Imaging and structural studies of DNA–protein complexes and membrane ion channels
Author(s) -
Monica Marini,
Tania Limongi,
Andrea Falqui,
Alessandro Genovese,
Marco Allione,
Manola Moretti,
Sergei Lopatin,
Luca Tirinato,
Gobind Das,
Bruno Torre,
Andrea Giugni,
Fabrizia Cesca,
Fabio Benfenati,
Enzo Di Fabrizio
Publication year - 2017
Publication title -
nanoscale
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.038
H-Index - 224
eISSN - 2040-3372
pISSN - 2040-3364
DOI - 10.1039/c6nr07958j
Subject(s) - ion channel , dna , biophysics , membrane , membrane protein , ion , chemistry , materials science , computational biology , nanotechnology , biochemistry , biology , receptor , organic chemistry
In bio-imaging by electron microscopy, damage of the sample and limited contrast are the two main hurdles for reaching high image quality. We extend a new preparation method based on nanofabrication and super-hydrophobicity to the imaging and structural studies of nucleic acids, nucleic acid-protein complexes (DNA/Rad51 repair protein complex) and neuronal ion channels (gap-junction, K + and GABA A channels) as paradigms of biological significance and increasing complexity. The preparation method is based on the liquid phase and is compatible with physiological conditions. Only in the very last stage, samples are dried for TEM analysis. Conventional TEM and high-resolution TEM (HRTEM) were used to achieve a resolution of 3.3 and 1.5 Å, respectively. The EM dataset quality allows the determination of relevant structural and metrological information on the DNA structure, DNA-protein interactions and ion channels, allowing the identification of specific macromolecules and their structure.
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