Ren Jinhan, Han Kyu Young
CREOL, The College of Optics and Photonics, University of Central Florida, Orlando, Florida 32816, United States.
ACS Photonics. 2021 Mar 17;8(3):933-942. doi: 10.1021/acsphotonics.1c00012. Epub 2021 Feb 25.
Imaging-based single-cell analysis is essential to study the expression level and functions of biomolecules at subcellular resolution. However, its low throughput has prevented the measurement of numerous cellular features from multiples cells in a rapid and efficient manner. Here we report 2.5D microscopy that significantly improves the throughput of fluorescence imaging systems while maintaining high-resolution and single-molecule sensitivity. Instead of sequential z-scanning, volumetric information is projected onto a 2D image plane in a single shot by engineering the emitted fluorescence light. Our approach provides an improved imaging speed and uniform focal response within a specific imaging depth, which enabled us to perform quantitative single-molecule RNA measurements over a 2×2 mm region within an imaging depth of ~5 μm for mammalian cells in <10 min and immunofluorescence imaging at a >30 Hz volumetric frame rate with reduced photobleaching. Our microscope also offers the ability of multi-color imaging, depth control and super-resolution imaging.
基于成像的单细胞分析对于在亚细胞分辨率下研究生物分子的表达水平和功能至关重要。然而,其低通量阻碍了以快速有效的方式对多个细胞的众多细胞特征进行测量。在此,我们报告了一种2.5D显微镜技术,该技术在保持高分辨率和单分子灵敏度的同时,显著提高了荧光成像系统的通量。通过对发射的荧光进行处理,体积信息不是通过顺序z扫描,而是在单次拍摄中投影到二维图像平面上。我们的方法在特定成像深度内提供了更高的成像速度和均匀的焦平面响应,这使我们能够在不到10分钟的时间内对哺乳动物细胞在约5μm的成像深度内的2×2mm区域进行定量单分子RNA测量,并以大于30Hz的体积帧率进行免疫荧光成像,同时减少光漂白。我们的显微镜还具备多色成像、深度控制和超分辨率成像的能力。