Evaluation of alternatives to warfarin as probes for Sudlow site I of human serum albumin Characterization by high-performance affinity chromatography

摘要

Warfarin is often used as a site-specific probe for examining the binding of drugs and other solutes to sudlow site I of human serum albumin (HSA). However, warfarin has strong binding to HSА and the two chiral forms of warfarin have slightly different binding affinities for this protein. Warfarin also under_goes a slow change in structure when present in common buffers used for binding studies. This report examined the use of four related, achiral compounds (i.e., coumarin, 7-hydroxycoumarin, 7-hydroxy_4-methylcoumarin, and 4-hydroxycoumarin) as possible alternative probes for Sudlow site 1 in drug binding studies. High-performance affinity chromatography and immobilized HSA columns were used to compare and evaluate the binding properties of these probe candidates. Binding for each of the tested probe candidates to HSA was found to give a good fit to a two-site model. The first group of sites had moderate-to-high affinities for the probe candidates with association equilibrium constants that ranged from 6.4 × 10~3 M~-1 (coumarin) to 5.5 × 10~4 M~-1 (4-hydroxycoumarin) at pH 7.4 and 37 _С. The second group of weaker, and probably non-specific, binding regions, had association equilibrium constants that ranged from3.8 × 10~1 M~-1 (7-hydroxy-4-methylcoumarin)to7.3 × 10~2 M~-1 (coumarin).Competitionexperiments based on zonal elution indicated that all of these probe candidates competed with warfarin at their high affinity regions. Warfarin also showed competition with coumarin, 7-hydroxycoumarin and 7-hydroxy_4-methycoumarin for their weak affinity sites but appeared to not bind and/or compete for all of the weak sites of 4-hydroxycoumarin. It was found from this group that 4-hydroxycoumarin was the best alternative to warfarin for examining the interactions of drugs at sudlow site Ion HSA. These results also provided information on how the major structural components of warfarin contribute to the binding of this drug at sudlow site I.