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使用二维金纳米粒子薄片对细胞附着纳米界面进行高分辨率成像。

High-resolution imaging of a cell-attached nanointerface using a gold-nanoparticle two-dimensional sheet.

机构信息

Institute for Materials Chemistry and Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.

Graduate School of Biomedical & Health Science, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima City Hiroshima, 734-8553, Japan.

出版信息

Sci Rep. 2017 Jun 16;7(1):3720. doi: 10.1038/s41598-017-04000-4.

Abstract

This paper proposes a simple, effective, non-scanning method for the visualization of a cell-attached nanointerface. The method uses localized surface plasmon resonance (LSPR) excited homogeneously on a two-dimensional (2D) self-assembled gold-nanoparticle sheet. The LSPR of the gold-nanoparticle sheet provides high-contrast interfacial images due to the confined light within a region a few tens of nanometers from the particles and the enhancement of fluorescence. Test experiments on rat basophilic leukemia (RBL-2H3) cells with fluorescence-labeled actin filaments revealed high axial and lateral resolution even under a regular epifluorescence microscope, which produced higher quality images than those captured under a total internal reflection fluorescence (TIRF) microscope. This non-scanning-type, high-resolution imaging method will be an effective tool for monitoring interfacial phenomena that exhibit relatively rapid reaction kinetics in various cellular and molecular dynamics.

摘要

本文提出了一种简单、有效、非扫描的方法,用于可视化细胞附着的纳米界面。该方法利用二维(2D)自组装金纳米粒子片上均匀激发的局域表面等离子体共振(LSPR)。由于光被限制在距离粒子几十纳米的区域内,并且荧光得到增强,因此金纳米粒子片的 LSPR 提供了高对比度的界面图像。使用荧光标记的肌动蛋白丝对大鼠嗜碱性白血病(RBL-2H3)细胞进行的测试实验表明,即使在常规明场显微镜下,也具有高轴向和侧向分辨率,其产生的图像质量高于全内反射荧光(TIRF)显微镜捕获的图像。这种非扫描式、高分辨率成像方法将成为监测各种细胞和分子动力学中具有相对快速反应动力学的界面现象的有效工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ded7/5473937/0865afe4d571/41598_2017_4000_Fig1_HTML.jpg

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