Demonstrates the use of metal-tagging transmission electron microscopy to visualize the 3D organization of viral replicase complexes in cells, providing a method to study protein activation and identify antiviral targets.
Advances imaging of viral replicase organization in cells; leaves open translation to antiviral target identification.
Positive-strand RNA viruses, which can be devastating pathogens in humans, animals and plants, replicate their genomes on intracellular membranes. Here, we describe the three-dimensional ultrastructural organization of a tombusvirus replicase in yeast, a valuable model for exploring virus-host interactions. We visualized the intracellular distribution of a viral replicase protein using metal-tagging transmission electron microscopy, a highly sensitive nanotechnology whose full potential remains to be developed. These three-dimensional images show how viral replicase molecules are organized when they are incorporated into the active domains of the intracellular replication compartment. Our approach provides a means to study protein activation mechanisms in cells and to identify targets for new antiviral compounds.
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Castro et al. (2016) studied this question.
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