荧光
细胞质
氨基酸
纳米技术
生物物理学
材料科学
活体细胞成像
光致发光
细胞
化学
光电子学
生物
生物化学
光学
物理
作者
Huai Chen,Jiang Xu,Yaping Wang,Da Wang,Raquel Ferrer‐Espada,Yutong Wang,Jingjian Zhou,Adrián Pedrazo‐Tardajos,Mei Yang,Jia‐Heng Tan,Xiaoyu Yang,Lei Zhang,Ilya Sychugov,Shoudeng Chen,Sara Bals,Johan Paulsson,Zhenyu Yang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-09-15
卷期号:16 (9): 15450-15459
被引量:8
标识
DOI:10.1021/acsnano.2c07443
摘要
Fluorescent probes are vital to cell imaging by allowing specific parts of cells to be visualized and quantified. Color-switchable probes (CSPs), with tunable emission wavelength upon contact with specific targets, are particularly powerful because they not only eliminate the need to wash away all unbound probe but also allow for internal controls of probe concentrations, thereby facilitating quantification. Several such CSPs exist and have proven very useful, but not for all key cellular targets. Here we report a pioneering CSP for in situ cell imaging using aldehyde-functionalized silicon nanocrystals (SiNCs) that switch their intrinsic photoluminescence from red to blue quickly when interacting with amino acids in live cells. Though conventional probes often work better in cell-free extracts than in live cells, the SiNCs display the opposite behavior and function well and fast in universal cell lines at 37 °C while requiring much higher temperature in extracts. Furthermore, the SiNCs only disperse in cytoplasm not nucleus, and their fluorescence intensity correlated linearly with the concentration of fed amino acids. We believe these nanosilicon probes will be promising tools to visualize distribution of amino acids and potentially quantify amino acid related processes in live cells.
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