Barbee Kristopher D, Hsiao Alexander P, Heller Michael J, Huang Xiaohua
Department of Bioengineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412, USA.
Lab Chip. 2009 Nov 21;9(22):3268-74. doi: 10.1039/b912876j. Epub 2009 Sep 15.
We report a method for rapid, electric field directed assembly of high-density protein-conjugated microbead arrays. Photolithography is used to fabricate an array of micron to sub-micron-scale wells in an epoxy-based photoresist on a silicon wafer coated with a thin gold film, which serves as the primary electrode. A thin gasket is used to form a microfluidic chamber between the wafer and a glass coverslip coated with indium-tin oxide, which serves as the counter electrode. Streptavidin-conjugated microbeads suspended in a low conductance buffer are introduced into the chamber and directed into the wells via electrophoresis by applying a series of low voltage electrical pulses across the electrodes. Hundreds of millions of microbeads can be permanently assembled on these arrays in as little as 30 seconds and the process can be monitored in real time using epifluorescence microscopy. The binding of the microbeads to the gold film is robust and occurs through electrochemically induced gold-protein interactions, which allows excess beads to be washed away or recycled. The well and bead sizes are chosen such that only one bead can be captured in each well. Filling efficiencies greater than 99.9% have been demonstrated across wafer-scale arrays with densities as high as 69 million beads per cm(2). Potential applications for this technology include the assembly of DNA arrays for high-throughput genome sequencing and antibody arrays for proteomic studies. Following array assembly, this device may also be used to enhance the concentration-dependent processes of various assays through the accelerated transport of molecules using electric fields.
我们报道了一种用于高密度蛋白质缀合微珠阵列的快速、电场导向组装方法。光刻技术用于在涂有薄金膜的硅片上的环氧基光刻胶中制造微米到亚微米级的孔阵列,该金膜用作主电极。使用薄垫片在硅片和涂有氧化铟锡的玻璃盖玻片之间形成微流体腔室,氧化铟锡用作对电极。悬浮在低电导缓冲液中的链霉亲和素缀合微珠被引入腔室,并通过在电极上施加一系列低电压电脉冲,通过电泳引导到孔中。数亿个微珠可以在短短30秒内永久组装在这些阵列上,并且可以使用落射荧光显微镜实时监测该过程。微珠与金膜的结合牢固,通过电化学诱导的金-蛋白质相互作用发生,这使得多余的珠子可以被冲走或回收利用。选择孔和珠子的尺寸,使得每个孔中只能捕获一个珠子。在密度高达每平方厘米6900万个珠子的晶圆级阵列上,填充效率已证明大于99.9%。该技术的潜在应用包括用于高通量基因组测序的DNA阵列组装和用于蛋白质组学研究的抗体阵列组装。在阵列组装之后,该装置还可用于通过使用电场加速分子运输来增强各种测定的浓度依赖性过程。