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Rapid Prototyping of Microfluidic Systems in Poly(dimethylsiloxane).聚二甲基硅氧烷微流控系统的快速成型
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Attomolar detection of botulinum toxin type A in complex biological matrices.复杂生物基质中阿托摩尔水平A型肉毒杆菌毒素的检测
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Development of improved SNAP25 endopeptidase immuno-assays for botulinum type A and E toxins.用于A型和E型肉毒杆菌毒素的改良SNAP25内肽酶免疫测定法的开发。
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A capillary electrophoresis method to assay catalytic activity of botulinum neurotoxin serotypes: implications for substrate specificity.一种用于检测肉毒杆菌神经毒素血清型催化活性的毛细管电泳方法:对底物特异性的影响
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自组装肽单层作为阵列微通道内的毒素传感机制。

Self-assembled peptide monolayers as a toxin sensing mechanism within arrayed microchannels.

作者信息

Frisk Megan L, Tepp William H, Johnson Eric A, Beebe David J

机构信息

Department of Chemistry, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Anal Chem. 2009 Apr 1;81(7):2760-7. doi: 10.1021/ac802707u.

DOI:10.1021/ac802707u
PMID:19253949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2760437/
Abstract

A sensor for the lethal bacterial enzyme, botulinum neurotoxin type A (BoNT/A), was developed using self-assembled monolayers (SAMs). SAMs consisting of an immobilized synthetic peptide that mimicked the toxin's in vivo SNAP-25 protein substrate were formed on Au and interfaced with arrayed microfluidic channels. Efforts to optimize SAM composition and assay conditions for greatest reaction efficiency and sensitivity are described in detail. Channel design provided facile fluid manipulation, sample incubation, analyte concentration, and fluorescence detection all within a single microfluidic channel, thus avoiding sample transfer and loss. Peptide SAMs were exposed to varying concentrations of BoNT/A or its catalytic light chain (ALC), resulting in enzymatic cleavage of the peptide substrate from the surface. Fluorescence detection was achieved down to 20 pg/mL ALC and 3 pg/mL BoNT/A in 3 h. Toxin sensing was also accomplished in vegetable soup, demonstrating practicality of the method. The modular design of this microfluidic SAM platform allows for extension to sensing other toxins that operate via enzymatic cleavage, such as the remaining BoNT serotypes B-G, anthrax, and tetanus toxin.

摘要

利用自组装单分子层(SAMs)开发了一种用于检测致命细菌酶——A型肉毒杆菌神经毒素(BoNT/A)的传感器。由模拟毒素体内SNAP-25蛋白底物的固定化合成肽组成的SAMs在金表面形成,并与阵列式微流控通道相连。详细描述了为实现最大反应效率和灵敏度而优化SAM组成和检测条件的努力。通道设计实现了在单个微流控通道内进行便捷的流体操控、样品孵育、分析物浓缩和荧光检测,从而避免了样品转移和损失。肽SAMs暴露于不同浓度的BoNT/A或其催化轻链(ALC)中,导致肽底物从表面发生酶促裂解。在3小时内,荧光检测的下限达到20 pg/mL的ALC和3 pg/mL的BoNT/A。该方法还在蔬菜汤中实现了毒素传感,证明了其实用性。这种微流控SAM平台的模块化设计允许扩展到检测其他通过酶促裂解起作用的毒素,如其余的B - G型BoNT血清型、炭疽毒素和破伤风毒素。