Relevance of CARC and CRAC Cholesterol-Recognition Motifs in the nicotinic acetylcholine receptor and other membrane-bound receptors
Relevance of CARC and CRAC Cholesterol-Recognition Motifs in the nicotinic acetylcholine receptor and other membrane-bound receptors
Cholesterol is a ubiquitous neutral lipid, which finely tunes the activity of a wide range of membrane proteins, including neurotransmitter and hormone receptors and ion channels. Given the scarcity of available X-ray crystallographic structures and the even fewer in which cholesterol sites have been directly visualized, application of in silico computational methods remains a valid alternative for the detection and thermodynamic characterization of cholesterol-specific sites in functionally important membrane proteins. The membrane-embedded segments of the paradigm neurotransmitter receptor for acetylcholine display a series of cholesterol consensus domains (which we have coined “CARC”). The CARC motif exhibits a preference for the outer membrane leaflet and its mirror motif, CRAC, for the inner one. Some membrane proteins possess the double CARC–CRAC sequences within the same transmembrane domain. In addition to in silico molecular modeling, the affinity, concentration dependence, and specificity of the cholesterol-recognition motif–protein interaction have recently found experimental validation in other biophysical approaches like monolayer techniques and nuclear magnetic resonance spectroscopy. From the combined studies, it becomes apparent that the CARC motif is now more firmly established as a high-affinity cholesterol-binding domain for membrane-bound receptors and remarkably conserved along phylogenetic evolution.
Relevance of CARC and CRAC Cholesterol-Recognition Motifs in the Nicotinic Acetylcholine Receptor and Other Membrane-Bound Receptors. Available from: https://www.researchgate.net/publication/318333351_Relevance_of_CARC_and_CRAC_Cholesterol-Recognition_Motifs_in_the_Nicotinic_Acetylcholine_Receptor_and_Other_Membrane-Bound_Receptors [accessed Aug 1, 2017].
3-23
Di Scala, Corailie
8d457348-8165-47da-abf5-897d38b7076b
Baier, Carlos Javier
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Evans, Luke S.
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Williamson, Philip T.F.
0b7715c6-b60e-4e95-a1b1-6afc8b9f372a
Fantini, Jacques
dba30c1b-536b-460b-aaba-b7ef2d174c61
Barrantes, Francisco J.
e51a66c4-1f8f-429b-b1f4-9e8e191a33b6
2017
Di Scala, Corailie
8d457348-8165-47da-abf5-897d38b7076b
Baier, Carlos Javier
d1e8a69f-bfc3-4a9d-bda9-bb0b379230ff
Evans, Luke S.
c888a996-eb12-4e6b-9c2b-e6cda907674a
Williamson, Philip T.F.
0b7715c6-b60e-4e95-a1b1-6afc8b9f372a
Fantini, Jacques
dba30c1b-536b-460b-aaba-b7ef2d174c61
Barrantes, Francisco J.
e51a66c4-1f8f-429b-b1f4-9e8e191a33b6
Di Scala, Corailie, Baier, Carlos Javier, Evans, Luke S., Williamson, Philip T.F., Fantini, Jacques and Barrantes, Francisco J.
(2017)
Relevance of CARC and CRAC Cholesterol-Recognition Motifs in the nicotinic acetylcholine receptor and other membrane-bound receptors.
In,
Levitan, Irena
(ed.)
Current Topics in Membranes.
(Current Topics in Membranes, 80)
Elsevier, .
(doi:10.1016/bs.ctm.2017.05.001).
Record type:
Book Section
Abstract
Cholesterol is a ubiquitous neutral lipid, which finely tunes the activity of a wide range of membrane proteins, including neurotransmitter and hormone receptors and ion channels. Given the scarcity of available X-ray crystallographic structures and the even fewer in which cholesterol sites have been directly visualized, application of in silico computational methods remains a valid alternative for the detection and thermodynamic characterization of cholesterol-specific sites in functionally important membrane proteins. The membrane-embedded segments of the paradigm neurotransmitter receptor for acetylcholine display a series of cholesterol consensus domains (which we have coined “CARC”). The CARC motif exhibits a preference for the outer membrane leaflet and its mirror motif, CRAC, for the inner one. Some membrane proteins possess the double CARC–CRAC sequences within the same transmembrane domain. In addition to in silico molecular modeling, the affinity, concentration dependence, and specificity of the cholesterol-recognition motif–protein interaction have recently found experimental validation in other biophysical approaches like monolayer techniques and nuclear magnetic resonance spectroscopy. From the combined studies, it becomes apparent that the CARC motif is now more firmly established as a high-affinity cholesterol-binding domain for membrane-bound receptors and remarkably conserved along phylogenetic evolution.
Relevance of CARC and CRAC Cholesterol-Recognition Motifs in the Nicotinic Acetylcholine Receptor and Other Membrane-Bound Receptors. Available from: https://www.researchgate.net/publication/318333351_Relevance_of_CARC_and_CRAC_Cholesterol-Recognition_Motifs_in_the_Nicotinic_Acetylcholine_Receptor_and_Other_Membrane-Bound_Receptors [accessed Aug 1, 2017].
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e-pub ahead of print date: 10 July 2017
Published date: 2017
Identifiers
Local EPrints ID: 428886
URI: http://eprints.soton.ac.uk/id/eprint/428886
ISSN: 1063-5823
PURE UUID: dff38826-114f-42d3-a830-3d4570ce62ba
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Date deposited: 13 Mar 2019 19:19
Last modified: 16 Mar 2024 03:53
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Contributors
Author:
Corailie Di Scala
Author:
Carlos Javier Baier
Author:
Luke S. Evans
Author:
Jacques Fantini
Author:
Francisco J. Barrantes
Editor:
Irena Levitan
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