Cardiovascular disease (CVD) is the number one killer disease in the USA talking nearly a million lives each year. It is well established that high density lipoprotein (HDL) and its major protein constituent apolipoprotein (apo) A-l play a major role in reducing the risk of CVD. However the function of ApoA-ll, the second most abundant protein in HDL, has not been determined. Studies on apoA-ll have lead to mixed conclusions concerning the pro- or anti-atherogenicity of apoA-ll in HDL. This study will test the hypothesis that apoA-ll interacts with apoA-l in HDL in a site-specific manner to modulate its function. Furthermore, the effect is based on the relative amounts of apoA-l: apoA-ll present in a given HDL particle. In the mentored phase of this project, we will determine how the incorporation of apoA-ll affects apoA-l structure in discbidal reconstituted HDL particles. Relative changes in the solvent accessibility^ of specific apoA-l sequences in mixed particles vs apoA-| only HDL will assessed using the hydrogen deuterium exchange technique combined with mass spectrometry (HDX-MS). We will then extend our studies, in the independent phase, to locate conformational changes in apoA-l caused by apoA-ll in HDL particles from human plasma. This will be accomplished in stages. First, we will reconstitute spherical HDL particles that resemble native HDL by incorporating varying ratios of apoA-l:apoA-ll along with native HDL lipids. We will also generate native hybrid HDL particles by incorporating isolated apoA-ll into native HDL containing apoA-l only. The apoA-ll induced modifications of apoA-l solvent exposure will then be conrelated to functional properties including activation of various HDL remodeling factors including lecithin:cholesterol acyl transferase (LCAT), cholesteryl ester transfer protein (CETP), hepatic lipase, and endothelial lipase, in addition, receptor interactions with cubilin will be monitored. We anticipate that this work will provide significant new information on the role of apoA-il in lipoprotein metabolism and may suggest new therapeutic approaches for fighting CVD.

Public Health Relevance

HDL and its major protein component apoA-l have been shown to play a major beneficial role in decreasing the risk of cardiovascular disease. However, the current understanding of functional roles of apoA-ll, the second major protein in HDL is at a basic level. Our proposal that focuses on apoA-ll modulation of apoA-l- HDL fijnction will provide important new infomriation on the stmcture-fundion correlations and may form the basis for new therapeutic targets for enhancing HDL protective function.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Transition Award (R00)
Project #
5R00HL087561-05
Application #
8013329
Study Section
Special Emphasis Panel (NSS)
Program Officer
Liu, Lijuan
Project Start
2009-01-12
Project End
2012-08-31
Budget Start
2011-01-01
Budget End
2012-08-31
Support Year
5
Fiscal Year
2011
Total Cost
$248,999
Indirect Cost
Name
University of Cincinnati
Department
Pathology
Type
Schools of Medicine
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Gauthamadasa, Kekulawalage; Vaitinadin, Nataraja Sarma; Dressman, James L et al. (2012) Apolipoprotein A-II-mediated conformational changes of apolipoprotein A-I in discoidal high density lipoproteins. J Biol Chem 287:7615-25
Smith, Loren E; Yang, Jun; Goodman, Leah et al. (2012) High yield expression and purification of recombinant human apolipoprotein A-II in Escherichia coli. J Lipid Res 53:1708-15
Gauthamadasa, Kekulawalage; Rosales, Corina; Pownall, Henry J et al. (2010) Speciated human high-density lipoprotein protein proximity profiles. Biochemistry 49:10656-65