Literature DB >> 2848830

Mechanism of cis- and trans-substrate interactions at the tetraethylammonium/H+ exchanger of rabbit renal brush-border membrane vesicles.

S H Wright1, T M Wunz.   

Abstract

The kinetic basis for trans-effects of intravesicular substrates on the uptake of the organic cation, tetraethylammonium (TEA), into rabbit renal brush-border membrane vesicles (BBMV) was studied. Preloading BBMV with 1, 2, or 4 mM TEA stimulated the initial rate of uptake and the total net accumulation of 0.1 mM [3H]TEA. The stimulatory effect of intravesicular TEA on the initial rate of uptake was a saturable function of the trans-TEA concentration, with a half-maximal effect noted at an intravesicular concentration of 0.28 mM. A 1 mM trans-concentration of TEA increased the Jmax of [3H]TEA uptake (from 4.3 to 6.8 nmol.mg-1.min-1) without affecting the apparent Kt. An outwardly directed H+ gradient also increased Jmax (to 10.7 nmol.mg-1.min-1), although the addition of an outwardly directed TEA gradient did not produce further increases in the rate of TEA uptake. External H+ acted as a competitive inhibitor of TEA uptake, and an increase in external [H+] (from 32 nM to 100 nM) produced an increase in the apparent Kt for TEA transport (from 0.12 to 0.26 mM) without affecting the Jmax. The results suggested that TEA and H+ compete for a common site or set of mutually exclusive sites on the cytoplasmic and luminal aspects of TEA/H+ exchanger in the renal brush border, and that these sites have a similar affinity for TEA.

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Year:  1988        PMID: 2848830

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  10 in total

1.  Twelve transmembrane helices form the functional core of mammalian MATE1 (multidrug and toxin extruder 1) protein.

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2.  Kinetic analysis of tetraethylammonium transport in the kidney epithelial cell line, LLC-PK1.

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3.  A choline transporter in renal brush-border membrane vesicles: energetics and structural specificity.

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4.  Interaction of H+ with the extracellular and intracellular aspects of hMATE1.

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5.  Unstirred Water Layers and the Kinetics of Organic Cation Transport.

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6.  Characterization of guanidine transport in human renal brush border membranes.

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7.  Electroneutral, HCO3(-)-independent, pH gradient-dependent uphill transport of Cl- by ileal brush-border membrane vesicles. Possible role in the pathogenesis of chloridorrhea.

Authors:  M Vasseur; M Caüzac; F Alvarado
Journal:  Biochem J       Date:  1989-11-01       Impact factor: 3.857

8.  Structure and interaction of inhibitors with the TEA/H+ exchanger of rabbit renal brush border membranes.

Authors:  S H Wright; T M Wunz; T P Wunz
Journal:  Pflugers Arch       Date:  1995-01       Impact factor: 3.657

9.  The multidrug transporter MATE1 sequesters OCs within an intracellular compartment that has no influence on OC secretion in renal proximal tubules.

Authors:  L J Martínez-Guerrero; K K Evans; W H Dantzler; S H Wright
Journal:  Am J Physiol Renal Physiol       Date:  2015-11-04

10.  Transport Turnover Rates for Human OCT2 and MATE1 Expressed in Chinese Hamster Ovary Cells.

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Journal:  Int J Mol Sci       Date:  2022-01-27       Impact factor: 6.208

  10 in total

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