Role of surfactants in electron cryo-microscopy film preparation

被引:6
作者
Michon, Baptiste [1 ,2 ]
Lopez-Sanchez, Uriel [3 ]
Degrouard, Jeril [4 ]
Nury, Hugues [3 ]
Leforestier, Amelie [4 ]
Rio, Emmanuelle [4 ]
Salonen, Anniina [4 ]
Zoonens, Manuela [1 ,2 ]
机构
[1] Univ Paris Cite, Lab Biol Phys Chim Proteines Membranaires, CNRS, UMR 7099, Paris, France
[2] Fdn Edmond Rothschild Dev Rech Sci, Inst Biol Phys Chim, Paris, France
[3] Inst Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France
[4] Univ Paris Saclay, CNRS, Lab Phys Solides, Orsay, France
关键词
CRYOELECTRON MICROSCOPY; MEMBRANE-PROTEINS; AMPHIPATHIC POLYMERS; HYDROPHOBIC GROUPS; CRYO-EM; SINGLE; SOLUBILIZATION; AMPHIPOLS; STABILIZATION; AMPHIPHILES;
D O I
10.1016/j.bpj.2023.04.016
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Single-particle electron cryo-microscopy (cryo-EM) has become an effective and straightforward approach to determine the structure of membrane proteins. However, obtaining cryo-EM grids of sufficient quality for high-resolution structural analysis remains a major bottleneck. One of the difficulties arises from the presence of detergents, which often leads to a lack of control of the ice thickness. Amphipathic polymers such as amphipols (APols) are detergent substitutes, which have proven to be valuable tools for cryo-EM studies. In this work, we investigate the physico-chemical behavior of APol-and detergent-containing solutions and show a correlation with the properties of vitreous thin films in cryo-EM grids. This study provides new insight on the potential of APols, allowing a better control of ice thickness while limiting protein adsorption at the air-water interface, as shown with the full-length mouse serotonin 5-HT3A receptor whose structure has been solved in APol. These findings may speed up the process of grid optimization to obtain high-resolution structures of membrane proteins.
引用
收藏
页码:1846 / 1857
页数:12
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