Vollmer Frank, Arnold Stephen, Braun Dieter, Teraoka Iwao, Libchaber Albert
Center for Studies in Physics and Biology, Rockefeller University, New York, New York 10021, USA.
Biophys J. 2003 Sep;85(3):1974-9. doi: 10.1016/S0006-3495(03)74625-6.
We have developed a novel, spectroscopic technique for high-sensitivity, label-free DNA quantification. We demonstrate that an optical resonance (whispering gallery mode) excited in a micron-sized silica sphere can be used to detect and measure nucleic acids. The surface of the silica sphere is chemically modified with oligonucleotides. We show that hybridization to the target DNA leads to a red shift of the optical resonance wavelength. The sensitivity of this resonant technique is measured as 6 pg/mm(2) mass loading, higher as compared to most optical single-pass devices such as surface plasmon resonance biosensors. Furthermore, we show that each microsphere can be identified by its unique resonance wavelength. Specific, multiplexed DNA detection is demonstrated by using two microspheres. The multiplexed signal from two microspheres allows us to discriminate a single nucleotide mismatch in an 11-mer oligonucleotide with a high signal-to-noise ratio of 54. This all-photonic whispering gallery mode biosensor can be integrated on a semiconductor chip that makes it an easy to manufacture, analytic component for a portable, robust lab-on-a-chip device.
我们开发了一种用于高灵敏度、无标记DNA定量的新型光谱技术。我们证明,在微米级二氧化硅球体中激发的光学共振(回音壁模式)可用于检测和测量核酸。二氧化硅球体表面用寡核苷酸进行化学修饰。我们表明,与靶DNA杂交会导致光学共振波长发生红移。这种共振技术的灵敏度测量为6 pg/mm(2) 的质量负载,比大多数光学单通道设备(如表面等离子体共振生物传感器)更高。此外,我们表明每个微球都可以通过其独特的共振波长进行识别。使用两个微球证明了特异性、多重DNA检测。来自两个微球的多重信号使我们能够以54的高信噪比区分11聚体寡核苷酸中的单个核苷酸错配。这种全光子回音壁模式生物传感器可以集成在半导体芯片上,使其成为易于制造的便携式、坚固的芯片实验室设备的分析组件。