Annotation and automated segmentation of single-molecule localisation microscopy data.

IF 1.5 4区 工程技术 Q3 MICROSCOPY Journal of microscopy Pub Date : 2024-08-02 DOI:10.1111/jmi.13349
Oliver Umney, Joanna Leng, Gianluca Canettieri, Natalia A Riobo-Del Galdo, Hayley Slaney, Philip Quirke, Michelle Peckham, Alistair Curd
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Abstract

Single Molecule Localisation Microscopy (SMLM) is becoming a widely used technique in cell biology. After processing the images, the molecular localisations are typically stored in a table as xy (or xyz) coordinates, with additional information, such as number of photons, etc. This set of coordinates can be used to generate an image to visualise the molecular distribution, for example, a 2D or 3D histogram of localisations. Many different methods have been devised to analyse SMLM data, among which cluster analysis of the localisations is popular. However, it can be useful to first segment the data, to extract the localisations in a specific region of a cell or in individual cells, prior to downstream analysis. Here we describe a pipeline for annotating localisations in an SMLM dataset in which we compared membrane segmentation approaches, including Otsu thresholding and machine learning models, and subsequent cell segmentation. We used an SMLM dataset derived from dSTORM images of sectioned cell pellets, stained for the membrane proteins EGFR (epidermal growth factor receptor) and EREG (epiregulin) as a test dataset. We found that a Cellpose model retrained on our data performed the best in the membrane segmentation task, allowing us to perform downstream cluster analysis of membrane versus cell interior localisations. We anticipate this will be generally useful for SMLM analysis.

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单分子定位显微镜数据的注释和自动分割。
单分子定位显微镜(SMLM)正在成为细胞生物学中广泛使用的技术。处理图像后,分子定位通常以 xy(或 xyz)坐标的形式存储在表格中,并附带光子数等附加信息。这组坐标可用于生成可视化分子分布的图像,例如定位的二维或三维直方图。目前已设计出许多不同的方法来分析 SMLM 数据,其中定位的聚类分析比较流行。不过,在进行下游分析之前,首先对数据进行分割,提取细胞特定区域或单个细胞中的定位,可能会有所帮助。在这里,我们描述了在 SMLM 数据集中注释定位的流程,其中我们比较了膜分离方法(包括大津阈值化和机器学习模型)和后续的细胞分割。我们使用了一个 SMLM 数据集,该数据集来自对表皮生长因子受体和表皮生长因子蛋白进行染色的细胞颗粒切片 dSTORM 图像。我们发现,根据我们的数据重新训练的 Cellpose 模型在膜分离任务中表现最佳,使我们能够对膜与细胞内部定位进行下游聚类分析。我们预计这对 SMLM 分析普遍有用。
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来源期刊
Journal of microscopy
Journal of microscopy 工程技术-显微镜技术
CiteScore
4.30
自引率
5.00%
发文量
83
审稿时长
1 months
期刊介绍: The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit. The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens. Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.
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