Department of Bioengineering University of Utah Salt Lake City, UT 84112, USA.
Small. 2010 Jul 5;6(13):1415-21. doi: 10.1002/smll.200902406.
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods. The spots are observed with a fluorescence scanner. By using the CFM to print spots on nanoporous substrates, an additional order of magnitude increase in signal is observed, which leads to high signal-to-background ratios, highly saturated spots, and a measurable signal at printing concentrations as low as 1.6 ng mL(-1). This technique produces highly concentrated biomolecular spots from dilute samples and significantly increases the sensitivity of sensing platforms.
生物分子,包括蛋白质 A、白蛋白和免疫球蛋白 G,通过使用连续流动微点样器 (CFM) 系统点样到纳米多孔基质上,该系统通常比传统的生物分子打印方法产生的斑点敏感 3 到 4 个数量级。斑点用荧光扫描仪观察。通过使用 CFM 在纳米多孔基质上打印斑点,可以观察到信号增加一个数量级,这导致高信号背景比、高度饱和的斑点和在低至 1.6ng mL(-1)的打印浓度下可测量的信号。该技术从稀释的样品中产生高浓度的生物分子斑点,并显著提高了传感平台的灵敏度。