Consequences of alkaline treatment for the ultrastructure of the acetylcholine-receptor-rich membranes from Torpedo marmorata electric organ.
Open Access
- 1 August 1981
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 90 (2) , 418-426
- https://doi.org/10.1083/jcb.90.2.418
Abstract
After fixation with glutaraldehyde and impregnation with tannic acid, the membrane that underlies the nerve terminals in T. marmorata electroplaque presents a typical asymmetric triple-layered structure with an unusual thickness. It is coated with electron-dense material on its inner, cytoplasmic face. Filamentous structures are frequently attached to these subsynaptic densities. The organization of the subsynaptic membrane is partly preserved after homogenization of the electric organ and purification of acetylcholine-receptor (AchR)-rich membrane fragments. In vitro treatment at pH 11 and 4.degree. C of these AchR-rich membranes releases an extrinsic protein of 43,000 MW and at the same time causes the complete disappearance of the cytoplasmic condensations. Freeze-etching of native membrane fragments discloses remnants of the ribbonlike organization of the AchR rosettes. This organization disappears after alkaline treatment and is replaced by a network which is not observed after rapid freezing and most likely results from the lateral redistribution of the AchR rosettes during condition of slow freezing. A dispersion of the AchR rosettes in the plane of the membrane also occurs after fusion of the pH 11-treated fragments with phospholipid vesicles. These results are interpreted in terms of a structural stabilization and immobilization of the AchR by the 43,000-Mr [molecular ratio] protein binding to the inner face of the subsynaptic membrane.This publication has 51 references indexed in Scilit:
- Distribution of macromolecules from the intercellular matrix in the electroplaque of Electrophorus electricusFEBS Letters, 1980
- Reconstitution of a Functional Acetylcholine ReceptorEuropean Journal of Biochemistry, 1980
- Transmembrane Orientation of Proteins Present in Acetylcholine Receptor‐Rich Membranes from Torpedo marmorata Studied by Selective ProteolysisEuropean Journal of Biochemistry, 1980
- Peptide extraction by alkaline treatment is accompanied by rearrangement of the membrane‐bound acetylcholine receptor from torpedo marmorataFEBS Letters, 1980
- Spectrin: Present status of a putative cyto-skeletal protein of the red cell membraneThe Journal of Membrane Biology, 1979
- Electrophorus acetylcholinesterase. Biochemical and electron microscope characterization of low ionic strength aggregatesThe Journal of cell biology, 1978
- Saturation transfer electron paramagnetic resonance on membrane bound proteins. II-absence of rotational diffusion of the cholinergic receptor protein in torpedo marmorata membrane fragmentsBiochemical and Biophysical Research Communications, 1977
- Synaptic membrane structure inTorpedo electric organJournal of Neurocytology, 1975
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- Use of uranyl formate as a negative stainJournal of Molecular Biology, 1965