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使用电可调透镜实现超分辨率显微镜的实时三维稳定。

Real-time 3D stabilization of a super-resolution microscope using an electrically tunable lens.

作者信息

Tafteh Reza, Abraham Libin, Seo Denny, Lu Henry Y, Gold Michael R, Chou Keng C

出版信息

Opt Express. 2016 Oct 3;24(20):22959-22970. doi: 10.1364/OE.24.022959.

Abstract

Single-molecule localization microscopy (SMLM) has become an essential tool for examining a wide variety of biological structures and processes. However, the relatively long acquisition time makes SMLM prone to drift-induced artifacts. Here we report an optical design with an electrically tunable lens (ETL) that actively stabilizes a SMLM in three dimensions and nearly eliminates the mechanical drift (RMS ~0.7 nm lateral and ~2.7 nm axial). The bifocal design that employed fiducial markers on the coverslip was able to stabilize the sample regardless of the imaging depth. The effectiveness of the ETL was demonstrated by imaging endosomal transferrin receptors near the apical surface of B-lymphocytes at a depth of 8 µm. The drift-free images obtained with the stabilization system showed that the transferrin receptors were present in distinct but heterogeneous clusters with a bimodal size distribution. In contrast, the images obtained without the stabilization system showed a broader unimodal size distribution. Thus, this stabilization system enables a more accurate analysis of cluster topology. Additionally, this ETL-based stabilization system is cost-effective and can be integrated into existing microscopy systems.

摘要

单分子定位显微镜(SMLM)已成为研究各种生物结构和过程的重要工具。然而,相对较长的采集时间使SMLM容易出现漂移诱导的伪影。在此,我们报告一种采用电可调透镜(ETL)的光学设计,该设计可在三个维度上主动稳定SMLM,并几乎消除机械漂移(横向均方根误差约为0.7 nm,轴向约为2.7 nm)。在盖玻片上使用基准标记的双焦点设计能够稳定样品,而与成像深度无关。通过对B淋巴细胞顶端表面下方8 µm深处的内体转铁蛋白受体进行成像,证明了ETL的有效性。使用稳定系统获得的无漂移图像显示,转铁蛋白受体存在于不同但异质的簇中,具有双峰大小分布。相比之下,没有稳定系统获得的图像显示出更宽的单峰大小分布。因此,该稳定系统能够更准确地分析簇拓扑结构。此外,这种基于ETL的稳定系统具有成本效益,并且可以集成到现有的显微镜系统中。

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