Fluorescence-Combined Interferometric Scattering Imaging Reveals Nanoscale Dynamic Events of Single Nascent Adhesions in Living Cells

被引:13
|
作者
Park, Jin-Sung [1 ]
Lee, Il-Buem [1 ]
Moon, Hyeon-Min [1 ]
Ryu, Jin-Sun [2 ]
Kong, Sun-Young [3 ]
Hong, Seok-Cheol [1 ,4 ]
Cho, Minhaeng [1 ,5 ]
机构
[1] Inst for Basic Sci Korea, Ctr Mol Spect & Dynam, Seoul 02841, South Korea
[2] Natl Canc Ctr, Ctr Breast Canc, Goyang 10408, South Korea
[3] Natl Canc Ctr, Div Translat Sci, Goyang 10408, South Korea
[4] Korea Univ, Dept Phys, Seoul 02841, South Korea
[5] Korea Univ, Dept Chem, Seoul 02841, South Korea
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2020年 / 11卷 / 23期
关键词
Dynamics; -; Proteins; Interferometry;
D O I
10.1021/acs.jpclett.0c02103
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Focal adhesions (FAs) are dynamic protein nanostructures that form mechanical links between cytoskeletal actin fibers and the extracellular matrix. Here, we demonstrate that interferometric scattering (iSCAT) microscopy, a high-speed and time-unlimited imaging technique, can uncover the real-time dynamics of nanoscopic nascent adhesions (NAs). The high sensitivity and stability of the iSCAT signal enabled us to trace the whole life span of each NA spontaneously nucleated under a lamellipodium. Such high-throughput and long-term image data provide a unique opportunity for statistical analysis of adhesion dynamics. Moreover, we directly revealed that FAs play critical roles in both the extrusion of filopodia as nucleation sites on the leading edge and the one-dimensional transport of cargos along cytoskeletal fibers as fiber docking sites. These experimental results show that iSCAT is a sensitive tool for tracking real-time dynamics of nanoscopic objects involved in endogenous and exogenous biological processes in living cells.
引用
收藏
页码:10233 / 10241
页数:9
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