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Volume 271, Number 40,
Issue of October 4, 1996
pp. 24590-24597
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Structural Effects of Neutral and Anionic Lipids on the Nicotinic
Acetylcholine Receptor
AN INFRARED DIFFERENCE SPECTROSCOPY STUDY
(Received for publication, April 25, 1996, and in revised form, July 24, 1996)
Stephen E.
Ryan
,
Caroline N.
Demers
,
Jennifer P.
Chew
and
John E.
Baenziger
From the Department of Biochemistry, University of Ottawa, Ottawa,
Ontario K1H 8M5, Canada
The effects of both neutral and anionic lipids on
the structure of the nicotinic acetylcholine receptor (nAChR) have been
probed using infrared difference spectroscopy. The difference between
infrared spectra of the nAChR recorded using the attenuated total
reflectance technique in the presence and absence of the
neurotransmitter analog, carbamylcholine, exhibits a complex pattern of
positive and negative bands that provides a spectral map of the
structural changes that occur in the nAChR upon ligand binding and
subsequent desensitization. This spectral map is essentially identical
in difference spectra recorded from native, native alkaline-extracted,
and affinity-purified nAChR reconstituted into either soybean asolectin
or egg phosphatidylcholine membranes containing both neutral and
anionic lipids. This result suggests both a similar structure of the
nAChR and a similar resting to desensitized conformational change in
each membrane environment. In contrast, difference spectra recorded
from the nAChR reconstituted into egg phosphatidylcholine membranes
lacking neutral and/or anionic lipids all exhibit an essentially
identical pattern of band intensity variations, which is similar to the
pattern of variations observed in difference spectra recorded in the
continuous presence of the desensitizing local anesthetic, dibucaine.
The difference spectra suggest that the main effect of both neutral and
anionic lipids in a reconstituted egg phosphatidylcholine membrane is
to help stabilize the nAChR in a resting conformation. In the absence
of neutral and/or anionic lipids, the nAChR is converted into an
alternate conformation that appears to be analogous to the local
anesthetic-induced desensitized state. Significantly, the proportion of
receptors found in the resting versus the putative
desensitized state appears to be dependent upon the final lipid
composition of the reconstituted membrane. A
lipid-dependent modulation of the equilibrium between a
channel-active resting and channel-inactive desensitized state may
account for the modulations of nAChR activity that are observed in
different lipid membranes.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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