Author: Joost Snijder; Andrew J. Borst; Annie Dosey; Alexandra C. Walls; Anika Burrell; Vijay S. Reddy; Justin M. Kollman; David Veesler
Title: Vitrification after multiple rounds of sample application and blotting improves particle density on cryo-electron microscopy grids Document date: 2016_12_15
ID: 2179jaes_1
Snippet: Single particle cryo-electron microscopy (cryoEM) is becoming an increasingly important tool in structural biology (Nogales and Scheres 2015; Cheng et al. 2015) . Due to recent advances in detector efficiency, microscope stability and image processing, the 3D structure of biomolecular complexes spanning a wide range of sizes, from haemoglobin to microtubules and intact viruses, can be reconstructed at (near-) atomic resolution (Bai et al. 2013; B.....
Document: Single particle cryo-electron microscopy (cryoEM) is becoming an increasingly important tool in structural biology (Nogales and Scheres 2015; Cheng et al. 2015) . Due to recent advances in detector efficiency, microscope stability and image processing, the 3D structure of biomolecular complexes spanning a wide range of sizes, from haemoglobin to microtubules and intact viruses, can be reconstructed at (near-) atomic resolution (Bai et al. 2013; Brilot et al. 2012; Campbell et al. 2012; Campbell et al. 2015; Koshouei et al. 2016; Liu et al. 2010; Nogales 2015; Scheres 2012; Walls et al. 2016a; Walls et al. 2016b) .
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