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基于Luminex的2,4,6-三硝基甲苯(TNT)竞争性免疫分析方法的开发。

Development of a Luminex based competitive immunoassay for 2,4,6-trinitrotoluene (TNT).

作者信息

Anderson George P, Lamar Jacqueline D, Charles Paul T

机构信息

Center for Bio/Molecular Science and Engineering, U.S. Naval Research Laboratory, Washington, DC, USA.

出版信息

Environ Sci Technol. 2007 Apr 15;41(8):2888-93. doi: 10.1021/es062333n.

Abstract

Previously, a displacement immunoassay for 2,4,6-trinitrotoluene (TNT) was demonstrated using the Luminex 100. The work presented utilized this same specialized flow cytometer to demonstrate a highly sensitive and rapid competitive immunoassay for TNT. This required a TNT analog to be attached to the microsphere surface. Various linkers were evaluated; bovine serum albumin provided over 3 times more binding sites in comparison to various shorter diamine linkers. For this assay TNB-coated microspheres were added to samples; then biotinylated anti-TNT antibody and the reporter molecule, Streptavidin-R-Phycoerythrin, were added. In the absence of TNT, a highly fluorescent complex was formed on the surface of the microsphere. The presence of TNT resulted in dose-dependent decreased fluorescence. Various anti-TNT antibodies were evaluated; Mab 30-1 gave the strongest response, yielding the lowest limit of detection (<1.0 ng/mL) and a dynamic range up to 1 microg/mL. Other factors such as reaction time, cross reactivity to other nitro-compounds, evaluation of acetone extracts of TNT contaminated soils, testing in environmental matrices such as fresh water and seawater were all completed. Finally, a multiplex assay for TNT and three protein toxins was successfully conducted using the competitive format.

摘要

此前,利用Luminex 100展示了一种用于2,4,6-三硝基甲苯(TNT)的置换免疫测定法。本文介绍的工作利用了同一台专业流式细胞仪来展示一种针对TNT的高灵敏度快速竞争免疫测定法。这需要将一种TNT类似物连接到微球表面。对各种连接子进行了评估;与各种较短的二胺连接子相比,牛血清白蛋白提供的结合位点多出3倍以上。对于该测定法,将包被有TNB的微球加入样品中;然后加入生物素化抗TNT抗体和报告分子链霉亲和素-R-藻红蛋白。在不存在TNT时,在微球表面形成高度荧光复合物。TNT的存在导致荧光呈剂量依赖性降低。对各种抗TNT抗体进行了评估;单克隆抗体30-1给出了最强响应,检测限最低(<1.0 ng/mL),动态范围高达1 μg/mL。还完成了其他因素的研究,如反应时间、对其他硝基化合物的交叉反应性、对TNT污染土壤丙酮提取物的评估、在淡水和海水等环境基质中的测试。最后,使用竞争模式成功进行了TNT和三种蛋白质毒素的多重测定。

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