Dual-Affinity Graphene Sheets for High-Resolution Cryo-Electron Microscopy .
Hang ChengLiming ZhengNan LiuCongyuan HuangJie XuYe LuXiaoya CuiKui XuYuan HouJunchuan TangZhong ZhangJing LiXiaodan NiYanan ChenHai-Lin PengHong-Wei WangPublished in: Journal of the American Chemical Society (2023)
With the development of cryo-electron microscopy (cryo-EM), high-resolution structures of macromolecules can be reconstructed by the single particle method efficiently. However, challenges may still persist during the specimen preparation stage. Specifically, proteins tend to adsorb at the air-water interface and exhibit a preferred orientation in vitreous ice. To overcome these challenges, we have explored dual-affinity graphene (DAG) modified with two different affinity ligands as a supporting material for cryo-EM sample preparation. The ligands can bind to distinct sites on the corresponding tagged particles, which in turn generates various orientation distributions of particles and prevents the adsorption of protein particles onto the air-water interface. As expected, the DAG exhibited high binding specificity and affinity to target macromolecules, resulting in more balanced particle Euler angular distributions compared to single functionalized graphene on two different protein cases, including the SARS -CoV-2 spike glycoprotein. We anticipate that the DAG grids will enable facile and efficient three-dimensional (3D) reconstruction for cryo-EM structural determination, providing a robust and general technique for future studies.
Keyphrases
- electron microscopy
- high resolution
- molecularly imprinted
- sars cov
- capillary electrophoresis
- mass spectrometry
- room temperature
- binding protein
- quantum dots
- carbon nanotubes
- protein protein
- mouse model
- living cells
- current status
- sensitive detection
- coronavirus disease
- tandem mass spectrometry
- monte carlo
- liquid chromatography