Laboratory of Biosensors and Bioelectronics, Institute for Biomedical Engineering, University and ETH Zurich, Gloriastrasse 35, 8092 Zurich, Switzerland.
ACS Appl Mater Interfaces. 2011 Jan;3(1):50-7. doi: 10.1021/am100849f. Epub 2010 Dec 9.
We present a simple, inexpensive, and sensitive technique for producing multiple copies of a hydrogel-based protein microarray. An agarose block containing 25 biofunctionalized channels is sliced perpendicularly to produce many identical biochips. Each microarray consists of 500 μm spots, which contain protein-coated microparticles physically trapped in porous SeaPrep agarose. Proteins diffuse readily through SeaPrep agarose, while the larger microparticles are immobilized in the hydrogel matrix. Without major assay optimization, the limit of detection is 12 pM for a sandwich assay detecting human IgG. These highly flexible, multiplexed arrays can be produced rapidly without any special instrumentation and are compatible with standard fluorescence-based read-out.
我们提出了一种简单、廉价且灵敏的技术,用于制备基于水凝胶的蛋白质微阵列的多个拷贝。含有 25 个生物功能化通道的琼脂糖块垂直切片可产生许多相同的生物芯片。每个微阵列由 500μm 的斑点组成,其中包含物理捕获在多孔 SeaPrep 琼脂糖中的涂覆蛋白质的微颗粒。蛋白质可轻易地在 SeaPrep 琼脂糖中扩散,而较大的微颗粒则固定在水凝胶基质中。无需进行重大分析优化,夹心检测法检测人 IgG 的检测限低至 12 pM。这些高度灵活、可多重检测的微阵列可以快速制备,无需特殊仪器,并且与基于标准荧光的读取兼容。