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Label-Free Nanometer-Resolution Imaging of Biological Architectures through Surface Enhanced Raman Scattering

机译:通过表面增强拉曼散射的生物体系结构的无标签纳米分辨率成像

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摘要

Label free imaging of the chemical environment of biological specimens would readily bridge the supramolecular and the cellular scales, if a chemical fingerprint technique such as Raman scattering can be coupled with super resolution imaging. We demonstrate the possibility of label-free super-resolution Raman imaging, by applying stochastic reconstruction to temporal fluctuations of the surface enhanced Raman scattering (SERS) signal which originate from biomolecular layers on large-area plasmonic surfaces with a high and uniform hot-spot density (>1011/cm2, 20 to 35 nm spacing). A resolution of 20 nm is demonstrated in reconstructed images of self-assembled peptide network and fibrilated lamellipodia of cardiomyocytes. Blink rate density is observed to be proportional to the excitation intensity and at high excitation densities (>10 kW/cm2) blinking is accompanied by molecular breakdown. However, at low powers, simultaneous Raman measurements show that SERS can provide sufficient blink rates required for image reconstruction without completely damaging the chemical structure.
机译:如果可以将化学指纹技术(如拉曼散射)与超分辨率成像结合使用,则生物样品化学环境的无标记成像将很容易在超分子和细胞尺度上架起桥梁。我们通过对表面增强拉曼散射(SERS)信号的时间波动应用随机重建来证明无标签超分辨率拉曼成像的可能性,该信号起因于具有高且均匀热点的大面积等离子体表面上的生物分子层密度(> 10 11 / cm 2 ,间距为20至35 nm)。在自组装肽网络和心肌细胞原纤维化纤网膜脂蛋白的重建图像中显示了20 nm的分辨率。观察到眨眼速率密度与激发强度成正比,在高激发密度(> 10 kW / cm 2 )下,闪烁伴随分子分解。但是,在低功率下,同时进行的拉曼测量表明SERS可以提供​​图像重建所需的足够的闪烁速率,而不会完全损坏化学结构。

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