Interphotoreceptor retinoid-binding protein (IRBP) transports 11-cis and all-trans retinoids between the RPE and photoreceptors by solubilizing retinoids and enhancing the release of 11-cis retinal from the RPE. The long-term goal is to understand the mechanisms by which IRBP fulfills these tasks. IRBP consists of four homologous modules each containing two hydrophobic ligand-binding sites and a non-ligand-binding region that is a candidate docking site for an interphotoreceptor matrix or cell surface receptor. It is reasoned that through gene duplication the structure of the modules diverged, creating sites tailored for each of IRBP's physiological ligands. The working hypothesis is that through gene duplication and divergence the modules obtained binding sites tailored for different ligands as well as domains that interact with the matrix or cell surface.
Three specific aims are proposed: (1) The hypothesis predicts that IRBP possesses two classes of modules, each preferentially binding different ligand sets. The ligand affinity and specificity of each module will be compared with that of the full-length IRBP and selected module combinations. This will be complemented by mutagenesis studies of a single module. The two binding sites within the module will be characterized through Arg to Gln and Trp to Phe substitutions. (2) The structural requirements for IRBP's function will be determined under physiological conditions. Using eyecup preparations, IRBP, the individual modules, selected module combinations and truncated modules will be assessed for ability to support rhodopsin regeneration, and the delivery and release of retinoids at the RPE apical surface. Full physiological activity of IRBP may require combinations of modules, and non-ligand-binding regions that could be receptor-docking sites. (3) The X-ray crystal structure of an individual IRBP module will be determined. The size of an individual IRBP module, the functional unit of IRBP, is ideal for X-ray crystallography. Preliminary studies indicate that crystals of IRBP module 2 will be of sufficient quality to solve the structure of an individual module. Insights gained from the crystal structure will suggest further functional studies for future work.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY009412-08
Application #
6384341
Study Section
Visual Sciences C Study Section (VISC)
Program Officer
Mariani, Andrew P
Project Start
1993-07-01
Project End
2002-07-31
Budget Start
2001-08-01
Budget End
2002-07-31
Support Year
8
Fiscal Year
2001
Total Cost
$168,469
Indirect Cost
Name
University of Virginia
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
001910777
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Gonzalez-Fernandez, Federico; Fornalik, Mark; Garlipp, Mary Alice et al. (2018) Pericellular interphotoreceptor matrix dictates outer retina critical surface tension. Exp Eye Res 167:163-173
Chen, Chunhe; Adler 4th, Leopold; Goletz, Patrice et al. (2017) Interphotoreceptor retinoid-binding protein removes all-trans-retinol and retinal from rod outer segments, preventing lipofuscin precursor formation. J Biol Chem 292:19356-19365
Betts-Obregon, B S; Mondragon, A A; Mendiola, A S et al. (2016) TGF? induces BIGH3 expression and human retinal pericyte apoptosis: a novel pathway of diabetic retinopathy. Eye (Lond) 30:1639-1647
Ghosh, Debashis; Haswell, Karen M; Sprada, Molly et al. (2016) Fold conservation and proteolysis in zebrafish IRBP structure: Clues to possible enzymatic function? Exp Eye Res 147:78-84
Patel, Sangita P; Schaefer, Jamie L; Jaber, Ryan et al. (2016) The Value of Cytology Smears for Acanthamoeba Keratitis. Case Rep Ophthalmol Med 2016:4148968
Gonzalez-Fernandez, Federico; Betts-Obregon, Brandi; Tsin, Andrew T et al. (2016) Technical brief: Pump-probe paradigm in an integrating cavity to study photodecomposition processes. Mol Vis 22:953-8
Ghosh, Debashis; Haswell, Karen M; Sprada, Molly et al. (2015) Structure of zebrafish IRBP reveals fatty acid binding. Exp Eye Res 140:149-158
Gonzalez-Fernandez, Federico; Betts-Obregon, Brandi; Yust, Brian et al. (2015) Interphotoreceptor retinoid-binding protein protects retinoids from photodegradation. Photochem Photobiol 91:371-8
Gonzalez-Fernandez, Federico; Sung, Dongjin; Haswell, Karen M et al. (2014) Thiol-dependent antioxidant activity of interphotoreceptor retinoid-binding protein. Exp Eye Res 120:167-74
Sane, M; Selvadurai, A; Reidy, J et al. (2014) Transient visual loss due to reversible 'pending' central retinal artery occlusion in occult giant cell arteritis. Eye (Lond) 28:1387-90

Showing the most recent 10 out of 20 publications