Hydrolysis of triacylglycerols by lipoprotein lipase (LPL) is essential for normal lipidmetabolism. LPL does not fold and function properly without a newly identified,transmembrane protein, lipase maturation factor (LMF1). LMF1 is essentiallyuncharacterized; in fact it belongs to a family of proteins with a similar 'domain ofunknown function' (Duf1222). The major goal of this project is to investigate theinteraction between LPL and LMF1. By analogy to lipases with structural characteristicssimilar to LPL, we propose that LMF1 acts as a 'private foldase' for LPL.
In Aim 1, I willuse biochemical assays and assays in cells to determine why LPL needs foldingassistance and how LMF1 helps LPL fold.
Aim 2 consists of analysis of the membranetopology and structure of LMF1. Finally, Aim 3 focuses on the observation that manyhuman pathogens have Duf1222 proteins; therefore I will use computational andbiochemical approaches to determine if the Duf1222 protein represents one-half of afoldase-lipase pair. During the mentored phase, I will build on my preliminaryobservations to develop a model for LMF1 membrane topology. Additionally I will beginbiochemical and structural analyses of the LMF-LPL interaction, and begin preliminarywork on aim 3. For the independent phase, I will continue structural analysis of LMF1and expand my biochemical analysis to Duf1222 proteins in other species to determine ifthey have important roles in lipid metabolism.

Public Health Relevance

Cardiovascular disease is a leading cause of death in the developed world, and elevated blood triacylglycerol is a risk factor. LPL deficiency results in elevated blood triacylglycerol and disturbs overall lipid metabolism. LMF1 promotes LPL activity through a poorly understood process, and elucidation of this mechanism will provide a foundation to begin to ameliorate one cause of LPL deficiency.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Transition Award (R00)
Project #
4R00HL098277-02
Application #
8254664
Study Section
Special Emphasis Panel (NSS)
Program Officer
Liu, Lijuan
Project Start
2011-06-01
Project End
2014-05-31
Budget Start
2011-06-01
Budget End
2012-05-31
Support Year
2
Fiscal Year
2011
Total Cost
$248,999
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Biochemistry
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Roberts, Benjamin S; Babilonia-Rosa, Melissa A; Broadwell, Lindsey J et al. (2018) Lipase maturation factor 1 affects redox homeostasis in the endoplasmic reticulum. EMBO J 37:
Babilonia-Rosa, Melissa A; Neher, Saskia B (2014) Purification, cellular levels, and functional domains of lipase maturation factor 1. Biochem Biophys Res Commun 450:423-8