High spatiotemporal resolution and low photo-toxicity fluorescence imaging in live cells and in vivo

Author:

Peng Xiaohong12,Huang Xiaoshuai2,Du Ke2,Liu Huisheng1,Chen Liangyi23ORCID

Affiliation:

1. Beijing Advanced Innovation Center for Big Data-Based Precision Medicine, Interdisciplinary Innovation Institute of Medicine and Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing 100191, China

2. State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, Beijing 100871, China

3. PKU-IDG/McGovern Institute for Brain Research, Beijing 100871, China

Abstract

Taking advantage of high contrast and molecular specificity, fluorescence microscopy has played a critical role in the visualization of subcellular structures and function, enabling unprecedented exploration from cell biology to neuroscience in living animals. To record and quantitatively analyse complex and dynamic biological processes in real time, fluorescence microscopes must be capable of rapid, targeted access deep within samples at high spatial resolutions, using techniques including super-resolution fluorescence microscopy, light sheet fluorescence microscopy, and multiple photon microscopy. In recent years, tremendous breakthroughs have improved the performance of these fluorescence microscopies in spatial resolution, imaging speed, and penetration. Here, we will review recent advancements of these microscopies in terms of the trade-off among spatial resolution, sampling speed and penetration depth and provide a view of their possible applications.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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