共 109 条
Investigating the morphological dynamics of the plasma membrane by high-speed atomic force microscopy
被引:5
作者:

Yu, Yiming
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h-index: 0
机构:
Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan

Yoshimura, Shige H.
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h-index: 0
机构:
Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan
机构:
[1] Kyoto Univ, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan
基金:
日本学术振兴会;
关键词:
High-speed atomic force microscopy;
Live-cell imaging;
Clathrin-mediated endocytosis;
Cortical actin;
CLATHRIN-MEDIATED ENDOCYTOSIS;
IN-VIVO DYNAMICS;
ACTIN CYTOSKELETON;
CONFORMATIONAL-CHANGES;
STRESS FIBERS;
CELL-SURFACE;
PROTEINS;
VISUALIZATION;
MECHANISM;
CORTEX;
D O I:
10.1242/jcs.243584
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Despite numerous recent developments in bioimaging techniques, nanoscale and live-cell imaging of the plasma membrane has been challenging because of the insufficient z-resolution of optical microscopes, as well as the lack of fluorescent probes to specifically label small membrane structures. High-speed atomic force microscopy (HS-AFM) is a powerful tool for visualising the dynamics of a specimen surface and is therefore suitable for observing plasma membrane dynamics. Recent developments in HS-AFM for live-cell imaging have enabled the visualisation of the plasma membrane and the network of cortical actin underneath the membrane in a living cell. Furthermore, correlative imaging with fluorescence microscopy allows for the direct visualisation of morphological changes of the plasma membrane together with the dynamic assembly or disassembly of proteins during the entire course of endocytosis in a living cell. Here, we review these recent advances in HS-AFM in order to analyse various cellular events occurring at the cell surface.
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页数:11
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