Literature DB >> 23500069

Superb resolution and contrast of transmission electron microscopy images of unstained biological samples on graphene-coated grids.

Jaekyun Jeon1, Michael S Lodge, Ben D Dawson, Masa Ishigami, Frank Shewmaker, Bo Chen.   

Abstract

BACKGROUND: In standard transmission electron microscopy (TEM), biological samples are supported on carbon films of nanometer thickness. Due to the similar electron scattering of protein samples and graphite supports, high quality images with structural details are obtained primarily by staining with heavy metals.
METHODS: Single-layered graphene is used to support the protein self-assemblies of different molecular weights for qualitative and quantitative characterizations.
RESULTS: We show unprecedented high resolution and contrast images of unstained samples on graphene on a low-end TEM. We show for the first time that the resolution and contrast of TEM images of unstained biological samples with high packing density in their native states supported on graphene can be comparable or superior to uranyl acetate-stained TEM images.
CONCLUSION: Our results demonstrate a novel technique for TEM structural characterization to circumvent the potential artifacts caused by staining agents without sacrificing image resolution or contrast, and eliminate the need for toxic metals. Moreover, this technique better preserves sample integrity for quantitative characterization by dark-field imaging with reduced beam damage. GENERAL SIGNIFICANCE: This technique can be an effective alternative for bright-field qualitative characterization of biological samples with high packing density and those not amenable to the standard negative staining technique, in addition to providing high quality dark-field unstained images at reduced radiation damage to determine quantitative structural information of biological samples. Published by Elsevier B.V.

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Year:  2013        PMID: 23500069     DOI: 10.1016/j.bbagen.2013.03.002

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  1 in total

1.  MED15 prion-like domain forms a coiled-coil responsible for its amyloid conversion and propagation.

Authors:  Cristina Batlle; Isabel Calvo; Valentin Iglesias; Cian J Lynch; Marcos Gil-Garcia; Manuel Serrano; Salvador Ventura
Journal:  Commun Biol       Date:  2021-03-26
  1 in total

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