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使用 NoiSee 工作流程来测量共聚焦显微镜的信噪比值。

Using the NoiSee workflow to measure signal-to-noise ratios of confocal microscopes.

机构信息

Imaging Core Facility, Biozentrum, University of Basel, Klingelbergstrasse 50-70, 4056, Basel, Switzerland.

出版信息

Sci Rep. 2019 Feb 4;9(1):1165. doi: 10.1038/s41598-018-37781-3.

Abstract

Confocal microscopy is used today on a daily basis in life science labs. This "routine" technique contributes to the progress of scientific projects across many fields by revealing structural details and molecular localization, but researchers need to be aware that detection efficiency and emission light path performance is of major influence in the confocal image quality. By design, a large portion of the signal is discarded in confocal imaging, leading to a decreased signal-to-noise ratio (SNR) which in turn limits resolution. A well-aligned system and high performance detectors are needed in order to generate an image of best quality. However, a convenient method to address system status and performance on the emission side is still lacking. Here, we present a complete method to assess microscope and emission light path performance in terms of SNR, with a comprehensive protocol alongside NoiSee, an easy-to-use macro for Fiji (available via the corresponding update site). We used this method to compare several confocal systems in our facility on biological samples under typical imaging conditions. Our method reveals differences in microscope performance and highlights the various detector types used (multialkali photomultiplier tube (PMT), gallium arsenide phosphide (GaAsP) PMT, and Hybrid detector). Altogether, our method will provide useful information to research groups and facilities to diagnose their confocal microscopes.

摘要

共聚焦显微镜如今在生命科学实验室中得到了广泛应用。这项“常规”技术通过揭示结构细节和分子定位,推动了许多领域的科学项目的进展,但研究人员需要意识到,检测效率和发射光路性能对共焦图像质量有重大影响。设计上,共聚焦成像会丢弃大量信号,导致信噪比(SNR)降低,从而限制分辨率。为了生成最佳质量的图像,需要一个良好对齐的系统和高性能的探测器。然而,在发射端仍然缺乏一种方便的方法来解决系统状态和性能的问题。在这里,我们提出了一种完整的方法来评估显微镜和发射光路的 SNR 性能,同时还提供了一个与 NoiSee 配套的综合协议,这是一个易于在 Fiji 中使用的宏(可通过相应的更新站点获得)。我们使用这种方法在我们的实验室中对几种共聚焦系统进行了比较,这些系统在典型的成像条件下对生物样本进行了成像。我们的方法揭示了显微镜性能的差异,并强调了使用的各种探测器类型(多碱光电倍增管(PMT)、砷化镓磷(GaAsP)PMT 和混合探测器)。总之,我们的方法将为研究小组和实验室提供有用的信息,以诊断他们的共焦显微镜。

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