The lipid landscape of cellular membranes changes with the development of disease such as infantile congenital heart failure, hypertension, and Alzheimer's. Also associated with these diseases are ionic currents passing through ion channels that regulate excitability in these cells. The intimate interaction of ion channels with te cell membrane is a major determinant of function, yet is not well characterized. Inwardly rectifying potassium (IKir) currents, found in cardiac myocytes and many other excitable cells play a vital role in setting the membrane potential and modulating membrane excitability. Until recently, analyses of lipid regulation of mammalian Kir2.1 and Kir2.2 ion channels were largely qualitative since these studies could only be performed in cells, where lipid composition is complex, difficult to control, and poorly understood. Biochemical properties of human Kir channels inferred from analysis performed on their bacterial homologues are limited since they share only ~30% sequence identity and are regulated differently by some membrane lipids. Thus, until recently, biochemical and structural analyses on eukaryotic Kir channels remained elusive. However, the PI has recently made a critical breakthrough in being able to express and purify functional human Kir channels in yeast. This breakthrough opens up several important avenues to understand regulation of Kir channels, as proposed in Aim 1 of this proposal. The expertise developed will then be used to assess the role of lipids in modulating representative members of two other K+ permeating channel sub-families (Kv1.2-2.1 and HCN channels) with topological and functional characteristics distinct from the Kir channel family (Aim 2). These particular sub-families have been selected for examination because of their important physiological role and, because despite some evidence that they may also be regulated by membrane lipids, little is known about lipid modulation of these channels. Thus, using a unique combination of biochemical techniques, 86Rb+ flux assays, electrophysiology, and molecular dynamics simulations, these two specific aims will address the unifying question: What are the molecular determinants and mechanisms by which lipids regulate K+ channels?

Public Health Relevance

The lipid landscape of cellular membranes changes with the development of disease such as infantile congenital heart failure, hypertension, and Alzheimer's, as does the excitability of the cells in the affected tissue. Ion channels (such as potassium channels) that drive cellular excitability are intimately surrounded by lipids in the cell membrane, yet how these channels are regulated by the lipid properties has not been thoroughly examined. Understanding the interplay between lipids and potassium channel proteins presents an exciting emerging field of study and will establish a new paradigm in our understanding of the development and treatment of such diseases.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Career Transition Award (K99)
Project #
1K99HL112300-01
Application #
8223716
Study Section
Special Emphasis Panel (ZHL1-CSR-P (O2))
Program Officer
Carlson, Drew E
Project Start
2012-01-01
Project End
2012-04-30
Budget Start
2012-01-01
Budget End
2012-04-30
Support Year
1
Fiscal Year
2012
Total Cost
$46,818
Indirect Cost
$3,468
Name
Washington University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
D'Avanzo, Nazzareno; McCusker, Emily C; Powl, Andrew M et al. (2013) Differential lipid dependence of the function of bacterial sodium channels. PLoS One 8:e61216
D'Avanzo, Nazzareno; Lee, Sun-Joo; Cheng, Wayland W L et al. (2013) Energetics and location of phosphoinositide binding in human Kir2.1 channels. J Biol Chem 288:16726-37