The proposed research is directed toward a detailed understanding of the structure and function of ion channels in biological membranes at the molecular level, and of the role of such channels in cell communication. Ion channels are important for the transmission of signals that allow a cell or tissue to communicate with its environment or with other parts of a multicomponent organism. This project takes a """"""""bottom-up"""""""" approach to the design and mechanism of action of ion channels, starting with a chemically defined """"""""baseline"""""""" system and then introducing a series of subtle chemical changes, some of which will significantly influence important channel properties, such as the ion selectivity, the voltage dependence, and the assembly of channels in membranes. For these types of experiments, the gramicidin family of membrane channels offers several advantages: (i) a known tertiary structure; (ii) a well defined and well characterized channel function; (iii) an amenability to amino acid sequence substitutions and other chemical modifications; and (iv) an amenability to biophysical methods that have been well established for characterizing both the structures and the functional properties of modified channels in relation to the parent channels. The proposed investigations of the gramicidin family of channels are aimed at further understanding of general principles that govern structure-function relationships for ion-selective membrane channels.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM034968-15
Application #
2177682
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1984-09-01
Project End
1996-08-31
Budget Start
1995-09-01
Budget End
1996-08-31
Support Year
15
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Arkansas at Fayetteville
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
191429745
City
Fayetteville
State
AR
Country
United States
Zip Code
72701
Siegel, D P; Cherezov, V; Greathouse, D V et al. (2006) Transmembrane peptides stabilize inverted cubic phases in a biphasic length-dependent manner: implications for protein-induced membrane fusion. Biophys J 90:200-11
Lundbaek, Jens A; Birn, Pia; Hansen, Anker J et al. (2004) Regulation of sodium channel function by bilayer elasticity: the importance of hydrophobic coupling. Effects of Micelle-forming amphiphiles and cholesterol. J Gen Physiol 123:599-621
Goforth, Robyn L; Chi, Aung K; Greathouse, Denise V et al. (2003) Hydrophobic coupling of lipid bilayer energetics to channel function. J Gen Physiol 121:477-93
de Planque, Maurits R R; Bonev, Boyan B; Demmers, Jeroen A A et al. (2003) Interfacial anchor properties of tryptophan residues in transmembrane peptides can dominate over hydrophobic matching effects in peptide-lipid interactions. Biochemistry 42:5341-8
Hwang, Tzyh-Chang; Koeppe 2nd, Roger E; Andersen, Olaf S (2003) Genistein can modulate channel function by a phosphorylation-independent mechanism: importance of hydrophobic mismatch and bilayer mechanics. Biochemistry 42:13646-58
de Planque, Maurits R R; Boots, Jan-Willem P; Rijkers, Dirk T S et al. (2002) The effects of hydrophobic mismatch between phosphatidylcholine bilayers and transmembrane alpha-helical peptides depend on the nature of interfacially exposed aromatic and charged residues. Biochemistry 41:8396-404
Strandberg, Erik; Morein, Sven; Rijkers, Dirk T S et al. (2002) Lipid dependence of membrane anchoring properties and snorkeling behavior of aromatic and charged residues in transmembrane peptides. Biochemistry 41:7190-8
van der Wel, Patrick C A; Strandberg, Erik; Killian, J Antoinette et al. (2002) Geometry and intrinsic tilt of a tryptophan-anchored transmembrane alpha-helix determined by (2)H NMR. Biophys J 83:1479-88
Demmers, J A; van Duijn, E; Haverkamp, J et al. (2001) Interfacial positioning and stability of transmembrane peptides in lipid bilayers studied by combining hydrogen/deuterium exchange and mass spectrometry. J Biol Chem 276:34501-8
Greathouse, D V; Goforth, R L; Crawford, T et al. (2001) Optimized aminolysis conditions for cleavage of N-protected hydrophobic peptides from solid-phase resins. J Pept Res 57:519-27

Showing the most recent 10 out of 58 publications