This grant request is focused on how 11-cis retina is biosynthesized in the retina/pigmented epithelium of vertebrate animals. The question of how this process occurs is formulated in two separate but coupled ways. The first objective is to determine the mechanism of 11-cis retinal biosynthesis. Of great importance here is to determine whether the isomerization of an all trans retinoid to an 11-cis retinoid is enzyme-mediated or not. The second objective is to determine where the energy comes from for the biosynthesis of the 11-cis retinoids. In a dark adapted eye, greater than 75% of the retinoids can be in the 11-cis form, whereas at equilibrium, only 0.1% is in the 11-cis form. The formation of equal quantities of 11-cis and all-trans retinoids requires the input of approximately 4 kcal/mol. The question of the mechanism of 11-cis retinoid formation will be approached by determining 1) the in vivo stereospecificity of the isomerization process, 2) which all-trans retinoid is isomerized, and 3) whether any evidence for the material presence of a retinoid isomerase can be obtained. If evidence for an enzyme is found, the enzyme will be purified and characterized. Whether an isomerase enzyme exists or not, energy source for the production of 11-cis retinoid must be found. Our ultimate goal here is to determine whether the 11-cis retinal(o1) binding protein can provide the energy or whether an ATP-dependent mechanism might be involved. The research alluded to here could be of importance in understanding the etiology of certain forms of night blindness and retinitis pigmentosa.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004096-08
Application #
3258576
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1982-04-01
Project End
1990-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
8
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Fishkin, Nathan; Yefidoff, Revital; Gollipalli, Deviprasad R et al. (2005) On the mechanism of isomerization of all-trans-retinol esters to 11-cis-retinol in retinal pigment epithelial cells: 11-fluoro-all-trans-retinol as substrate/inhibitor in the visual cycle. Bioorg Med Chem 13:5189-94
Xue, Linlong; Rando, Robert R (2004) Roles of cysteine 161 and tyrosine 154 in the lecithin-retinol acyltransferase mechanism. Biochemistry 43:6120-6
Xue, Linlong; Gollapalli, Deviprasad R; Maiti, Pranab et al. (2004) A palmitoylation switch mechanism in the regulation of the visual cycle. Cell 117:761-71
Gollapalli, Deviprasad R; Rando, Robert R (2004) The specific binding of retinoic acid to RPE65 and approaches to the treatment of macular degeneration. Proc Natl Acad Sci U S A 101:10030-5
Gollapalli, Deviprasad R; Rando, Robert R (2003) Molecular logic of 11-cis-retinoid biosynthesis in a cone-dominated species. Biochemistry 42:14921-9
Krosky, Paula M; Baek, Moon-Chang; Jahng, Wan Jin et al. (2003) The human cytomegalovirus UL44 protein is a substrate for the UL97 protein kinase. J Virol 77:7720-7
Jahng, Wan Jin; Xue, Linlong; Rando, Robert R (2003) Lecithin retinol acyltransferase is a founder member of a novel family of enzymes. Biochemistry 42:12805-12
Gollapalli, Deviprasad R; Maiti, Pranab; Rando, Robert R (2003) RPE65 operates in the vertebrate visual cycle by stereospecifically binding all-trans-retinyl esters. Biochemistry 42:11824-30
Gollapalli, Deviprasad R; Rando, Robert R (2003) All-trans-retinyl esters are the substrates for isomerization in the vertebrate visual cycle. Biochemistry 42:5809-18
Bok, Dean; Ruiz, Alberto; Yaron, Orna et al. (2003) Purification and characterization of a transmembrane domain-deleted form of lecithin retinol acyltransferase. Biochemistry 42:6090-8

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