在浑浊食品乳剂中实现单分子定位显微镜。

Abbas Jabermoradi, Suyeon Yang, Martijn I Gobes, John P M van Duynhoven, Johannes Hohlbein
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引用次数: 0

摘要

浊度对食物系统的微观表征提出了重大挑战。例如,折射率的局部不匹配会导致沿样品深度的显著图像劣化。为了缓解浊度问题并提高食品显微镜的光学分辨率,我们在之前发布的开放显微镜框架miCube中添加了自适应光学(AO)和平场照明。在检测路径中,我们通过一个可变形反射镜实现AO,以补偿像差和调制发射波前,从而实现单分子定位显微镜(SMLM)三维点扩展函数(psf)的工程。作为非透明食品胶体(如蛋黄酱)的模型系统,我们设计了一种含有蛋黄中常见的铁离子结合蛋白磷维素的水包油乳液。我们用荧光标记的一抗靶向phosvitin,并利用PSF工程获得了分辨率为亚100nm的phosvitin覆盖油滴的二维和三维图像。我们的数据表明,光维素在界面上均匀分布。由于有可能获得深度的超分辨率图像,我们的工作为在食品乳剂的异质胶体界面上定位生物大分子铺平了道路。本文是Theo Murphy会议议题“超分辨率结构照明显微镜(第二部分)”的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enabling single-molecule localization microscopy in turbid food emulsions.

Turbidity poses a major challenge for the microscopic characterization of food systems. Local mismatches in refractive indices, for example, lead to significant image deterioration along sample depth. To mitigate the issue of turbidity and to increase the accessible optical resolution in food microscopy, we added adaptive optics (AO) and flat-field illumination to our previously published open microscopy framework, the miCube. In the detection path, we implemented AO via a deformable mirror to compensate aberrations and to modulate the emission wavefront enabling the engineering of point spread functions (PSFs) for single-molecule localization microscopy (SMLM) in three dimensions. As a model system for a non-transparent food colloid such as mayonnaise, we designed an oil-in-water emulsion containing the ferric ion binding protein phosvitin commonly present in egg yolk. We targeted phosvitin with fluorescently labelled primary antibodies and used PSF engineering to obtain two- and three-dimensional images of phosvitin covered oil droplets with sub 100 nm resolution. Our data indicated that phosvitin is homogeneously distributed at the interface. With the possibility to obtain super-resolved images in depth, our work paves the way for localizing biomacromolecules at heterogeneous colloidal interfaces in food emulsions. This article is part of the Theo Murphy meeting issue 'Super-resolution structured illumination microscopy (part 2)'.

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