Although circulating high density lipoproteins (HDL) are considered protective from cardiovascular disease, we have a remarkably limited understanding of their structure. Furthermore, we understand even less about how the major HDL protein, apolipoprotein (apo)A-I, interacts with other proteins to dictate HDL function. This project will test the hypothesis that apoA-I makes highly specific contacts with it and other HDL associated proteins in spherical HDL particles commonly found in human plasma. In our previous work, we used cross- linking chemistry and mass spectrometry to generate detailed models of apoA-I in reconstituted particles as well as """"""""real"""""""" HDL from human plasma. Despite substantial differences in size and shape, these structures all shared the theme of an antiparallel belt-like arrangement. Building on these discoveries, our goal is to further evaluate these and other models using complementary structural techniques as well as evaluate the basis of apoA-I's interactions with three major HDL components: apolipoprotein A-II, lecithin:cholesterol acyl transferase (LCAT), and cholesteryl ester transfer protein (CETP).
The specific aims are: 1) To test the Trefoil-based models of apoA-I in spherical reconstituted and native plasma HDL using new dual isotope cross-linking techniques and state-of-the-art all-atom and course grained molecular dynamics (MD) techniques. 2) To determine the molecular interactions between apoA-I and apoA-II using cross-linking and a new human apoA-II bacterial expression system to derive the first models of native HDL particles containing both proteins. 3) To determine the molecular interaction between apoA-I and LCAT by testing the concept that LCAT accesses a molecular pore in the apoA-I structure using site-directed mutagenesis and cross-linking. We will also determine if CETP specifically binds apoA-I and identify their points o contact. This approach uniquely intertwines new experimental techniques with state-of-the-art MD approaches that will magnify our structural understanding of these enigmatic particles. The structure of apoA-I undoubtedly modulates HDL metabolism. Thus, a molecular understanding of its structure and its interactions with other proteins, particularly those being explored as dru targets such as LCAT and CETP, is critical for the design of new therapies exploiting reverse cholesterol transport and the anti-inflammatory roles of HDL.

Public Health Relevance

The proposed research is relevant to public health because an increased understanding of the function of high density lipoproteins (HDL) will help guide the development of therapeutic strategies designed to raise plasma HDL for protection against cardiovascular disease, the # 1 killer in the U.S. Thus, the proposed research is relevant to the part of NIH's mission that pertains to developing fundamental knowledge for understanding the causes, prevention and eventually a cure for human diseases.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Research Project (R01)
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Special Emphasis Panel (ZRG1)
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Liu, Lijuan
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University of Cincinnati
Schools of Medicine
United States
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Davidson, W Sean; Heink, Anna; Sexmith, Hannah et al. (2017) Obesity is associated with an altered HDL subspecies profile among adolescents with metabolic disease. J Lipid Res 58:1916-1923
Davidson, W S; Inge, T H; Sexmith, H et al. (2017) Weight loss surgery in adolescents corrects high-density lipoprotein subspecies and their function. Int J Obes (Lond) 41:83-89
Rosales, C; Davidson, W S; Gillard, B K et al. (2016) Speciated High-Density Lipoprotein Biogenesis and Functionality. Curr Atheroscler Rep 18:25
Melchior, John T; Walker, Ryan G; Morris, Jamie et al. (2016) An Evaluation of the Crystal Structure of C-terminal Truncated Apolipoprotein A-I in Solution Reveals Structural Dynamics Related to Lipid Binding. J Biol Chem 291:5439-51
Davidson, W Sean; Heink, Anna; Sexmith, Hannah et al. (2016) The effects of apolipoprotein B depletion on HDL subspecies composition and function. J Lipid Res 57:674-86
Gordon, Scott M; Li, Hailong; Zhu, Xiaoting et al. (2016) Impact of genetic deletion of platform apolipoproteins on the size distribution of the murine lipoproteome. J Proteomics 146:184-94
Heink, Anna; Davidson, W Sean; Swertfeger, Debi K et al. (2015) A Comparison of Methods To Enhance Protein Detection of Lipoproteins by Mass Spectrometry. J Proteome Res 14:2943-50
Deng, Xiaodi; Walker, Ryan G; Morris, Jamie et al. (2015) Role of Conserved Proline Residues in Human Apolipoprotein A-IV Structure and Function. J Biol Chem 290:10689-702
Unruh, Dusten; Srinivasan, Ramprasad; Benson, Tyler et al. (2015) Red Blood Cell Dysfunction Induced by High-Fat Diet: Potential Implications for Obesity-Related Atherosclerosis. Circulation 132:1898-908
Gordon, Scott M; Li, Hailong; Zhu, Xiaoting et al. (2015) A comparison of the mouse and human lipoproteome: suitability of the mouse model for studies of human lipoproteins. J Proteome Res 14:2686-95

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