| Literature DB >> 23531637 |
Elizabeth A Smith1, Bertrand P Cinquin, Gerry McDermott, Mark A Le Gros, Dilworth Y Parkinson, Hong Tae Kim, Carolyn A Larabell.
Abstract
Correlative microscopy techniques interrogate biological systems more thoroughly than is possible using a single modality. This is particularly true if disparate data types can be acquired from the same specimen. Recently, there has been significant progress towards combining the structural information obtained from soft X-ray tomography (SXT) with molecular localization data. Here we will compare methods for determining the position of molecules in a cell viewed by SXT, including direct visualization using electron dense labels, and by indirect methods, such as fluorescence microscopy and high numerical aperture cryo-light microscopy. We will also discuss available options for preserving the in vivo structure and organization of the specimen during multi-modal data collection, and how some simple specimen mounting concepts can ensure maximal data completeness in correlative imaging experiments.Entities:
Keywords: CFM; Cellular imaging; Cryo-Flourescence microscopy; FM; Hybrid methods; LAC; Localization; PSF; SXT; Tomography; YFP; cryogenic fluorescence microscopy; fluorescence microscopy; linear absorption coefficient; point spread function; soft X-ray tomography; yellow fluorescent protein
Mesh:
Year: 2013 PMID: 23531637 PMCID: PMC3758393 DOI: 10.1016/j.jsb.2013.03.006
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867