具有可调节折射率的超软凝用于力显微镜
J Zsolt Terdik1, David A Weitz1,2,3, Frans Spaepen1
1John A. Paulson School of Engineering and Applied Sciences, Harvard University, 9 Oxford Street, Cambridge, MA 02138, USA. terdik@g.harvard.edu.
Soft matter
|May 31, 2024
概括
研究人员开发了新的凝,具有可调节的折射率,用于力显微镜. 这些凝通过将光学偏差最小化,使更敏感的应力测量和更清晰的成像成为可能.
科学领域:
- 生物物理学的生物物理.
- 材料科学 材料科学 材料科学
- 软物质物理学 软物质物理学
背景情况:
- 引力显微镜 (TFM) 需要明确的基质特性来准确地测量细胞力学.
- 现有的TFM基板经常受到光学偏差的影响,对低应力敏感性有限.
研究的目的:
- 为先进的TFM应用程序制定和描述具有可调节光学和机械性能的凝.
- 通过尽量减少光学扭曲来提高TFM的灵敏度和图像质量.
主要方法:
- 在凝门附近,用受控的粘弹性模块 (G'~1Pa) 制备凝.
- 调整折射率 (1.4 < n < 1.49) 以匹配成像目标并减少球形偏差.
- 开发索引匹配的合性颗粒用于内部凝变形跟踪.
主要成果:
- 凝显示低频存储高原模块在50Pa和1Pa之间,损失模块超过50倍低.
- 保持直线弹性高达50%的拉伸,确保精确的变形测量.
- 折射率调整成功地消除了球形偏差,从而改善了对焦成像.
结论:
- 开发的近临界凝提供了可调节光学和机械性能的独特组合.
- 这些凝显著提高了TFM能力,将应力检测极限扩展到毫帕斯卡范围.
- 优化的凝和粒子探针为研究细胞力学提供了强大的工具,具有前所未有的精度.
相关概念视频
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.


