首页> 外文期刊>ACS applied materials & interfaces >In Situ Monitoring of Rolling Circle Amplification on a Solid Support by Surface Plasmon Resonance and Optical Waveguide Spectroscopy
【24h】

In Situ Monitoring of Rolling Circle Amplification on a Solid Support by Surface Plasmon Resonance and Optical Waveguide Spectroscopy

机译:以表面等离子体谐振和光波导光谱法对固体支持物的滚动圆扩增的原位监测

获取原文
获取原文并翻译 | 示例
       

摘要

The growth of surface-attached single-stranded deoxyribonucleic acid (ssDNA) chains is monitored in situ using an evanescent wave optical biosensor that combines surface plasmon resonance (SPR) and optical waveguide spectroscopy (OWS). The “grafting-from” growth of ssDNA chains is facilitated by rolling circle amplification (RCA), and the gradual prolongation of ssDNA chains anchored to a gold sensor surface is optically tracked in time. At a sufficient density of the polymer chains, the ssDNA takes on a brush architecture with a thickness exceeding 10 μm, supporting a spectrum of guided optical waves traveling along the metallic sensor surface. The simultaneous probing of this interface with the confined optical field of surface plasmons and additional more delocalized dielectric optical waveguide modes enables accurate in situ measurement of the ssDNA brush thickness, polymer volume content, and density gradients. We report for the first time on the utilization of the SPR/OWS technique for the measurement of the RCA speed on a solid surface that can be compared to that in bulk solutions. In addition, the control of ssDNA brush properties by changing the grafting density and ionic strength and post-modification via affinity reaction with complementary short ssDNA staples is discussed. These observations may provide important leads for tailoring RCA toward sensitive and rapid assays in affinity-based biosensors.
机译:使用结合表面等离子体共振(SPR)和光波导光谱(OWS)的倏逝波光学生物传感器,对表面附着的单链脱氧核糖核酸(ssDNA)链的生长进行原位监测。滚动圆扩增(RCA)促进了单链DNA链的“嫁接”生长,并对锚定在金传感器表面的单链DNA链的逐渐延长进行了光学跟踪。当聚合物链密度足够大时,单链DNA呈刷状结构,厚度超过10μm,支持沿金属传感器表面传播的导光波光谱。利用表面等离子体激元的受限光场和其他更非定域的介质光波导模式同时探测该界面,能够准确地原位测量ssDNA刷厚度、聚合物体积含量和密度梯度。我们首次报道了利用SPR/OWS技术测量固体表面上的RCA速度,该速度可与大块溶液中的RCA速度进行比较。此外,还讨论了通过改变接枝密度和离子强度,以及通过与互补短ssDNA片段的亲和反应进行后修饰来控制ssDNA刷子性能的方法。这些观察结果可能为在基于亲和性的生物传感器中调整RCA以实现灵敏和快速的分析提供重要线索。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号