Inaba M, Goto I, Sato K, Maede Y
Department of Veterinary Internal Medicine, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
J Vet Med Sci. 1993 Apr;55(2):281-5. doi: 10.1292/jvms.55.281.
This report describes a unique response of the anion transporter in equine erythrocytes to the fluorescent substrate N-(2-aminoethyl sulfonate)-7-nitrobenz-2-oxa-3-diazole (NBD-taurine). Equine erythrocytes showed fluxes of NBD-taurine both inward and outward at rates considerably slower than those in human cells. These fluxes were completely abolished by a typical anion transport inhibitor, 4,4'-diisothiocyanostilbene-2,2'-disulfonate. Furthermore, NBD-taurine competitively inhibited the uptake of phosphate in equine red cells with an inhibition constant of phosphate that was slightly higher than the Michaelis constant of phosphate uptake. These results demonstrate that the anion transporter (band 3) in equine red cells binds NBD-taurine but does not prefer it as the substrate for transport, suggesting a structural difference between equine and human anion transporters at the polypeptide portion which is implicated in anion transport.
本报告描述了马红细胞中阴离子转运体对荧光底物N-(2-氨基乙基磺酸盐)-7-硝基苯并-2-恶唑-3-二氮杂萘(NBD-牛磺酸)的独特反应。马红细胞显示出NBD-牛磺酸的内流和外流通量,其速率比人类细胞中的通量慢得多。这些通量被典型的阴离子转运抑制剂4,4'-二异硫氰基芪-2,2'-二磺酸盐完全消除。此外,NBD-牛磺酸竞争性抑制马红细胞对磷酸盐的摄取,其对磷酸盐的抑制常数略高于磷酸盐摄取的米氏常数。这些结果表明,马红细胞中的阴离子转运体(带3)与NBD-牛磺酸结合,但不将其作为运输的首选底物,这表明马和人类阴离子转运体在涉及阴离子运输的多肽部分存在结构差异。