Pilevar S, Davis C C, Portugal F
Bragg Grating Technologies, 3M Specialty Optical Fibers, Bloomfield, Connecticut 06002-1331, USA.
Anal Chem. 1998 May 15;70(10):2031-7. doi: 10.1021/ac9709965.
We present an all-fiber hybridization assay sensor that relies on the evanescent field excitation of fluorescence from surface-bound fluorophores. The evanescent field is made accessible through the use of a long, adiabatically tapered single-mode fiber probe. A laser diode with a 785-nm wavelength is used in a pulsed mode of operation to excite fluorescence in the tapered region of a fiber probe using the near-infrared fluorophore IRD 41. We have used various chemical treatments to prepare the tapered fiber surface for chemical, as well as physical, binding of fluorophores. We have carried out real-time hybridization tests for IRD 41-labeled oligonucleotide, at various probe concentrations, binding to complementary oligonucleotide cross-linked to the tapered fiber surface. The biospecificity of our sensor is confirmed through hybridization tests with a control oligonucleotide. Short oligonucleotides (20-mer) bound to the fiber surface have been used to detect near-IR dye-labeled complementary sequences at subnanomolar levels. Sandwich assays with Helicobacter pylori total RNA were conducted to examine the capability of the biosensor for detecting bacterial cells using rRNA as the target. The results indicate that this fluorosensor is capable of detecting H. pylori in a sandwich assay at picomolar concentrations.
我们展示了一种全光纤杂交检测传感器,该传感器依赖于表面结合荧光团的荧光的倏逝场激发。通过使用一根长的、绝热锥形单模光纤探头,可以获得倏逝场。使用波长为785 nm的激光二极管以脉冲操作模式激发光纤探头锥形区域中的荧光,使用近红外荧光团IRD 41。我们采用了各种化学处理方法来制备锥形光纤表面,以便荧光团进行化学和物理结合。我们对IRD 41标记的寡核苷酸在各种探针浓度下与交联到锥形光纤表面的互补寡核苷酸的结合进行了实时杂交测试。通过与对照寡核苷酸的杂交测试证实了我们传感器的生物特异性。结合到光纤表面的短寡核苷酸(20聚体)已被用于检测亚纳摩尔水平的近红外染料标记的互补序列。进行了幽门螺杆菌总RNA的夹心分析,以检查该生物传感器以rRNA为靶标检测细菌细胞的能力。结果表明,这种荧光传感器能够在夹心分析中检测皮摩尔浓度的幽门螺杆菌。