开源3D荧光显微镜活性样品稳定。

IF 2.4 Q3 BIOPHYSICS
Sanket Patil, Giuseppe Vicidomini, Eli Slenders
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引用次数: 0

摘要

超分辨率显微镜使纳米级分辨率成像成为可能。然而,要在不引入可能误导数据解释的伪影的情况下获得这种级别的细节,需要在整个成像采集过程中保持样品的稳定性。这个过程可以从几秒钟到几个小时不等,特别是当活细胞成像与超分辨率技术相结合时。在这里,我们提出了一个基于实时跟踪基准标记的三维主动样品稳定系统。为了确保广泛的可及性,系统采用现成的光学和光子元件设计。此外,附带的软件是开源的,用Python编写,便于社区采用和定制。我们实现了样品在1纳米内的横向和轴向移动的标准偏差,持续时间在小时范围内。我们的方法可以很容易地集成到现有的显微镜中,不仅使长时间的超分辨率显微镜更容易获得,而且还允许共聚焦和宽视场活细胞成像实验跨越数小时甚至数天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Open-source 3D active sample stabilization for fluorescence microscopy.

Super-resolution microscopy has enabled imaging at nanometer-scale resolution. However, achieving this level of detail without introducing artifacts that could mislead data interpretation requires maintaining sample stability throughout the entire imaging acquisition. This process can range from a few seconds to several hours, particularly when combining live-cell imaging with super-resolution techniques. Here, we present a three-dimensional active sample stabilization system based on real-time tracking of fiducial markers. To ensure broad accessibility, the system is designed using readily available off-the-shelf optical and photonic components. Additionally, the accompanying software is open source and written in Python, facilitating adoption and customization by the community. We achieve a standard deviation of the sample movement within 1 nm in both the lateral and axial directions for a duration in the range of hours. Our approach allows easy integration into existing microscopes, not only making prolonged super-resolution microscopy more accessible but also allowing confocal and widefield live-cell imaging experiments spanning hours or even days.

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来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
自引率
0.00%
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0
审稿时长
75 days
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