CaltechTHESIS
  A Caltech Library Service

Structure-function studies of Drosophila shaker potassium channels

Citation

McCormack, Ken (1991) Structure-function studies of Drosophila shaker potassium channels. Dissertation (Ph.D.), California Institute of Technology. http://resolver.caltech.edu/CaltechETD:etd-07182007-074159

Abstract

Voltage-dependent ion channels mediate electrical signals in the nervous system; many sodium (Na+), calcium (Ca++) and potassium (K+) selective channels are structurally related, and thus represent a family. These proteins undergo interesting conformational changes in response to alterations in transmembrane potential. However, the functional determinants involved in these transitions are not well understood. Chapters 2A and 2B describe the identification and characterization of an amino acid sequence motif (a leucine-heptad repeat) that is evolutionarily conserved among this family of voltage-dependent ion channels. Conservative, single amino-acid substitutions within this region of Drosophila Shaker (Sh) proteins have substantial effects on the voltage-dependence of activation. The observed alterations suggest that the heptad-repeat region is an important determinant in the conformational transitions leading to channel opening.

Na+ and Ca++ channels are composed of four homologous domains, each of which is equivalent to a single K+ channel subunit. Thus, K+ channels are thought to be functional multimers. Furthermore, there are a large number of different voltage-dependent K+ genes and alternatively spliced products that potentially can be expressed in the same cell. Therefore, the potential number of different K+ channel multimers could be quite extensive. Chapter 3 describes the physiological characteristics of combinations of K+ channels belonging to the Sh family that have been coexpressed in Xenopus oocytes. Members of the same molecular class of Sh channel form heteromultimers with novel functional properties, adding to the diversity of K+ channel function. Members of different molecular classes do not form heteromultimeric channels, suggesting that there are distinct K+ channel systems. The Appendix describes an alternative exon in the "constant" region of the Drosophila Sh gene, the existence of which suggests, that the molecular diversity of this gene is greater than previously determined.

Item Type:Thesis (Dissertation (Ph.D.))
Degree Grantor:California Institute of Technology
Division:Biology
Major Option:Biology
Thesis Availability:Restricted to Caltech community only
Research Advisor(s):
  • Tanouye, Mark
Thesis Committee:
  • Tanouye, Mark (chair)
  • Lester, Henry A.
  • Davidson, Norman R.
Defense Date:7 March 1991
Record Number:CaltechETD:etd-07182007-074159
Persistent URL:http://resolver.caltech.edu/CaltechETD:etd-07182007-074159
Default Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:2922
Collection:CaltechTHESIS
Deposited By: Imported from ETD-db
Deposited On:02 Aug 2007
Last Modified:26 Dec 2012 02:55

Thesis Files

[img] PDF (McCormack_k_1991.pdf) - Final Version
Restricted to Caltech community only
See Usage Policy.

4Mb

Repository Staff Only: item control page