| Literature DB >> 26436577 |
Matthias Schürmann1, Natalie Frese2, André Beyer2, Peter Heimann1, Darius Widera1,3, Viola Mönkemöller2, Thomas Huser2, Barbara Kaltschmidt1, Christian Kaltschmidt1, Armin Gölzhäuser2.
Abstract
Cell membranes are composed of 2D bilayers of amphipathic lipids, which allow a lateral movement of the respective membrane components. These components are arranged in an inhomogeneous manner as transient micro- and nanodomains, which are believed to be crucially involved in the regulation of signal transduction pathways in mammalian cells. Because of their small size (diameter 10-200 nm), membrane nanodomains cannot be directly imaged using conventional light microscopy. Here, direct visualization of cell membrane nanodomains by helium ion microscopy (HIM) is presented. It is shown that HIM is capable to image biological specimens without any conductive coating and that HIM images clearly allow the identification of nanodomains in the ultrastructure of membranes with 1.5 nm resolution. The shape of these nanodomains is preserved by fixation of the surrounding unsaturated fatty acids while saturated fatty acids inside the nanodomains are selectively removed. Atomic force microscopy, fluorescence microscopy, 3D structured illumination microscopy, and direct stochastic optical reconstruction microscopy provide additional evidence that the structures in the HIM images of cell membranes originate from membrane nanodomains. The nanodomains observed by HIM have an average diameter of 20 nm and are densely arranged with a minimal nearest neighbor distance of ≈ 15 nm.Entities:
Keywords: atomic force microscopy; bioimaging; helium ion microscopy; lipid nanodomains; lipid rafts
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Year: 2015 PMID: 26436577 DOI: 10.1002/smll.201501540
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281