| Literature DB >> 33659324 |
Szilárd Szikora1,2, Tibor Novák2, Tamás Gajdos2, Miklós Erdélyi2, József Mihály1,2.
Abstract
Sarcomeres are extremely highly ordered macromolecular assemblies where proper structural organization is an absolute prerequisite to the functionality of these contractile units. Despite the wealth of information collected, the exact spatial arrangement of many of the H-zone and Z-disk proteins remained unknown. Recently, we developed a powerful nanoscopic approach to localize the sarcomeric protein components with a resolution well below the diffraction limit. The ease of sample preparation and the near crystalline structure of the Drosophila flight muscle sarcomeres make them ideally suitable for single molecule localization microscopy and structure averaging. Our approach allowed us to determine the position of dozens of H-zone and Z-disk proteins with a quasi-molecular, ~5-10 nm localization precision. The protocol described below provides an easy and reproducible method to prepare individual myofibrils for dSTORM imaging. In addition, it includes an in-depth description of a custom made and freely available software toolbox to process and quantitatively analyze the raw localization data.Entities:
Keywords: Drosophila flight muscles ; H-zone; IFM Analyzer; Quantitative localization microscopy; Sarcomere structure; Z-disk; dSTORM; rainSTORM
Year: 2020 PMID: 33659324 PMCID: PMC7842721 DOI: 10.21769/BioProtoc.3654
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325