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Assessment of homology templates and an anesthetic binding site within the ?-aminobutyric acid receptor

Bertaccini, E. J. (author)
Yoluk, Özge (author)
KTH,Beräkningsbiofysik,Science for Life Laboratory, SciLifeLab
Lindahl, Erik R. (author)
KTH,Beräkningsbiofysik,Science for Life Laboratory, SciLifeLab
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Trudell, James Robert (author)
Department of Anesthesia, Stanford University School of Medicine, United States
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 (creator_code:org_t)
2013
2013
English.
In: Anesthesiology. - 0003-3022 .- 1528-1175. ; 119:5, s. 1087-1095
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Anesthetics mediate portions of their activity via modulation of the ?-aminobutyric acid receptor (GABAaR). Although its molecular structure remains unknown, significant progress has been made toward understanding its interactions with anesthetics via molecular modeling. Methods: The structure of the torpedo acetylcholine receptor (nAChR?), the structures of the ?4 and ?2 subunits of the human nAChR, the structures of the eukaryotic glutamate-gated chloride channel (GluCl), and the prokaryotic pH-sensing channels, from Gloeobacter violaceus and Erwinia chrysanthemi, were aligned with the SAlign and 3DMA algorithms. A multiple sequence alignment from these structures and those of the GABAaR was performed with ClustalW. The Modeler and Rosetta algorithms independently created three-dimensional constructs of the GABAaR from the GluCl template. The CDocker algorithm docked a congeneric series of propofol derivatives into the binding pocket and scored calculated binding affinities for correlation with known GABAaR potentiation EC50s. Results: Multiple structure alignments of templates revealed a clear consensus of residue locations relevant to anesthetic effects except for torpedo nAChR. Within the GABAaR models generated from GluCl, the residues notable for modulating anesthetic action within transmembrane segments 1, 2, and 3 converged on the intersubunit interface between ? and ? subunits. Docking scores of a propofol derivative series into this binding site showed strong linear correlation with GABAaR potentiation EC50. Conclusion: Consensus structural alignment based on homologous templates revealed an intersubunit anesthetic binding cavity within the transmembrane domain of the GABAaR, which showed a correlation of ligand docking scores with experimentally measured GABAaR potentiation.

Subject headings

NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Anestesi och intensivvård (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Anesthesiology and Intensive Care (hsv//eng)

Keyword

4 aminobutyric acid receptor
chloride channel
glutamic acid
nicotinic receptor alpha4
nicotinic receptor beta2
propofol
algorithm
analgesic activity
article
binding affinity
consensus
drug binding site
drug effect
drug protein binding
Gloeobacter violaceus
human
molecular docking
molecular model
nonhuman
Pectobacterium chrysanthemi
pH
priority journal
prokaryote
protein structure
sequence alignment

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ref (subject category)
art (subject category)

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Bertaccini, E. J ...
Yoluk, Özge
Lindahl, Erik R.
Trudell, James R ...
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NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
and Biophysics
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Anesthesiology a ...
Articles in the publication
Anesthesiology
By the university
Royal Institute of Technology

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