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1 December 2004 Structural Requirements for Efficient Cellular Photoprotection by Carotenoid Derivatives
Jeffrey R. Kanofsky, Paul D. Sima
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We have synthesized five carotenoid derivatives: (1) Girard's reagent P (GRP)-retinal from GRP and retinal; (2) GRP-carotenal from GRP and β-apo-8′-carotenal; (3) Girard's reagent T (GRT)-carotenal from GRT and β-apo-8′-carotenal; (4) (GRP)2-canthaxanthin from 2 mol of GRP and 1 mol of canthaxanthin; and (5) dansyl hydrazine (DH)-carotenal from DH and β-apo-8′-carotenal. The first three derivatives are cations, whereas the fourth is a dication and the fifth is a weak base. Using K562 cells, we compared the subcellular distribution of the synthetic carotenoid derivatives with two uncharged natural carotenoids, β-carotene and β-apo-8′-carotenal. The two natural carotenoids were present mainly within the cell membranes. The synthetic carotenoid derivatives were more broadly distributed among the cell organelles. The positively charged derivatives had relatively high concentrations in mitochondria, whereas DH-carotenal had a relatively high concentration in lysosomes. We also measured the amount of photoprotection provided by the synthetic and natural carotenoids for K562 cells labeled with a photosensitizer (hypericin, protoporphyrin IX or cis-di[4-sulfonatophenyl]diphenylporphine). In this model system, only carotenoid derivatives with a permanent positive charge provided significant photoprotection. Neither the two natural carotenoids nor DH-carotenal were effective photoprotectors.

Jeffrey R. Kanofsky and Paul D. Sima "Structural Requirements for Efficient Cellular Photoprotection by Carotenoid Derivatives," Photochemistry and Photobiology 80(3), 507-517, (1 December 2004).<0507:SRFECP>2.0.CO;2
Received: 2 December 2003; Accepted: 1 August 2004; Published: 1 December 2004

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