4.5 Article

A single residue in transmembrane domain 11 defines the different affinity for thiazides between the mammalian and flounder NaCl transporters

期刊

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
卷 299, 期 5, 页码 F1111-F1119

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajprenal.00412.2010

关键词

diuretics; distal convoluted tubule; salt transport

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [DK-64635]
  2. Mexican Council of Science and Technology [59992, 104451]

向作者/读者索取更多资源

Castaneda-Bueno M, Vazquez N, Bustos-Jaimes I, Hernandez D, Rodriguez-Lobato E, Pacheco-Alvarez D, Carino-Cortes R, Moreno E, Bobadilla NA, Gamba G. A single residue in transmembrane domain 11 defines the different affinity for thiazides between the mammalian and flounder NaCl transporters. Am J Physiol Endocrinol Metab 299: F1111-F1119, 2010. First published August 18, 2010; doi:10.1152/ajprenal.00412.2010.-Little is known about the residues that control the binding and affinity of thiazide-type diuretics for their protein target, the renal Na+-Cl- cotransporter (NCC). Previous studies from our group have shown that affinity for thiazides is higher in rat (rNCC) than in flounder (flNCC) and that the transmembrane region (TM) 8-12 contains the residues that produce this difference. Here, an alignment analysis of TM 8-12 revealed that there are only six nonconservative variations between flNCC and mammalian NCC. Two are located in TM9, three in TM11, and one in TM12. We used site-directed mutagenesis to generate rNCC containing flNCC residues, and thiazide affinity was assessed using Xenopus laevis oocytes. Wild-type or mutant NCC activity was measured using Na-22(+) uptake in the presence of increasing concentrations of metolazone. Mutations in TM11 conferred rNCC an flNCC-like affinity, which was caused mostly by the substitution of a single residue, S575C. Supporting this observation, the substitution C576S conferred to flNCC an rNCC-like affinity. Interestingly, the S575C mutation also rendered rNCC more active. Substitution of S575 in rNCC for other residues, such as alanine, aspartate, and lysine, did not alter metolazone affinity, suggesting that reduced affinity in flNCC is due specifically to the presence of a cysteine. We conclude that the difference in metolazone affinity between rat and flounder NCC is caused mainly by a single residue and that this position in the protein is important for determining its functional properties.

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