分辨率(逻辑)
荧光寿命成像显微镜
荧光
计算机科学
人工智能
光学
物理
作者
Hai‐Hao Han,Xiaopeng He
出处
期刊:Royal Society of Chemistry eBooks
[The Royal Society of Chemistry]
日期:2024-10-31
卷期号:: 71-103
标识
DOI:10.1039/9781837673117-00071
摘要
Our current understanding of living systems has advanced to the level of individual cells. However, there is still a pressing need to more precisely visualize the microstructure of cells, as well as the dynamic actions of biomolecules therein, including molecular translocation and chemical modifications (e.g. epigenetics and post-translational modification) at the molecular level in real time. Fluorescence microscopy permits non-invasive imaging of biomolecules in living cells, but its resolution is limited by diffraction. While electron microscopy provides a higher resolution, it requires fixed cells to be used, thus compromising the fidelity of the structural and functional information of biomacromolecules. Super-resolution fluorescence microscopy (SRFM) has emerged as a groundbreaking technology that addresses the diffraction limit issue, and enables high-resolution imaging of subcellular as well as biomolecular structures. The advent of SRFM has significantly advanced our understanding of how cellular structures are exquisitely organized, and how biomolecules interact with each other to modulate cell fate. This chapter will discuss the recent progress in the use of various SRFM-based techniques for the structural and functional imaging of cells. The diverse fluorescent agents developed for SRFMs will also be summarized.
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