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采用单光子雪崩二极管阵列的光片自发荧光寿命成像

Light sheet autofluorescence lifetime imaging with a single photon avalanche diode array.

作者信息

Samimi Kayvan, Desa Danielle E, Lin Wei, Weiss Kurt, Li Joe, Huisken Jan, Miskolci Veronika, Huttenlocher Anna, Chacko Jenu V, Velten Andreas, Rogers Jeremy D, Eliceiri Kevin W, Skala Melissa C

机构信息

Morgridge Institute for Research, Madison, WI, USA.

Department of Electrical and Computer Engineering, University of Wisconsin, Madison, WI, USA.

出版信息

bioRxiv. 2023 Feb 3:2023.02.01.526695. doi: 10.1101/2023.02.01.526695.

Abstract

Single photon avalanche diode (SPAD) array sensors can increase the imaging speed for fluorescence lifetime imaging microscopy (FLIM) by transitioning from laser scanning to widefield geometries. While a SPAD camera in epi-fluorescence geometry enables widefield FLIM of fluorescently labeled samples, label-free imaging of single-cell autofluorescence is not feasible in an epi-fluorescence geometry because background fluorescence from out-of-focus features masks weak cell autofluorescence and biases lifetime measurements. Here, we address this problem by integrating the SPAD camera in a light sheet illumination geometry to achieve optical sectioning and limit out-of-focus contributions, enabling fast label-free FLIM of single-cell NAD(P)H autofluorescence. The feasibility of this NAD(P)H light sheet FLIM system was confirmed with time-course imaging of metabolic perturbations in pancreas cancer cells with 10 s integration times, and NAD(P)H light sheet FLIM was demonstrated with live neutrophil imaging in a zebrafish tail wound, also with 10 s integration times. Finally, the theoretical and practical imaging speeds for NAD(P)H FLIM were compared across laser scanning and light sheet geometries, indicating a 30X to 6X frame rate advantage for the light sheet compared to the laser scanning geometry. This light sheet system provides faster frame rates for 3D NAD(P)H FLIM for live cell imaging applications such as monitoring single cell metabolism and immune cell migration throughout an entire living organism.

摘要

单光子雪崩二极管(SPAD)阵列传感器可以通过从激光扫描转换为宽场几何结构来提高荧光寿命成像显微镜(FLIM)的成像速度。虽然落射荧光几何结构中的SPAD相机能够对荧光标记样本进行宽场FLIM成像,但在落射荧光几何结构中,单细胞自发荧光的无标记成像并不可行,因为离焦特征产生的背景荧光会掩盖微弱的细胞自发荧光,并使寿命测量产生偏差。在此,我们通过将SPAD相机集成到光片照明几何结构中来解决这一问题,以实现光学切片并限制离焦贡献,从而实现单细胞NAD(P)H自发荧光的快速无标记FLIM成像。通过对胰腺癌细胞代谢扰动进行10秒积分时间的时间进程成像,证实了这种NAD(P)H光片FLIM系统的可行性,并且在斑马鱼尾部伤口的活中性粒细胞成像中也展示了NAD(P)H光片FLIM,同样采用10秒积分时间。最后,比较了激光扫描和光片几何结构下NAD(P)H FLIM的理论和实际成像速度,结果表明与激光扫描几何结构相比,光片的帧率优势为30倍至6倍。这种光片系统为活细胞成像应用(如监测整个生物体中的单细胞代谢和免疫细胞迁移)的3D NAD(P)H FLIM提供了更快的帧率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3222/9915663/2104fec28c7d/nihpp-2023.02.01.526695v1-f0001.jpg

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