在水中使用总内部反射尖端增强拉曼光谱学对粉样纤维的纳米级化学成像.
Yuhan Huang1, Gary S Cooney1, David Talaga1
1Univ. Bordeaux, CNRS, Bordeaux INP, ISM, UMR 5255, F-33400 Talence, France.
The journal of physical chemistry letters
|October 1, 2024
概括
总内部反射尖增强拉曼光谱 (TIR-TERS) 揭示了水中的粉样β纤维结构. 补水对纤维结构的影响最小,开辟了新的生物成像可能性.
科学领域:
- 生物物理学的生物物理.
- 频谱学是一种光谱学.
- 材料科学 材料科学 材料科学
背景情况:
- 粉样β纤维素与神经退行性疾病有关.
- 了解它们在生物相关环境中的结构至关重要.
- 以前的研究仅限于环境空气条件.
研究的目的:
- 使用TIR-TERS. 在水中进行粉样β (Aβ1-42-L34T) 纤维的纳米尺度成像.
- 为了研究水分对粉样纤维结构的影响.
- 为了探索芳香氨基酸在纤维中的分布.
主要方法:
- 通过双极电位定位制造TERS尖端.
- 总内部反射尖增强拉曼光谱 (TIR-TERS) 在水溶液中的成像.
- 理论模拟以优化实验参数.
主要成果:
- 在水中实现的Aβ1-42-L34T纤维的纳米空间分辨率成像.
- 确定了占主导地位的平行β片次要结构.
- 图中显示了氨酸,氨酸和氨酸的纳米分布.
- 证明水化对纤维结构有边际影响.
结论:
- TIR-TERS是一种可行的技术,用于研究液体中的粉样纤维.
- 粉样纤维的结构在水性环境中在很大程度上得到保存.
- 这项研究为TIR-TERS的未来生物应用提供了基础.
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Imaging Biological Samples with Optical Microscopy
Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
Total Internal Reflection Fluorescence Microscopy
Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
Super-resolution Fluorescence Microscopy
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been developed.


