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- Title
Incorporation Of Membrane Proteins Into Lipid Bilayers For Scanning Transmission Electron Microscopy And Single Particle Reconstruction.
- Authors
Bailey, GW; Jerome, WG; McKernan, S; Mansfield, JF; Price, RL; McAlduff, DE; Heng, YM; Ottensmeyer, FP
- Abstract
The experimental approaches available to study the structure of most membrane proteins are limited. X-ray crystallography or electron crystallography rely on the availability or creation of 3D or 2D crystals to obtain high resolution structural information of membrane proteins. Single particleimaging of detergent solubilized protein is also possible, but removes the protein from its native environment. Torecreate suchan environment, we have developed a method which permits membrane proteins to be visualized in a lipid bilayer support. A copper grid overlaid with a holey plastic film is vertically submerged into a lipid monolayer (Fig.l). This action creates planar lipid bilayers spanning 1 to 10 μm holes of the plastic film. These synthetic membranes have a thickness of approximately 40 Å, comparable to literature values for various cell membranes and are reasonably stable under a defocused beam in a transmission electron microscope (TEM)(Fig.2). Proteoliposomes with appropriate proteins in their membrane are added to the still-wet fresh lipid bilayers such that the liposomes fuse with the planar membrane (Fig.3).
- Publication
Microscopy & Microanalysis, 1999, p1314
- ISSN
1431-9276
- Publication type
Article
- DOI
10.1017/S1431927600019899