Steinbach Gabor, Nagy David, Sipka Gábor, Manders Erik, Garab Győző, Zimányi László
Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Temesvári krt. 62, Szeged, 6726, Hungary.
Institute of Plant Biology, Biological Research Centre, Hungarian Academy of Sciences, Temesvári krt. 62, Szeged, 6726, Hungary.
Eur Biophys J. 2019 Jul;48(5):457-463. doi: 10.1007/s00249-019-01365-4. Epub 2019 Apr 13.
Confocal laser scanning microscopy is probably the most widely used and one of the most powerful techniques in basic biology, medicine and material sciences that is employed to elucidate the architecture of complex cellular structures and molecular macro-assemblies. It has recently been shown that the information content, signal-to-noise ratio and resolution of such microscopes (LSMs) can be improved significantly by adding different attachments or modifying their design, while retaining their user-friendly features and relatively moderate costs. Differential polarization (DP) attachments, using high-frequency modulation/demodulation circuits, have made LSMs capable of high-precision 2D and 3D mapping of the anisotropy of microscopic samples-without interfering with their 'conventional' fluorescence or transmission imaging (Steinbach et al. in Methods Appl Fluoresc 2:015005, 2014). The resolution and the quality of fluorescence imaging have been enhanced in the recently constructed Re-scan confocal microscopy (RCM) (De Luca et al. in Biomed Opt Express 4:2644-2656, 2013). In this work, we developed the RCM technique further, by adding a DP-attachment modulating the exciting laser beam via a liquid crystal (LC) retarder synchronized with the data acquisition system; by this means, and with the aid of a software, fluorescence-detected linear dichroism (FDLD), characteristic of the anisotropic molecular organization of the sample, could be recorded in parallel with the confocal fluorescence imaging. For demonstration, we show FDLD images of a plant cell wall (Ginkgo biloba) stained with Etzold's staining solution.
共聚焦激光扫描显微镜可能是基础生物学、医学和材料科学中使用最广泛且功能最强大的技术之一,用于阐明复杂细胞结构和分子宏观组装体的结构。最近的研究表明,通过添加不同附件或改进设计,此类显微镜(激光扫描显微镜,LSM)的信息含量、信噪比和分辨率可显著提高,同时保留其用户友好特性和相对适中的成本。使用高频调制/解调电路的差分偏振(DP)附件使LSM能够对微观样品的各向异性进行高精度二维和三维映射,而不会干扰其“传统”荧光或透射成像(斯坦巴赫等人,《方法与应用荧光》2:015005,2014年)。在最近构建的再扫描共聚焦显微镜(RCM)中,荧光成像的分辨率和质量得到了提高(德卢卡等人,《生物医学光学快报》4:2644 - 2656,2013年)。在这项工作中,我们进一步开发了RCM技术,通过添加一个DP附件,该附件通过与数据采集系统同步的液晶(LC)延迟器调制激发激光束;通过这种方式,并借助软件,可以在共聚焦荧光成像的同时记录样品各向异性分子组织特有的荧光检测线性二色性(FDLD)。为了演示,我们展示了用埃佐尔德染色液染色的植物细胞壁(银杏)的FDLD图像。