Biomolecular Nanotechnology Center, Department of Bioengineering, University of California, Berkeley, California 94720, USA.
Lab Chip. 2009 Dec 7;9(23):3360-3. doi: 10.1039/b912076a. Epub 2009 Oct 1.
In this paper, we present a method combining surface-enhanced Raman scattering (SERS) spectroscopy to detect biomolecules in a label-free way with an electrokinetic preconcentration technique (electrophoresis) to amplify biomolecular signals at low concentrations. A constant electric field is applied to charged biomolecules in solution, attracting them to an oppositely charged electrode, which is also used as a SERS substrate. Within 5 min, we observed that the SERS signal of 10 fM adenine was amplified to the level of the signal of non-preconcentrated 1 microM adenine (sensitivity improvement by 8 orders of magnitude) and the method was effective over a wide range of concentrations (10 fM to 1 microM). The signals were further amplified under stronger electric field and longer application: The increase of the signal intensity was observed to be 51 times at -0.6 V cm(-1) after 25 min. The effectiveness of this method allows the creation of label-free, target-specific, and highly sensitive monitoring applications.
在本文中,我们提出了一种将表面增强拉曼散射(SERS)光谱学与无标记的电动力学预浓缩技术(电泳)相结合的方法,用于在低浓度下放大生物分子信号。在溶液中,施加恒定电场会吸引带电荷的生物分子到带相反电荷的电极,该电极也可用作 SERS 基底。在 5 分钟内,我们观察到 10 fM 腺嘌呤的 SERS 信号被放大到非浓缩的 1 microM 腺嘌呤信号水平(灵敏度提高了 8 个数量级),并且该方法在很宽的浓度范围内有效(10 fM 至 1 microM)。在更强的电场和更长的应用时间下,信号得到进一步放大:在 -0.6 V cm(-1) 下 25 分钟后,观察到信号强度增加了 51 倍。该方法的有效性允许创建无标记、靶向和高灵敏度的监测应用。