| Literature DB >> 33606980 |
Emma Silvester1, Benjamin Vollmer2, Vojtěch Pražák2, Daven Vasishtan2, Emily A Machala3, Catheryne Whittle3, Susan Black2, Jonathan Bath4, Andrew J Turberfield5, Kay Grünewald6, Lindsay A Baker7.
Abstract
Electron cryotomography (cryoET), an electron cryomicroscopy (cryoEM) modality, has changed our understanding of biological function by revealing the native molecular details of membranes, viruses, and cells. However, identification of individual molecules within tomograms from cryoET is challenging because of sample crowding and low signal-to-noise ratios. Here, we present a tagging strategy for cryoET that precisely identifies individual protein complexes in tomograms without relying on metal clusters. Our method makes use of DNA origami to produce "molecular signposts" that target molecules of interest, here via fluorescent fusion proteins, providing a platform generally applicable to biological surfaces. We demonstrate the specificity of signpost origami tags (SPOTs) in vitro as well as their suitability for cryoET of membrane vesicles, enveloped viruses, and the exterior of intact mammalian cells.Entities:
Keywords: DNA origami; aptamers; cellular electron cryotomography; cryoEM; electron cryomicroscopy; labeling; molecular arrows; protein localisation; signpost origami tags; tagging
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Year: 2021 PMID: 33606980 PMCID: PMC7895908 DOI: 10.1016/j.cell.2021.01.033
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582