| Literature DB >> 35218547 |
Abstract
The structural organization of macromolecules and their association in assemblies and organelles is key to understand cellular function. Super-resolution fluorescence microscopy has expanded our toolbox for examining such nanometer-scale cellular structures, by enabling positional mapping of proteins in situ. Here, we detail the workflow to build nanometer-scale maps focusing on two complementary super-resolution modalities: structured illumination microscopy (SIM) and stochastic optical reconstruction microscopy (STORM).Entities:
Keywords: Centrosome; Cilia; Macromolecular assembly organization; SIM; STORM; Subdiffraction imaging; Super-resolution fluorescence microscopy
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Year: 2022 PMID: 35218547 DOI: 10.1007/978-1-0716-2051-9_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745