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Evaluation of a novel ultra-sensitive nanoparticle probe-based assay for ricin detection

机译:新型基于超灵敏纳米探针的蓖麻毒素检测方法的评估

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摘要

A gold nanoparticle (GNP) probe-based assay (GNPA) modified from the bio-barcode assay (BCA) was developed for ultrasensitive detection of ricin, a potential biothreat agent. In the GNPA, a chain of ricin was captured by a GNP probe coated with polyclonal antibodies and single-stranded signal DNA. A magnetic microparticle (MMP) probe coated with ricin A chain monoclonal antibody was then added to form an immuno-complex. After being magnetically separated, the immuno-complex containing the single-stranded signal DNA was characterized by PCR and real-time PCR. A detection limit of 10(-2) fg/ml was determined for the ricin A chain; this is eight orders of magnitude more sensitive than that achieved with an ELISA and two orders more sensitive than that obtained with the BCA. The coefficients of variation (CV) of the intra-and inter-assay values ranged from 3.82-6.46%. The results here show that this novel assay is an ultrasensitive method for detection of ricin proteins and may be suitable for the ultrasensitive detection of other proteins.
机译:从生物条形码测定法(BCA)改进的基于金纳米粒子(GNP)探针的测定法(GNPA)被开发用于超灵敏检测蓖麻毒蛋白,这是一种潜在的生物威胁剂。在GNPA中,被覆有多克隆抗体和单链信号DNA的GNP探针捕获了蓖麻毒蛋白链。然后加入涂有蓖麻蛋白A链单克隆抗体的磁性微粒(MMP)探针以形成免疫复合物。磁分离后,通过PCR和实时PCR对包含单链信号DNA的免疫复合物进行表征。蓖麻毒蛋白A链的检出限为10(-2)fg / ml。这比ELISA灵敏度高8个数量级,比BCA灵敏度高2个数量级。批内和批间值的变异系数(CV)为3.82-6.46%。此处的结果表明,这种新颖的测定方法是检测蓖麻毒素蛋白的超灵敏方法,可能适用于其他蛋白的超灵敏检测。

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