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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Rapid and simultaneous detection of ricin, staphylococcal enterotoxin B and saxitoxin by chemiluminescence-based microarray immunoassay
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Rapid and simultaneous detection of ricin, staphylococcal enterotoxin B and saxitoxin by chemiluminescence-based microarray immunoassay

机译:基于化学发光的微阵列免疫分析法可同时快速检测蓖麻毒蛋白,葡萄球菌肠毒素B和毒素

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摘要

Simultaneous detection of small and large molecules on microarray immunoassays is a challenge that limits some applications in multiplex analysis. This is the case for biosecurity, where fast, cheap and reliable simultaneous detection of proteotoxins and small toxins is needed. Two highly relevant proteotoxins, ricin (60 kDa) and bacterial toxin staphylococcal enterotoxin B (SEB, 30 kDa) and the small phycotoxin saxitoxin (STX, 0.3 kDa) are potential biological warfare agents and require an analytical tool for simultaneous detection. Proteotoxins are successfully detected by sandwich immunoassays, whereas competitive immunoassays are more suitable for small toxins (<1 kDa). Based on this need, this work provides a novel and efficient solution based on anti-idiotypic antibodies for small molecules to combine both assay principles on one microarray. The biotoxin measurements are performed on a flow-through chemiluminescence microarray platform MCR3 in 18 minutes. The chemiluminescence signal was amplified by using a poly-horseradish peroxidase complex (polyHRP), resulting in low detection limits: 2.9 ± 3.1 μg L~(-1) for ricin, 0.1 ± 0.1 μg L~(-1) for SEB and 2.3 ± 1.7 μg L~(-1) for STX. The developed multiplex system for the three biotoxins is completely novel, relevant in the context of biosecurity and establishes the basis for research on anti-idiotypic antibodies for microarray immunoassays.
机译:在微阵列免疫分析中同时检测大小分子是一项挑战,限制了多重分析中的某些应用。这是生物安全的情况,其中需要快速,廉价和可靠地同时检测蛋白毒素和小毒素。两种高度相关的蛋白毒素,蓖麻毒素(60 kDa)和细菌毒素葡萄球菌肠毒素B(SEB,30 kDa)和小的植物毒素毒毒素(STX,0.3 kDa)是潜在的生物战剂,需要同时检测的分析工具。蛋白蛋白毒素可通过夹心免疫测定法成功检测,而竞争性免疫测定法更适用于小毒素(<1 kDa)。基于这一需要,这项工作为小分子提供了一种基于抗独特型抗体的新颖有效的解决方案,以将两种测定原理结合在一个微阵列上。在18分钟内在流通式化学发光微阵列平台MCR3上进行生物毒素测量。化学发光信号通过使用辣根过氧化物酶复合物(polyHRP)进行扩增,检测限较低:蓖麻毒蛋白为2.9±3.1μgL〜(-1),SEB为0.1±0.1μgL〜(-1),2.3 STX为±1.7μgL〜(-1)所开发的三种生物毒素的多重系统是全新的,在生物安全性方面具有重要意义,并为微阵列免疫分析抗独特型抗体的研究奠定了基础。

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