Heyduk Ewa, Dummit Benjamin, Chang Yie-Hwa, Heyduk Tomasz
Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University Medical School, 1100 South Grand Boulevard, St. Louis, Missouri 63104, USA.
Anal Chem. 2008 Jul 1;80(13):5152-9. doi: 10.1021/ac8004154. Epub 2008 May 21.
We describe here a new homogeneous antibody-based protein sensor design (molecular pincers) that allows rapid and sensitive detection of a specific protein in solution. In the presence of the target protein these sensors produce fluorescence signal derived from target-dependent annealing of short complementary fluorochrome-labeled oligonucleotides attached to a pair of target-specific antibodies via nanometer-scale flexible linkers. The sensors allow near-instantaneous detection of the target with sensitivity and specificity approaching that of enzyme-linked immunosorbent assay (ELISA) but requiring no sample manipulation other then the addition of the sample to the sensor mix. We used cardiac troponin I and C-reactive protein as the targets to validate these desirable properties of the sensors. Due to the availability of antibodies to thousands of interesting targets and the straightforward design blueprint of the sensors we expect their wide-ranging applications in research and medical diagnosis, especially when simplicity, high throughput, and short detection time are essential.
我们在此描述一种基于抗体的新型均相蛋白质传感器设计(分子钳),它能够快速、灵敏地检测溶液中的特定蛋白质。在目标蛋白质存在的情况下,这些传感器会产生荧光信号,该信号源自通过纳米级柔性接头连接到一对目标特异性抗体上的短互补荧光染料标记寡核苷酸的目标依赖性退火。这些传感器能够近乎即时地检测目标,其灵敏度和特异性接近酶联免疫吸附测定(ELISA),但除了将样品添加到传感器混合物中外,无需进行其他样品处理。我们使用心肌肌钙蛋白I和C反应蛋白作为目标来验证这些传感器的理想特性。由于有成千上万种有趣目标的抗体可供使用,且传感器的设计蓝图简单直接,我们预计它们将在研究和医学诊断中得到广泛应用,特别是在需要简单性、高通量和短检测时间的情况下。