins (Microcystins and Nodularins).

作者信息

Akter Sultana, Vehniäinen Markus, Spoof Lisa, Nybom Sonja, Meriluoto Jussi, Lamminmäki Urpo

机构信息

Molecular Biotechnology and Diagnostics, Department of Biochemistry, University of Turku , FI-20520 Turku, Finland.

Biochemistry, Faculty of Science and Engineering, Åbo Akademi University , FI-20520 Turku, Finland.

出版信息

Anal Chem. 2016 Oct 18;88(20):10080-10087. doi: 10.1021/acs.analchem.6b02470. Epub 2016 Oct 4.

Abstract

A broad-spectrum noncompetitive immunoassay allowing sensitive and simple detection of a group of similar compounds would be an ideal tool for screening low-molecular weight analytes (<2000 Da) having many variants. However, the development of an essential antibody pair capable of sandwich-type recognition of the analytes' small generic core structure is a demanding task due to limited space available for simultaneous binding of two different antibodies. We report here a generic noncompetitive assay for cyanobacterial microcystins (MCs) and nodularins (Nod), a group of structurally related small cyclic peptides (∼1000 Da) with more than 100 naturally occurring analogs. The assay is based on the unique combination of a generic anti-immunocomplex (anti-IC) single-chain fragment of antibody variable domain (scFv) and a monoclonal antibody capable of binding to an Adda-group (3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4(E),6(E)-dienoic acid) present in all MCs/Nod. The anti-IC scFv was isolated from a large synthetic antibody library with phage display and used to develop a single-step sandwich-type noncompetitive immunocomplex assay. The sensitive time-resolved immunofluorometry-based assay is capable of detecting all the 11 tested commonly occurring hepatotoxins (MC-LR, -dmlR, -RR, -dmRR, -LA, -LY, -LF, -LW, -YR, -WR, and Nod-R) at concentration below 0.1 μg/L in a 1 h assay. Using MC-LR, the most studied toxic and widely distributed of the toxins, the calculated detection limits (based on blank + 3SD response) are ∼0.026 μg/L in 1 h and ∼0.1 μg/L in 10 min assay time. This is by far the fastest reported immunoassay for MCs and Nod with a detection limit far below the World Health Organization's guideline limit (1 μg/L of MC-LR equivalent in drinking water). The assay was validated with spiked tap and lake water as well as with environmental surface water samples. The developed assay provides a simple, rapid, and highly sensitive tool for the quantitative detection of MCs/Nod with the additional benefit of automation and high-throughput possibilities for large scale screening of drinking and environmental surface water samples. Furthermore, the study describes the first demonstration of the assay intended for the detection of an analyte group comprising similar low-molecular weight compounds exhibiting the benefits of a reagent excess type assay.

摘要

一种能够灵敏且简便地检测一组相似化合物的广谱非竞争性免疫测定法,将是筛选具有多种变体的低分子量分析物(<2000 Da)的理想工具。然而,由于可供两种不同抗体同时结合的空间有限,开发一种能够以夹心型方式识别分析物小通用核心结构的关键抗体对是一项艰巨的任务。我们在此报告一种针对蓝藻微囊藻毒素(MCs)和节球藻毒素(Nod)的通用非竞争性测定法,这是一组结构相关的小环肽(~1000 Da),有100多种天然存在的类似物。该测定法基于抗体可变域的通用抗免疫复合物(anti-IC)单链片段(scFv)与一种能够结合所有MCs/Nod中都存在的Adda基团(3-氨基-9-甲氧基-2,6,8-三甲基-10-苯基癸-4(E),6(E)-二烯酸)的单克隆抗体的独特组合。通过噬菌体展示从一个大型合成抗体库中分离出anti-IC scFv,并用于开发一种单步夹心型非竞争性免疫复合物测定法。基于灵敏的时间分辨免疫荧光法的测定法能够在1小时的测定中检测浓度低于0.1 μg/L的所有11种测试的常见肝毒素(MC-LR、-dmlR、-RR、-dmRR、-LA、-LY、-LF、-LW、-YR、-WR和Nod-R)。以研究最多且分布广泛的毒素MC-LR为例,计算得出的检测限(基于空白+3SD响应)在1小时测定中约为0.026 μg/L,在10分钟测定时间中约为0.1 μg/L。这是迄今为止报道的针对MCs和Nod最快的免疫测定法,其检测限远低于世界卫生组织的指导限值(饮用水中相当于1 μg/L的MC-LR)。该测定法通过加标的自来水和湖水以及环境地表水样品进行了验证。所开发的测定法为MCs/Nod的定量检测提供了一种简单、快速且高度灵敏的工具,还具有自动化以及对饮用水和环境地表水样品进行大规模筛选的高通量可能性的额外优势。此外,该研究首次展示了一种用于检测包含相似低分子量化合物的分析物组的测定法,该测定法具有试剂过量型测定法的优点。

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