Life Sciences Division, National Research Council of Canada, 75 de Mortagne Boulevard, Boucherville, Quebec J4B 6Y4, Canada.
Health Canada, Bureau of Microbial Hazards, 251 Sir Frederick Banting Driveway, Ottawa, Ontario K1A 0K9, Canada.
Anal Chem. 2020 Jun 2;92(11):7738-7745. doi: 10.1021/acs.analchem.0c00830. Epub 2020 Apr 29.
We describe the use of periodic micropillar arrays, produced from cyclic olefin copolymer using high-fidelity microfabrication, as templates for colorimetric DNA detection. The assay involves PCR-amplified gene markers for O157:H7 (, , , and ) incorporating a detectable digoxigenin label, which is revealed through an immunoenzymatic process following hybridization with target-specific oligonucleotide capture probes. The capacity of micropillar arrays to induce wicking is used to distribute and confine capture probes with spatial control, making it possible to achieve a uniform signal while allowing multiple, independent probes to be arranged in close proximity on the same substrate. The kinetic profile of color pigment formation on the surface was followed using absorbance measurements, showing maximum signal increase between 20 and 60 min of reaction time. The relationship between microstructure and colorimetric signal was investigated through variation of geometric parameters, such as pitch (10-50 μm), pillar diameter (5-40 μm), and height (16-48 μm). Our findings suggest that signal intensity is largely influenced by the edges of the pillars and less by their height such that it deviates from a linear relationship when both aspect ratio and pillar density become very high. A theoretical model used to simulate the changes in surface composition at the molecular level suggests that differences in the temporal and spatial accumulation of assay components account for this observation.
我们描述了使用周期性微柱阵列作为比色 DNA 检测的模板,该微柱阵列由环烯烃共聚物通过高保真微加工制成。该测定法涉及 PCR 扩增的 O157:H7 基因标记物(stx1、stx2、eae 和 fliC),其中包含可检测的地高辛标记物,通过与目标特异性寡核苷酸捕获探针杂交后的免疫酶过程揭示出来。微柱阵列诱导芯吸的能力用于以空间控制的方式分配和限制捕获探针,从而可以实现均匀的信号,同时允许在同一基底上近距离排列多个独立的探针。通过吸光度测量跟踪表面上色素形成的动力学曲线,显示在 20-60 分钟的反应时间之间信号最大增加。通过改变几何参数(例如节距(10-50μm)、柱直径(5-40μm)和高度(16-48μm))来研究微观结构和比色信号之间的关系。我们的研究结果表明,信号强度主要受柱子边缘的影响,而高度的影响较小,因此当纵横比和柱子密度变得非常高时,它会偏离线性关系。用于模拟分子水平表面组成变化的理论模型表明,测定成分的时间和空间积累的差异解释了这一观察结果。