This project will provide fundamental information on the structure and function of several types of neuroreceptors and ion channels (receptors). These are the fundamental molecules of the brain an nervous system. They are athe crucial structures associated with many disease states and are the targets of many therapeutic approaches. The work will employ a new tool recently developed in these labs - the ability to incorporate unnatural amino acids at specific sites in th receptors and to express the proteins in intact cells. When coupled with modern electrophysiological methods, this allows study of structure and function with unprecedented precision. In particular, the first target system will be the nicotinic acetylcholine receptor. This is a prototype neuroreceptor and is representative of a broad class of important structures. The investigations will reveal the manner in which ligands (agonists and antagonists) interact with the receptor and produce the characteristic gating response. These studies will also lead to the development of geometrical information concerning the overall layout of the protein . When coupled with modern computer modeling techniques, this will produce viable, three-dimensional structures for this class of receptors. The second target system will be the voltage-gated potassium channels and related structures. Again, both information on channel function and precise geometrical models will be developed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS034407-04
Application #
2735671
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Baughman, Robert W
Project Start
1995-07-01
Project End
1999-06-30
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
4
Fiscal Year
1998
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Engineering
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Mosesso, Richard; Dougherty, Dennis A (2018) A triad of residues is functionally transferrable between 5-HT3 serotonin receptors and nicotinic acetylcholine receptors. J Biol Chem 293:2903-2914
Post, Michael R; Tender, Gabrielle S; Lester, Henry A et al. (2017) Secondary Ammonium Agonists Make Dual Cation-? Interactions in ?4?2 Nicotinic Receptors. eNeuro 4:
Post, Michael R; Lester, Henry A; Dougherty, Dennis A (2017) Probing for and Quantifying Agonist Hydrogen Bonds in ?6?2 Nicotinic Acetylcholine Receptors. Biochemistry 56:1836-1840
Rienzo, Matthew; Rocchi, Angela R; Threatt, Stephanie D et al. (2016) Perturbation of Critical Prolines in Gloeobacter violaceus Ligand-gated Ion Channel (GLIC) Supports Conserved Gating Motions among Cys-loop Receptors. J Biol Chem 291:6272-80
Nichols, Weston A; Henderson, Brandon J; Marotta, Christopher B et al. (2016) Mutation Linked to Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Reduces Low-Sensitivity ?4?2, and Increases ?5?4?2, Nicotinic Receptor Surface Expression. PLoS One 11:e0158032
Davis, Matthew R; Dougherty, Dennis A (2015) Cation-? interactions: computational analyses of the aromatic box motif and the fluorination strategy for experimental evaluation. Phys Chem Chem Phys 17:29262-70
Henderson, Brandon J; Lester, Henry A (2015) Inside-out neuropharmacology of nicotinic drugs. Neuropharmacology 96:178-93
Marotta, Christopher B; Lester, Henry A; Dougherty, Dennis A (2015) An Unaltered Orthosteric Site and a Network of Long-Range Allosteric Interactions for PNU-120596 in ?7 Nicotinic Acetylcholine Receptors. Chem Biol 22:1063-73
Post, Michael R; Limapichat, Walrati; Lester, Henry A et al. (2015) Heterologous expression and nonsense suppression provide insights into agonist behavior at ?6?2 nicotinic acetylcholine receptors. Neuropharmacology 97:376-82
Miles, Timothy F; Lester, Henry A; Dougherty, Dennis A (2015) Allosteric activation of the 5-HT3AB receptor by mCPBG. Neuropharmacology 91:103-8

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