Munge Bernard, Liu Guodong, Collins Greg, Wang Joseph
Department of Chemical and Materials Engineering, Biodesign Institute, Arizona State University, Tempe, Arizona 85287-5001, USA.
Anal Chem. 2005 Jul 15;77(14):4662-6. doi: 10.1021/ac050132g.
Signal amplification using enzyme multilayers on carbon nanotube (CNT) templates is shown to yield a remarkably sensitive electrochemical detection of proteins and nucleic acids. The electrostatic layer-by-layer (LBL) self-assembly onto CNT carriers maximizes the ratio of enzyme tags per binding event to offer the greatest amplification factor reported to date. Absorption spectroscopy, TEM, and electrochemical characterization confirm the formation of LBL enzyme nanostructures on individual CNT carriers. The enzymatic activity is found to increase with the number of enzyme layers. The new protocol is illustrated for monitoring sandwich hybridization and antibody-antigen interactions in connection with alkaline phosphatase tracers. Factors affecting the enzyme loading and the analytical performance have been optimized. Such amplified bioelectronic assays allow detection of DNA and proteins down to 80 copies (5.4 aM) and 2000 protein molecules (67 aM), respectively. Given the enormous amplification afforded by the new CNT-LBL biolabel, such route offers great promise for ultrasensitive detection of infectious agents and disease markers.
研究表明,在碳纳米管(CNT)模板上使用酶多层进行信号放大,能够实现对蛋白质和核酸的超高灵敏度电化学检测。通过静电逐层(LBL)自组装到CNT载体上,可使每次结合事件中酶标记物的比例最大化,从而提供了迄今为止报道的最大放大倍数。吸收光谱、透射电子显微镜(TEM)和电化学表征证实了在单个CNT载体上形成了LBL酶纳米结构。研究发现酶活性随酶层数增加而提高。本文通过与碱性磷酸酶示踪剂相关的夹心杂交和抗体-抗原相互作用监测,展示了这种新方法。对影响酶负载量和分析性能的因素进行了优化。这种放大的生物电子检测方法能够分别检测低至80个拷贝(5.4 aM)的DNA和2000个蛋白质分子(67 aM)。鉴于新型CNT-LBL生物标记物具有巨大的放大作用,这种方法在超灵敏检测传染病原体和疾病标志物方面具有广阔前景。