Department of Chemistry , University of Washington , Seattle , Washington 98195 , United States.
J Phys Chem B. 2019 Oct 10;123(40):8397-8404. doi: 10.1021/acs.jpcb.9b07075. Epub 2019 Sep 27.
Stimulated Raman scattering (SRS) microscopy is a powerful method for imaging molecular distributions based on their intrinsic vibrational contrast. However, despite a growing list of biological applications, SRS is frequently hindered by a parasitic background signal which both overpowers the signal in low-signal applications and makes the extraction of quantitative information from images challenging. Frequency modulation (FM) has been used to suppress this parasitic background. However, many FM-SRS methods require either the acquisition of multiple images or the addition of multiple optomechanical components and an extensive realignment procedure. Herein, we report a new procedure for alignment-free FM-SRS utilizing polarization encoding. We demonstrate the efficacy of this approach, along with parabolic amplification of the Stokes pulse, at removing parasitic background signals in SRS microscopy applications. We further highlight how this technique can be used to suppress Raman signals from major molecular species to unveil spectral signatures from nucleic acids in both murine brain tissue and whole blood. Due to its ease of use and demonstrated experimental capabilities, we expect this technique to see broad use in the SRS microscopy community.
受激拉曼散射(SRS)显微镜是一种基于分子固有振动对比度成像的强大方法。然而,尽管 SRS 在生物学中有越来越多的应用,但它经常受到寄生背景信号的阻碍,这种信号在低信号应用中会压倒信号,并使得从图像中提取定量信息具有挑战性。频率调制(FM)已被用于抑制这种寄生背景。然而,许多 FM-SRS 方法要么需要采集多个图像,要么需要添加多个光机械组件和一个广泛的重新调整程序。在这里,我们报告了一种利用偏振编码进行无对准 FM-SRS 的新程序。我们演示了这种方法以及抛物线放大斯托克斯脉冲在 SRS 显微镜应用中去除寄生背景信号的效果。我们进一步强调了如何利用该技术来抑制主要分子物种的拉曼信号,以揭示来自鼠脑组织和全血中核酸的光谱特征。由于其易于使用和经过验证的实验能力,我们预计该技术将在 SRS 显微镜领域得到广泛应用。