Imaging of Unstained DNA Origami Triangles with Electron Microscopy

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2019-08-13
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Londono‐Calderon, Alejandra
Hossen, Md Mir
Palo, Pierre
Bendickson, Lee
Vergara, Sandra
Nilsen-Hamilton, Marit
Hillier, Andrew
Prozorov, Tanya
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Nilsen-Hamilton, Marit
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Ames National LaboratoryChemical and Biological EngineeringBiochemistry, Biophysics and Molecular Biology, Roy J. Carver Department of
Abstract

Imaging of scaffolded DNA and DNA origami nanostructures has been dominated by atomic force microscopy of samples immobilized on bulk substrates. Less commonly used are electron microscopy techniques, typically carried out after negative staining of DNA structures or by using cryo‐transmission electron microscopy (TEM). Here, direct imaging of unstained DNA origami on common electron‐transparent substrates with utilizing high angular annular dark field scanning transmission electron microscopy (HAADF‐STEM) is reported. This approach establishes a method for depositing and imaging intact DNA triangles with mass‐thickness contrast sufficient to measure the scaffold‐to‐scaffold distances and the length of the triangle's seam. The signal‐to‐noise ratio (SNR) of the DNA supported on amorphous carbon as a function of the carbon thickness is measured on three types of commercially available TEM grids. This allows for edge detection of ≈1 nm height DNA triangles on carbon substrates as thick as ≈25 nm. Observations on the effect on SNR with the imaging modes are discussed. The effect of cation concentration used for pretreating the grid on the image resolution is also explored. This work presents proof‐of‐concept results demonstrating that electron microscopy can be used to resolve key elements of the DNA origami triangle without the use of staining protocols.

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