This competing renewal application seeks continued support for a primary research in the Pi's laboratory using the computational approaches to elucidating the molecular mechanisms of general anesthesia. Research in the previous funding period challenged the traditional structure-function paradigm in explaining the action of general anesthetics on ion channel proteins (Tang&Xu, PNAS, 99:16035-16040, 2002) and proposed an alternative viewpoint that the effects of general anesthetics on protein global dynamics on the timescale matching the characteristic time of protein function might underlie a common mechanism of action of general anesthetics. To test this central hypothesis, we will take 4x4 approach to integrate 4 complementary state- of-the-art computational methods with 4 levels of validation with experimental data. We will focus on the anesthetic-hypersensitive neuronal (04)2(32)3 nicotinic acetylcholine receptor (nAChR) and the anesthetic- insensitive (a7)5 nAChR, as well as the Torpedo isoform of the muscle-type (alkplvQ nAChR. A novel integration of homology modeling, molecular dynamics (MD) simulations in a fully hydrated ternary membrane patch, coarse-grained normal mode analysis (NMA), and Brownian dynamics (BD) will be used to generate and validate high-resolution, closed and putatively open structural models for (alkpIvS, (a4)2(p2)3 and (a7)5 nAChR on the basis of the 4-A resolution structure of the (a1)2p1v5 nAChR as a template. Flexible ligand docking or manual docking of anesthetics (halothane and isoflurane) at experimentally identified anesthetic-binding sites will be followed by MD equilibration to encode anesthetic effects on tertiary and quaternary structures. NMA and BD will then be used to quantify the gating-related low-frequency motions of the receptors and ion permeation across the channel. Two groups of mutations that changed nAChR's sensitivity to anesthetics experimentally will be tested for global dynamics changes. Four levels of experimental validation for structures will include agonist- binding affinity, topology matching to low-resolution experimental structures and pore residue accessibilities, I-V curve calculations, and cation/anion and mono-/di-valence ion permeability ratios. Our substantive amount of preliminary results supports the following four specific aims: (1) To generate and validate, using existing experimental data, the closed- and putative open-channel structures of the neuronal (a4)2(p2)3 nAChR (hypersensitive to volatile anesthetics) and (a7)5 nAChR (insensitive to volatile anesthetics) as well as the open- channel structure for Torpedo (al^plvfi nAChR (sensitive to volatile anesthetics);(2) To perform extensive, multi-seed MD simulations on wild type and mutant channels in the absence and presence of anesthetics;(3) To carry out normal mode analysis to determine anesthetic effects on global dynamics, using the fully equilibrated structures in SA#2 as input;and (4) To relate anesthetic effects on global dynamics to channel function by performing Brownian dynamics calculations of ion permeation through the putative open-channels. The research will bridge the experimental and theoretical understanding of anesthetic effects on channel proteins, thereby facilitating the future design of new and novel anesthetic drugs that are more specific with fewer side effects.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM066358-07
Application #
7535211
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Program Officer
Cole, Alison E
Project Start
2002-07-01
Project End
2010-11-30
Budget Start
2008-12-01
Budget End
2009-11-30
Support Year
7
Fiscal Year
2009
Total Cost
$303,439
Indirect Cost
Name
University of Pittsburgh
Department
Anesthesiology
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Tang, Pei; Eckenhoff, Roderic (2018) Recent progress on the molecular pharmacology of propofol. F1000Res 7:123
Ion, Bogdan F; Wells, Marta M; Chen, Qiang et al. (2017) Ketamine Inhibition of the Pentameric Ligand-Gated Ion Channel GLIC. Biophys J 113:605-612
Chen, Qiang; Wells, Marta M; Tillman, Tommy S et al. (2017) Structural Basis of Alcohol Inhibition of the Pentameric Ligand-Gated Ion Channel ELIC. Structure 25:180-187
Stollings, Lindsay M; Jia, Li-Jie; Tang, Pei et al. (2016) Immune Modulation by Volatile Anesthetics. Anesthesiology 125:399-411
Wu, Jie; Liu, Qiang; Tang, Pei et al. (2016) Heteromeric ?7?2 Nicotinic Acetylcholine Receptors in the Brain. Trends Pharmacol Sci 37:562-574
Tillman, Tommy S; Alvarez, Frances J D; Reinert, Nathan J et al. (2016) Functional Human ?7 Nicotinic Acetylcholine Receptor (nAChR) Generated from Escherichia coli. J Biol Chem 291:18276-82
Kinde, Monica N; Bu, Weiming; Chen, Qiang et al. (2016) Common Anesthetic-binding Site for Inhibition of Pentameric Ligand-gated Ion Channels. Anesthesiology 124:664-73
Kinde, Monica N; Chen, Qiang; Lawless, Matthew J et al. (2015) Conformational Changes Underlying Desensitization of the Pentameric Ligand-Gated Ion Channel ELIC. Structure 23:995-1004
Chen, Qiang; Kinde, Monica N; Arjunan, Palaniappa et al. (2015) Direct Pore Binding as a Mechanism for Isoflurane Inhibition of the Pentameric Ligand-gated Ion Channel ELIC. Sci Rep 5:13833
Zhou, David W; Mowrey, David D; Tang, Pei et al. (2015) Percolation Model of Sensory Transmission and Loss of Consciousness Under General Anesthesia. Phys Rev Lett 115:108103

Showing the most recent 10 out of 49 publications