显微镜
量子点
透射电子显微镜
荧光显微镜
扫描共焦电子显微镜
电子显微镜
扫描透射电子显微镜
荧光
材料科学
分辨率(逻辑)
荧光寿命成像显微镜
扫描电子显微镜
分析化学(期刊)
纳米技术
化学
光学
物理
色谱法
人工智能
计算机科学
复合材料
作者
Madeline J. Dukes,Diana B. Peckys,Niels de Jonge
出处
期刊:ACS Nano
[American Chemical Society]
日期:2010-06-15
卷期号:4 (7): 4110-4116
被引量:85
摘要
Correlative fluorescence microscopy and transmission electron microscopy (TEM) is a state-of-the-art microscopy methodology to study cellular function, combining the functionality of light microscopy with the high resolution of electron microscopy. However, this technique involves complex sample preparation procedures due to its need for either thin sections or frozen samples for TEM imaging. Here, we introduce a novel correlative approach capable of imaging whole eukaryotic cells in liquid with fluorescence microscopy and with scanning transmission electron microscopy (STEM); there is no additional sample preparation necessary for the electron microscopy. Quantum dots (QDs) were bound to epidermal growth factor (EGF) receptors of COS7 fibroblast cells. Fixed whole cells in saline water were imaged with fluorescence microscopy and subsequently with STEM. The STEM images were correlated with fluorescence images of the same cellular regions. QDs of dimensions 7 × 12 nm were visible in a 5 μm thick layer of saline water, consistent with calculations. A spatial resolution of 3 nm was achieved on the QDs.
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