介绍了一种灵活、稳健的单分子定位显微镜聚类分析方法Diinamic

Biological imaging Pub Date : 2023-07-10 eCollection Date: 2023-01-01 DOI:10.1017/S2633903X23000156
Anne-Lise Paupiah, Xavier Marques, Zaha Merlaud, Marion Russeau, Sabine Levi, Marianne Renner
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摘要

超分辨率显微镜使我们在纳米尺度上描述和解释生物组织的能力得到了重大改进。单分子定位显微镜(SMLM)使用分子的位置来创建超分辨率图像,但它也可以通过适当的点点分析来提供对分子组织的新见解,充分利用SMLM数据的稀疏特性。然而,SMLM的主要缺点是缺乏易于适用于生物样品中可能产生的各种类型数据的分析工具。通常,检测云可能是一簇分子,也可能不是,这取决于检测的局部密度,但也取决于分子本身的大小、标记技术、荧光团的光物理特性和成像条件。我们的目标是建立一个易于使用的聚类分析协议,以适应不同类型的数据。在这里,我们介绍diindynamic,它结合了不同的基于密度的分析和可选的阈值来促进聚类的检测。在模拟或真实的SMLM数据上,diindynamic可以正确识别不同大小和密度的簇,即使在每个荧光团有多个检测的嘈杂数据集中也能表现出色。它还在检测分布不均匀的簇中检测到子域(“纳米域”)。
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Introducing Diinamic, a flexible and robust method for clustering analysis in single-molecule localization microscopy.

Super-resolution microscopy allowed major improvements in our capacity to describe and explain biological organization at the nanoscale. Single-molecule localization microscopy (SMLM) uses the positions of molecules to create super-resolved images, but it can also provide new insights into the organization of molecules through appropriate pointillistic analyses that fully exploit the sparse nature of SMLM data. However, the main drawback of SMLM is the lack of analytical tools easily applicable to the diverse types of data that can arise from biological samples. Typically, a cloud of detections may be a cluster of molecules or not depending on the local density of detections, but also on the size of molecules themselves, the labeling technique, the photo-physics of the fluorophore, and the imaging conditions. We aimed to set an easy-to-use clustering analysis protocol adaptable to different types of data. Here, we introduce Diinamic, which combines different density-based analyses and optional thresholding to facilitate the detection of clusters. On simulated or real SMLM data, Diinamic correctly identified clusters of different sizes and densities, being performant even in noisy datasets with multiple detections per fluorophore. It also detected subdomains ("nanodomains") in clusters with non-homogeneous distribution of detections.

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