A Labeling Strategy for Living Specimens in Long-Term/Super-Resolution Fluorescence Imaging.
A Labeling Strategy for Living Specimens in Long-Term/Super-Resolution Fluorescence Imaging.
复制标题
长期/超分辨率荧光成像中活体标本的标记策略
DOI:
10.3389/fchem.2020.601436
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发表时间:
2020
影响因子:
5.5
通讯作者:
Hao X
中科院分区:
文献类型:
--
作者:
Han Y;Zhang Z;Liu W;Yao Y;Xu Y;Liu X;Kuang C;Hao X
Despite the urgent need to image living specimens for cutting-edge biological research, most existing fluorescent labeling methods suffer from either poor optical properties or complicated operations required to realize cell-permeability and specificity. In this study, we introduce a method to overcome these limits—taking advantage of the intrinsic affinity of bright and photostable fluorophores, no matter if they are supposed to be live-cell incompatible or not. Incubated with living cells and tissues in particular conditions (concentration and temperature), some Atto and BODIPY dyes show live-cell labeling capability for specific organelles without physical cell-penetration or chemical modifications. Notably, by using Atto 647N as a live-cell mitochondrial marker, we obtain 2.5-time enhancement of brightness and photostability compared with the most commonly used SiR dye in long-term imaging. Our strategy has expanded the scientist's toolbox for understanding the dynamics and interactions of subcellular structures in living specimens.
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影响因子:
16.2
作者:
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通讯作者:
CORY, JG
影响因子:
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