Inhibition of phosphate transport across the human erythrocyte membrane by chemical modification of sulfhydryl groups
- PMID: 1536838
- DOI: 10.1021/bi00122a010
Inhibition of phosphate transport across the human erythrocyte membrane by chemical modification of sulfhydryl groups
Abstract
Effects of sulfhydryl-reactive reagents on phosphate transport across human erythrocyte membranes were examined using 31P NMR. Phosphate transport was significantly inhibited in erythrocytes treated with sulfhydryl modifiers such as N-ethylmaleimide, diamide, and Cu2+/o-phenanthroline. Quantitation of sulfhydryl groups in band 3 showed that the inhibition is closely associated with the decrease of sulfhydryl groups. Data from erythrocytes treated with diamide or Cu2+/o-phenanthroline demonstrated that intermolecular cross-linking of band 3 by oxidation of a sulfhydryl group, perhaps Cys-201 or Cys-317, decreases the phosphate influx by about 10%. The inhibition was reversed by reduction using dithiothreitol. These results suggest that sulfhydryl groups in the cytoplasmic domain of band 3 may play an important role in the regulation of anion exchange across the membrane.
Similar articles
-
Role of sulfhydryl groups in band 3 in the inhibition of phosphate transport across erythrocyte membrane in visceral leishmaniasis.Arch Biochem Biophys. 2005 Apr 1;436(1):121-7. doi: 10.1016/j.abb.2005.01.015. Arch Biochem Biophys. 2005. PMID: 15752716
-
Reactive sulfhydryl groups of the band 3 polypeptide from human erythrocyte membranes. Identification of the sulfhydryl groups involved in Cu2+-o-phenanthroline cross-linking.J Biol Chem. 1979 Jul 10;254(13):6151-5. J Biol Chem. 1979. PMID: 447702 No abstract available.
-
Incorporation of 3H-N-ethylmaleimide into sheep red cell membrane thiol groups following protection by diamide-induced oxidation.Mol Cell Biochem. 1992 Sep 8;114(1-2):13-20. doi: 10.1007/BF00240292. Mol Cell Biochem. 1992. PMID: 1461256
-
Cross-linking of hemoglobin to the cytoplasmic surface of human erythrocyte membranes. Identification of band 3 as a site for hemoglobin binding in Cu2+-o-phenanthroline catalyzed cross-linking.J Biol Chem. 1981 Dec 25;256(24):13152-8. J Biol Chem. 1981. PMID: 7309756
-
The role of membrane sulfhydryls in passive, mediated transport processes and for the barrier function of the erythrocyte membrane.Membr Biochem. 1986;6(4):309-26. doi: 10.3109/09687688609065455. Membr Biochem. 1986. PMID: 3553858 Review. No abstract available.
Cited by
-
Se-mediated domain-domain communication in band 3 of human erythrocytes.Biol Trace Elem Res. 1996 Dec;55(3):279-95. doi: 10.1007/BF02785286. Biol Trace Elem Res. 1996. PMID: 9096855
-
Cell physiology and molecular mechanism of anion transport by erythrocyte band 3/AE1.Am J Physiol Cell Physiol. 2021 Dec 1;321(6):C1028-C1059. doi: 10.1152/ajpcell.00275.2021. Epub 2021 Oct 20. Am J Physiol Cell Physiol. 2021. PMID: 34669510 Free PMC article. Review.
-
Lysosomal sulphate transport is dependent upon sulphydryl groups.Biochem J. 1998 Mar 1;330 ( Pt 2)(Pt 2):713-7. doi: 10.1042/bj3300713. Biochem J. 1998. PMID: 9480880 Free PMC article.