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Isolation and detection of single molecules on paramagnetic beads using sequential fluid flows in microfabricated polymer array assemblies

机译:使用微细加工的聚合物阵列组件中的连续流体流分离和检测顺磁珠上的单个分子

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We report a method for isolating individual paramagnetic beads in arrays of femtolitre-sized wells and detecting single enzyme-labeled proteins on these beads using sequential fluid flows in microfabricated polymer array assemblies. Arrays of femtolitre-sized wells were fabricated in cyclic olefin polymer (COP) using injection moulding based on DVD manufacturing. These arrays were bonded to a complementary fluidic structure that was also moulded in COP to create an enclosed device to allow delivery of liquids to the arrays. Enzyme-associated, paramagnetic beads suspended in aqueous solutions of enzyme substrate were delivered fluidically to the array such that one bead per well was loaded by gravity. A fluorocarbon oil was then flowed into the device to remove excess beads from the surface of the array, and to seal and isolate the femtolitre-sized wells containing beads and enzyme substrate. The device was then imaged using standard fluorescence imaging to determine which wells contained single enzyme molecules. The analytical performance of this device as the detector for digital ELISA compared favourably to the standard method, i.e., glass arrays mechanically sealed against a silicone gasket; prostate specific antigen (PSA) could be detected from 0.011 pg mL~(-1) up to 100 pg mL~(-1). The use of an enclosed fluidic device to isolate beads in single-molecule arrays offers a multitude of advantages for low-cost manufacturing, ease of automation, and instrument development to enable applications in biomarker validation and medical diagnosis.
机译:我们报告了一种方法,用于分离飞秒大小的孔阵列中的单个顺磁珠,并使用微加工的聚合物阵列组件中的顺序流体流来检测这些珠上的单个酶标记蛋白。使用基于DVD制造的注塑成型技术,在环状烯烃聚合物(COP)中制造了飞米级孔阵列。这些阵列被结合到互补的流体结构上,该互补的流体结构也在COP中模制成型,以形成一个封闭的装置,以允许将液体输送到阵列中。将悬浮在酶底物水溶液中的与酶相关的顺磁性珠粒流体地递送至阵列,使得每孔一个珠粒通过重力加载。然后将碳氟化合物油流入设备中,以从阵列表面去除多余的珠子,并密封并分离出含有珠子和酶底物的飞轮大小的孔。然后使用标准荧光成像对设备成像,以确定哪些孔包含单个酶分子。该设备作为数字ELISA检测器的分析性能优于标准方法,即用硅胶垫圈机械密封的玻璃阵列;从0.011 pg mL〜(-1)到100 pg mL〜(-1)均可检测到前列腺特异性抗原(PSA)。使用封闭的流体装置分离单分子阵列中的珠子可为低成本制造,易于自动化和仪器开发提供众多优势,从而使其能够应用于生物标记物验证和医学诊断。

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