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用于微流控蛋白质电泳的光图案化独立聚丙烯酰胺凝胶。

Photopatterned free-standing polyacrylamide gels for microfluidic protein electrophoresis.

机构信息

University of California, Berkeley-University of California, San Francisco Graduate Program in Bioengineering, 342 Stanley Hall, Berkeley, California 94720, USA.

出版信息

Lab Chip. 2013 Jun 7;13(11):2115-23. doi: 10.1039/c3lc50269d.

Abstract

Designed for compatibility with slab-gel polyacrylamide gel electrophoresis (PAGE) reagents and instruments, we detail development of free-standing polyacrylamide gel (fsPAG) microstructures supporting electrophoretic performance rivalling that of microfluidic platforms. For the protein electrophoresis study described here, fsPAGE lanes are comprised of a sample reservoir and contiguous separation gel. No enclosed microfluidic channels are employed. The fsPAG devices (120 μm tall) are directly photopatterned atop of and covalently attached to planar polymer or glass surfaces. Leveraging the fast <1 h design-prototype-test cycle - significantly faster than mold based fabrication techniques - we optimize the fsPAG architecture to minimize injection dispersion for rapid (<1 min) and short (1 mm) protein separations. The facile fabrication and prototyping of the fsPAGE provides researchers a powerful tool for developing custom analytical assays. We highlight the utility of assay customization by fabricating a polyacrylamide gel with a spatial pore-size distribution and demonstrate the resulting enhancement in separation performance over a uniform gel. Further, we up-scale from a unit separation to an array of 96 concurrent fsPAGE assays in 10 min run time driven by one electrode pair. The fsPAG array layout matches that of a 96-well plate to facilitate integration of the planar free standing gel array with multi-channel pipettes while remaining compatible with conventional slab-gel PAGE reagents, such as staining for label-free protein detection. Notably, the entire fsPAGE workflow from fabrication, to operation, and readout uses readily available materials and instruments - making this technique highly accessible.

摘要

我们设计的自由站立聚丙烯酰胺凝胶(fsPAG)微结构与板凝胶聚丙烯酰胺凝胶电泳(PAGE)试剂和仪器兼容,可支持与微流控平台相媲美的电泳性能。在本文描述的蛋白质电泳研究中,fsPAGE 泳道由样品库和连续分离凝胶组成。不使用封闭的微流道。fsPAG 器件(高 120μm)直接在平面聚合物或玻璃表面上进行光图案化并通过共价键连接。利用快速的<1 小时设计-原型-测试周期 - 比基于模具的制造技术快得多 - 我们优化了 fsPAG 架构,以最小化注入分散,从而实现快速(<1 分钟)和短(<1mm)的蛋白质分离。fsPAGE 的易于制造和原型制作为研究人员提供了开发定制分析测定的强大工具。我们通过制造具有空间孔径分布的聚丙烯酰胺凝胶来突出测定定制的实用性,并展示了与均匀凝胶相比,分离性能的提高。此外,我们通过一对电极将分离从一个单元扩展到 96 个并行 fsPAGE 测定,在 10 分钟的运行时间内达到 96 个泳道,从而实现高通量。fsPAG 阵列布局与 96 孔板匹配,便于将平面自由站立凝胶阵列与多通道移液器集成,同时与传统的板凝胶 PAGE 试剂(例如用于无标记蛋白质检测的染色)兼容。值得注意的是,从制造到操作再到读数的整个 fsPAGE 工作流程都使用了现成的材料和仪器 - 使得该技术非常容易获得。

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