干涉测量
小型化
等离子体子
材料科学
超细纤维
光纤
消散波
分子结合
纳米技术
光学现象
散射
纳米尺度
光学
波长
分子生物物理学
微流控
联轴节(管道)
拉曼散射
干扰(通信)
声波
分布式声传感
光电子学
光学物理学
光散射
光学力
生物成像
纳米光子学
表面等离子共振
生物光子学
物理
纳米流体学
光子学
近场和远场
作者
G Li,Xiaotian Tan,G Wang,Yao Peng,Liu Y,Zhonghao Li,Zhihan Cai,X Y Yang,Yuan Gong,Chaoyang Gong,Tao Zhu
标识
DOI:10.1021/acsphotonics.6c00760
摘要
Direct observation of individual biomolecular events offers mechanistic insights into biological processes and provides a powerful tool for early disease diagnosis. However, the fundamental scale mismatch between optical wavelengths and molecules restricts the application of label-free techniques, leading to a poor signal-to-noise ratio (SNR). Here, we propose a high-contrast, label-free approach based on interferometric imaging, utilizing the strong evanescent field supported on a microfiber surface to provide near-field illumination. We observed unique interference patterns generated by in-plane scattering from natural defects, which enabled the high-contrast detection of localized phase changes induced by single molecules. The results indicate an approximately 38 dB enhancement in the SNR over the conventional fluorescence methods without employing any plasmonic or microcavity-based amplification techniques. This approach was further applied to track molecular dynamics, capturing both the conformational transition and binding behaviors of individual protein molecules. Meanwhile, the stimulus response of single molecules to acoustic waves was investigated, demonstrating the ultimate miniaturization of an acoustic sensor at the single-molecule scale. By enabling direct observation of molecular dynamics and mechanical responses at the single-molecule level, this approach provides a versatile platform for probing fundamental biological processes and developing ultrasensitive biosensors. Moreover, this approach lays the foundation for coupling optical and acoustic waves on the molecular scale, opening new avenues for next-generation single-molecule diagnostics and molecular physics studies.
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