The Program Project Grant Structure and Function of Mechanosensitive Ion Channels brings together an array of technologies drawn from chemistry, biology, physics, and biotechnology to develop the most detailed structure/function analysis of an ion channel protein to date. Building on the foundation of the high resolution crystal structure of the Tb-MscL channel reported by Rees, the tools of structural biology, organic chemistry, determine how a channel responds to a stimulus and translates that stimulus into an observable signal. The four key components of the proposed program are: structure, function, synthesis, and redesign, and each of the parent MscL channel and on selected variants with the ultimate goal being a structure determination of the open state of the channel. High resolution electrophysiology techniques will correlate structure and function, and single molecule spectroscopy will provide unprecedented views of ion behavior. For the first time, total diversity involving both natural and unnatural modifications. A high throughput assay for MscL behavior will greatly aid the analysis of the structural variants prepared, and computer modeling will provide detailed insights into experimental observations. Since ion channels lie at the core of molecular neurobiology, the information obtained from this Project Grant will have far-reaching consequences. The list of neurological disorders associated with a malfunction in an ion channel protein is long and growing, and the information obtained here will be invaluable in understanding such disease states and in developing effective treatment strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Program Projects (P01)
Project #
5P01GM062532-03
Application #
6525996
Study Section
Special Emphasis Panel (ZRG1-MCHA (01))
Program Officer
Chin, Jean
Project Start
2000-09-30
Project End
2005-08-31
Budget Start
2002-09-01
Budget End
2003-08-31
Support Year
3
Fiscal Year
2002
Total Cost
$882,675
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Engineering
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
Elmore, Donald E (2010) Bringing ion channel crystal structures into sharper focus with computer modeling: examples from mechanosensitive channels. Future Med Chem 2:909-13
Maurer, Joshua A; Elmore, Donald E; Clayton, Daniel et al. (2008) Confirming the revised C-terminal domain of the MscL crystal structure. Biophys J 94:4662-7
Maurer, Joshua A; White, Victor E; Dougherty, Dennis A et al. (2007) Reconstitution of ion channels in agarose-supported silicon orifices. Biosens Bioelectron 22:2577-84
Spronk, Steven A; Elmore, Donald E; Dougherty, Dennis A (2006) Voltage-dependent hydration and conduction properties of the hydrophobic pore of the mechanosensitive channel of small conductance. Biophys J 90:3555-69
Kochendoerfer, Gerd G; Clayton, Daniel; Becker, Christian (2005) Chemical synthesis approaches to the engineering of ion channels. Protein Pept Lett 12:737-41
Becker, Christian F W; Strop, Pavel; Bass, Randal B et al. (2004) Conversion of a mechanosensitive channel protein from a membrane-embedded to a water-soluble form by covalent modification with amphiphiles. J Mol Biol 343:747-58
Becker, Christian F W; Clayton, Daniel; Shapovalov, George et al. (2004) On-resin assembly of a linkerless lanthanide(III)-based luminescence label and its application to the total synthesis of site-specifically labeled mechanosensitive channels. Bioconjug Chem 15:1118-24
Shapovalov, George; Lester, Henry A (2004) Gating transitions in bacterial ion channels measured at 3 microns resolution. J Gen Physiol 124:151-61
Kochendoerfer, Gerd G; Jones, David H; Lee, Sangwon et al. (2004) Functional characterization and NMR spectroscopy on full-length Vpu from HIV-1 prepared by total chemical synthesis. J Am Chem Soc 126:2439-46
Clayton, Daniel; Shapovalov, George; Maurer, Joshua A et al. (2004) Total chemical synthesis and electrophysiological characterization of mechanosensitive channels from Escherichia coli and Mycobacterium tuberculosis. Proc Natl Acad Sci U S A 101:4764-9

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