Institute of Pharmaceutical Science, School of Cancer and Pharmaceutical Sciences, King's College London, UK.
Faculty of Sciences, BioISI-Biosystems & Integrative Sciences Institute, University of Lisboa, Lisbon, Portugal.
Appl Spectrosc. 2020 May;74(5):544-552. doi: 10.1177/0003702819898275. Epub 2020 Mar 30.
Fourier transform infrared (FT-IR) spectroscopic imaging and microscopy of single living cells are established label-free technique for the study of cell biology. The constant driver to improve the spatial resolution of the technique is due to the diffraction limit given by infrared (IR) wavelength making subcellular study challenging. Recently, we have reported, with the use of a prototype zinc sulfide (ZnS) transmission cell made of two hemispheres, that the spatial resolution is improved by the factor of the refractive index of ZnS, achieving a λ/2.7 spatial resolution using the synchrotron-IR microscopy with a 36× objective with numerical aperture of 0.5. To refine and to demonstrate that the ZnS hemisphere transmission device can be translated to standard bench-top FT-IR imaging systems, we have, in this work, modified the device to achieve a more precise path length, which has improved the spectral quality of the living cells, and showed for the first time that the device can be applied to study live cells with three different bench-top FT-IR imaging systems. We applied focal plane array (FPA) imaging, linear array, and a synchrotron radiation single-point scanning method and demonstrated that in all cases, subcellular details of individual living cells can be obtained. Results have shown that imaging with the FPA detector can measure the largest area in a given time, while measurements from the scanning methods produced a smoother image. Synchrotron radiation single-point mapping produced the best quality image and has the flexibility to introduce over sampling to produce images of cells with great details, but it is time consuming in scanning mode. In summary, this work has demonstrated that the ZnS hemispheres can be applied in all three spectroscopic approaches to improve the spatial resolution without any modification to the existing microscopes.
傅里叶变换红外(FT-IR)光谱学成像和显微镜技术是研究细胞生物学的一种无标记技术,可用于对单个活细胞进行分析。提高该技术空间分辨率的主要驱动力是由于红外(IR)波长的衍射极限,使得亚细胞研究具有挑战性。最近,我们使用由两个半球组成的硫化锌(ZnS)传输细胞原型,通过 ZnS 的折射率提高了空间分辨率,在具有 36×物镜和 0.5 数值孔径的同步辐射显微镜下,使用 36×物镜和 0.5 数值孔径,实现了 λ/2.7 的空间分辨率。为了改进和证明 ZnS 半球传输装置可以转化为标准台式 FT-IR 成像系统,我们在这项工作中对该装置进行了修改,以实现更精确的光程,从而提高了活细胞的光谱质量,并首次展示了该装置可以应用于三种不同的台式 FT-IR 成像系统研究活细胞。我们应用了焦平面阵列(FPA)成像、线性阵列和同步辐射单点扫描方法,并证明在所有情况下,都可以获得单个活细胞的亚细胞细节。结果表明,使用 FPA 探测器进行成像可以在给定时间内测量最大区域,而扫描方法的测量结果产生更平滑的图像。同步辐射单点映射产生了最佳质量的图像,并且具有灵活性,可以引入过采样,以生成具有更多细节的细胞图像,但扫描模式下耗时较长。总之,这项工作证明了 ZnS 半球可以应用于所有三种光谱方法,在不改变现有显微镜的情况下提高空间分辨率。