Abstract

Difficulties associated with using X-ray crystallography for structural studies of large macromolecular complexes have made single particle cryo-electron microscopy (cryoEM) a key technique in structural biology. The efficient application of the single particle cryoEM approach requires the sample to be vitrified within the holes of carbon films, with particles well dispersed throughout the ice and adopting multiple orientations. To achieve this, the carbon support film is first hydrophilised by glow discharge, which allows the sample to spread over the film. Unfortunately, for transmembrane complexes especially, this procedure can result in severe sample adsorption to the carbon support film, reducing the number of particles dispersed in the ice. This problem is rate-limiting in the single particle cryoEM approach and has hindered its widespread application to hydrophobic complexes. We describe a novel grid preparation technique that allows for good particle dispersion in the ice and minimal hydrophobic particle adhesion to the support film. This is achieved by hydrophilisation of the carbon support film by the use of selected detergents that interact with the support so as to achieve a hydrophilic and neutral or selectively charged surface.

Highlights

  • The popularity of cryo-electron microscopy (cryoEM) for structural analysis of macromolecular assemblies is due to the speed and ease of the data collection procedure

  • Single particle cryoEM involves the suspension of macromolecules in vitrified ice, acquisition of data at low temperature and low electron dose and computerised processing of the images

  • The key difference between holey and continuous carbon supports is the role of the carbon

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Summary

Introduction

The popularity of cryoEM for structural analysis of macromolecular assemblies is due to the speed and ease of the data collection procedure. Single particle cryoEM involves the suspension of macromolecules in vitrified ice, acquisition of data at low temperature and low electron dose and computerised processing of the images. This technique retains the complexes in a hydrated state, giving a good representation of their native structure. Continuous carbon support films are often used because particles do not distribute efficiently into the holes. This improves particle spread but limits the observable particle orientations. The carbon makes the image contrast of the particles lower, impairing high-accuracy alignment required for extraction of high-resolution image information

Consequences of grid preparation by glow discharge
Transmembrane macromolecular complexes and cryoEM
Grid types used
Detergent selection and concentration
Grid pretreatment procedure
Samples tested
Microscopy conditions
10. DDM pretreatment decreases membrane protein binding to the carbon surface
14. Conclusions

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