6533b7d4fe1ef96bd1263488

RESEARCH PRODUCT

Photobinding of Tiaprofenic Acid and Subprofen to Proteins and Cells: A Combined Study Using Radiolabeling, Antibodies and Laser Flash Photolysis of Model Bichromophores

Agustín LahozJosé V. CastellZaideth SarabiaMaría José Gómez-lechónIsabel M. MoreraJulia Pérez-prietoMiguel A. MirandaDaniel Hernández

subject

ChemistryStereochemistrySuprofenGeneral MedicinePlasma protein bindingPhotochemistryBiochemistryCell membranemedicine.anatomical_structureLabellingmedicineFlash photolysisPhysical and Theoretical ChemistryBinding siteTyrosineTiaprofenic acidmedicine.drug

description

Drug photoallergy is a matter of current concern. It involves the formation of drug-protein photoadducts (photoantigens) that may ultimately trigger an immunological response. Tyrosine residues appear to be key binding sites in proteins. The present work has investigated the photobinding of tiaprofenic and (TPA) and the closely related isomer suprofen (SUP) to proteins and cells by means of radioactive labeling and drug-directed antibodies. To ascertain whether preassociation with the protein may play a role in photoreactivity, two model bichromophoric compounds (TPA-Tyr and SUP-Tyr) have been prepared and studied by laser flash photolysis. The results of this work show that (a) TPA and SUP photo-bind to proteins with similar efficiencies, (b) both drugs form photoadducts that share a basic common structure, as they are recognized by the same antibody and (c) drug-protein preassociation must play a key role in photoreactivity, as indicated by the dramatic decrease in the triplet state lifetimes of the model bichromophores compared to the parent drugs.

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