Chromatin Biology & Epigenetics Lab, Department of Cellular, Computational, and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
Laboratoire Angevin de Recherche en Ingénierie des Systèmes, UMR INRAE IRHS, Université d'Angers, Angers, France.
Methods Mol Biol. 2023;2655:183-200. doi: 10.1007/978-1-0716-3143-0_14.
The polycomb group (PcG) proteins play a central role in the maintenance of a repressive state of gene expression. Recent findings demonstrate that PcG components are organized into nuclear condensates, contributing to the reshaping of chromatin architecture in physiological and pathological conditions, thus affecting the nuclear mechanics. In this context, direct stochastic optical reconstruction microscopy (dSTORM) provides an effective tool to achieve a detailed characterization of PcG condensates by visualizing them at a nanometric level. Furthermore, by analyzing dSTORM datasets with cluster analysis algorithms, quantitative information can be yielded regarding protein numbers, grouping, and spatial organization. Here, we describe how to set up a dSTORM experiment and perform the data analysis to study PcG complexes' components in adhesion cells quantitatively.
多梳抑制复合物(PcG)蛋白在维持基因表达的抑制状态中起着核心作用。最近的研究结果表明,PcG 成分被组织成核凝聚体,有助于在生理和病理条件下重塑染色质结构,从而影响核力学。在这种情况下,直接随机光学重建显微镜(dSTORM)通过在纳米级水平上对 PcG 凝聚体进行可视化,提供了一种有效的工具来实现对它们的详细表征。此外,通过使用聚类分析算法分析 dSTORM 数据集,可以获得关于蛋白质数量、分组和空间组织的定量信息。在这里,我们描述了如何设置 dSTORM 实验并进行数据分析,以定量研究黏附细胞中 PcG 复合物的组成。