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The application of support layers to cryogenic electron microscopy (cryoEM) grids can increase particle density, limit interactions with the air-water interface, reduce beam-induced motion, and improve the distribution of particle orientations. This paper describes a robust protocol for coating cryoEM grids with a monolayer of graphene for improved cryo-sample preparation.
In cryogenic electron microscopy (cryoEM), purified macromolecules are applied to a grid bearing a holey carbon foil; the molecules are then blotted to remove excess liquid and rapidly frozen in a roughly 20-100 nm thick layer of vitreous ice, suspended across roughly 1 µm wide foil holes. The resulting sample is imaged using cryogenic transmission electron microscopy, and after image processing using suitable software, near-atomic resolution structures can be determined. Despite cryoEM's widespread adoption, sample preparation remains a severe bottleneck in cryoEM workflows, with users often encountering challenges related to samples behaving poorly in the suspended vitreous ice. Recently, methods have been developed to modify cryoEM grids with a single continuous layer of graphene, which acts as a support surface that often increases particle density in the imaged area and can reduce interactions between particles and the air-water interface. Here, we provide detailed protocols for the application of graphene to cryoEM grids and for rapidly assessing the relative hydrophilicity of the resulting grids. Additionally, we describe an EM-based method to confirm the presence of graphene by visualizing its characteristic diffraction pattern. Finally, we demonstrate the utility of these graphene supports by rapidly reconstructing a 2.7 Å resolution density map of a Cas9 complex using a pure sample at a relatively low concentration.
Single particle cryogenic electron microscopy (cryoEM) has evolved into a widely used method for visualizing biological macromolecules1. Fueled by advances in direct electron detection2,3,4, data acquisition5, and image processing algorithms6,7,8,9,10, cryoEM is now capable of producing near-atomic resolution 3D structures of a fast-growing number of macromolecules
1. Preparation of CVD graphene
Successful fabrication of graphene-coated cryoEM grids using the equipment (Figure 1) and protocol (Figure 2) outlined here will result in a monolayer of graphene covering the foil holes that can be confirmed by its characteristic diffraction pattern. To promote protein adsorption to the graphene surface, UV/ozone treatment can be used to render the surface hydrophilic by installing oxygen-containing functional groups. However, hydrocarbon contaminants in the ai.......
CryoEM sample preparation involves a host of technical challenges, with most workflows requiring researchers to manually manipulate fragile grids with extreme care to avoid damaging them. Additionally, the amenability of any sample to vitrification is unpredictable; particles often interact with the air-water-interface or with the solid support foil overlaying the grids, which can lead to particles adopting preferred orientations or failing to enter the imaging holes unless very high protein concentrations are applied
Specimens were prepared and imaged at the CryoEM Facility in MIT.nano on microscopes acquired thanks to the Arnold and Mabel Beckman Foundation. Contact angle imaging devices were printed at the MIT Metropolis Maker Space. We thank the laboratories of Nieng Yan and Yimo Han, and staff at MIT.nano for their support throughout the adoption of this method. In particular, we extend our thanks to Drs. Guanhui Gao and Sarah Sterling for their insightful discussions and feedback. This work was supported by NIH grants R01-GM144542, 5T32-GM007287, and NSF-CAREER grant 2046778. Research in the Davis lab is supported by the Alfred P. Sloan Foundation, the James H. Ferry Fund, th....
Name | Company | Catalog Number | Comments |
250 mL beaker (3x) | Fisher | 02-555-25B | |
50 mL beaker (2x) | Corning | 1000-50 | |
Acetone | Fisher | A949-4 | |
Aluminum foil | Fisher | 15-078-292 | |
Ammonium persulfate | Fisher | (I17874 | |
Coverslips 50 mm x 24 mm | Mattek | PCS-1.5-5024 | |
CVD graphene | Graphene Supermarket | CVD-Cu-2x2 | |
easiGlow discharger | Ted-Pella | 91000S | |
Ethanol | Millipore-Sigma | 1.11727 | |
Flat-tip tweezers | Fisher | 50-239-60 | |
Glass cutter | Grainger | 21UE26 | |
Glass petri plate and cover | VWR | 75845-544 | |
Glass serological pipette | Fisher | 13-676-34D | |
Grid Storage Case | EMS | 71146-02 | |
Hot plate | Fisher | 07-770-108 | |
Isopropanol | Sigma | W292907 | |
Kimwipe | Fisher | 06-666 | |
Lab scissors | Fisher | 13-806-2 | |
Methyl-Methacrylate EL-6 | Kayaku | MMA M310006 0500L1GL | |
Molecular grade water | Corning | 46-000-CM | |
Negative action tweezers (2x) | Fisher | 50-242-78 | |
P20 pipette | Rainin | 17014392 | |
P200 pipette | Rainin | 17008652 | |
Parafilm | Fisher | 13-374-12 | |
Pipette tips | Rainin | 30389291 | |
Quantifoil grids with holey carbon | EMS | Q2100CR1 | |
Spin coater | SetCas | KW-4A | with chuck SCA-19-23 |
Straightedge | ULINE | H-6560 | |
Thermometer | Grainger | 3LRD1 | |
UV/Ozone cleaner | BioForce | SKU: PC440 | |
Vacuum desiccator | Thomas Scientific | 1159X11 | |
Whatman paper | VWR | 28297-216 |
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