Cryo-Electron Microscopy (EM) is a powerful technique to visualize biological processes at nanometer resolution. Structural studies of macromolecular assemblies are typically performed on individual complexes that are biochemically isolated from their cellular context. Here we present a molecular imaging platform to capture and view multiple components of cellular pathways within a functionally relevant framework. We utilized the bacterial protein synthesis machinery as a model system to develop our approach. By using modified Affinity Grid surfaces, we were able to recruit multiple protein assemblies bound to nascent strands of mRNA. The combined use of Affinity Capture technology and single particle electron microscopy provide the basis for visualizing RNA-dependent pathways in a remarkable new way.
Capturing RNA-dependent pathways for cryo-EM analysis
Justin R. Tanner,Katherine E. Degen,Brian L. Gilmore,Deborah F. Kelly
Published 2012 in Computational and Structural Biotechnology Journal
ABSTRACT
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- Publication year
2012
- Venue
Computational and Structural Biotechnology Journal
- Publication date
2012-02-23
- Fields of study
Biology, Medicine, Materials Science, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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