Yin Jiaze, Zhang Meng, Tan Yuying, Guo Zhongyue, He Hongjian, Lan Lu, Cheng Ji-Xin
bioRxiv. 2023 Mar 1:2023.02.27.530116. doi: 10.1101/2023.02.27.530116.
By optically sensing the mid-infrared absorption induced photothermal effect, midinfrared photothermal (MIP) microscope enables super-resolution IR imaging and scrutinizing of biological systems in an aqueous environment. However, the speed of current lock-in based sample-scanning MIP system is limited to 1.0 millisecond or longer per pixel, which is insufficient for capturing dynamics inside living systems. Here, we report a single pulse laserscanning MIP microscope that dramatically increases the imaging speed by three orders of magnitude. We harness a lock-in free demodulation scheme which uses high-speed digitization to resolve single IR pulse induced contrast at nanosecond time scale. To realize single pulse photothermal detection at each pixel, we employ two sets of galvo mirrors for synchronized scanning of mid-infrared and probe beams to achieve an imaging line rate over 2 kHz. With video-rate imaging capability, we observed two types of distinct dynamics of lipids in living cells. Furthermore, by hyperspectral imaging, we chemically dissected a single cell wall at nanometer scale. Finally, with a uniform field of view over 200 by 200 μm and 2 Hz frame rate, we mapped fat storage in free-moving and live embryos.
通过光学检测中红外吸收诱导的光热效应,中红外光热(MIP)显微镜能够在水环境中对生物系统进行超分辨率红外成像和细致观察。然而,当前基于锁相放大器的样品扫描MIP系统的速度限制为每像素1.0毫秒或更长时间,这不足以捕捉生命系统内部的动态过程。在此,我们报道了一种单脉冲激光扫描MIP显微镜,其成像速度显著提高了三个数量级。我们采用了一种无需锁相放大器的解调方案,该方案利用高速数字化技术在纳秒时间尺度上解析单个红外脉冲诱导的对比度。为了在每个像素处实现单脉冲光热检测,我们使用两组振镜对中红外光束和探测光束进行同步扫描,以实现超过2 kHz的成像线速率。凭借视频速率成像能力,我们观察到了活细胞中两种不同类型的脂质动态。此外,通过高光谱成像,我们在纳米尺度上对单个细胞壁进行了化学剖析。最后,在200×200μm的均匀视场和2 Hz的帧率下,我们绘制了自由移动的活胚胎中的脂肪储存情况。