Atomic force microscopy of cloned nicotinic acetylcholine receptor expressed in Xenopus oocytes.
Author(s) -
Ratnesh Lal,
Liang Yu
Publication year - 1993
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.90.15.7280
Subject(s) - acetylcholine receptor , xenopus , torpedo , biophysics , nicotinic agonist , nicotinic acetylcholine receptor , acetylcholine , neuromuscular junction , membrane , receptor , chemistry , extracellular , microbiology and biotechnology , biology , biochemistry , endocrinology , gene , neuroscience
The nicotinic acetylcholine receptor (AChR) was expressed in Xenopus oocytes from in vitro transcribed mRNA and was imaged by atomic force microscopy. A characteristic pentameric structure of AChR was readily observed on the extracellular face of the cell membrane, with a central pore surrounded by protruding AChR subunits. These structures were seen only in mRNA-injected oocytes that also gave acetylcholine-induced membrane currents. The size of individual AChR channels, the angles between subunits, and the interchannel spacing were all compatible with the current model of AChR. In addition, localized patches of microscopic AChR clustering were observed, with packing density approaching that at the neuromuscular junction. These findings show the potential of studying cloned membrane proteins in oocytes for both their surface topography and their structure-function relationship in native membrane without the need for crystallization.
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