CHARACTERIZATION OF BINDING-SITE OF UREMIC TOXINS ON HUMAN SERUM-ALBUMIN
Citation
T. Sakai et al., CHARACTERIZATION OF BINDING-SITE OF UREMIC TOXINS ON HUMAN SERUM-ALBUMIN, Biological & pharmaceutical bulletin, 18(12), 1995, pp. 1755-1761
Categorie Soggetti
Pharmacology & Pharmacy
SICI code
0918-6158(1995)18:12<1755:COBOUT>2.0.ZU;2-T
Abstract
The interaction of uremic toxins including indole-3-acetic acid (IA),
indoxyl sulfate (IS), hippuric acid (HA) and 3-carboxy-4-methyl-5-prop
yl-2-furanpropanoic acid (CMPF) with human serum albumin (HSA) has bee
n investigated by three methods of fluorescent probe displacement, ult
rafiltration and equilibrium dialysis. The binding parameter of CMPF w
as found to have the strongest affinity (10(7) M(-1)) among all the ur
emic toxins studied. Competitive experiment based on the method of Kra
gh-Hansen suggested that IA, IS and HA bind to site II, whereas CMPF b
inds to site I. The present limited data indicated that the four uremi
c toxins caused inhibition to any endo- or exogenous substances on HSA
.