A Novel Topology Model of the Human Na+/H+ Exchanger Isoform 1

Shigeo Wakabayashi,Tianxiang Pang,Xiaohua Su,Munekazu Shigekawa

doi:10.1074/jbc.275.11.7942

Shigeo Wakabayashi, Tianxiang Pang + Show 2 more

Open Access

https://doi.org/10.1074/jbc.275.11.7942

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Abstract

The membrane topology of the human Na(+)/H(+) exchanger isoform 1 (NHE1) was assessed by substituted cysteine accessibility analysis. Eighty-three cysteine residues were individually introduced into a functional cysteineless NHE1, and these mutants were expressed in the exchanger-deficient PS120 cells. The topological disposition of introduced cysteines was determined by labeling with a biotinylated maleimide in the presence or absence of preincubation with the membrane-impermeable sulfhydryl reagent, 2-trimethylammoniumethyl-methanethiosulfonate in streptolysin O-permeabilized or nonpermeabilized cells. We proposed a new model for the topology of NHE1 that is significantly different from the model derived from hydropathy analysis. In this model, NHE1 is composed of 12 transmembrane segments (TMs) with the N and C termini located in the cytosol. The large, last extracellular loop in the membrane domain of the original model was suggested to comprise an intracellular loop, a new transmembrane segment (TM11), and an extracellular loop in the new model. Interestingly, cysteines at 183 and 184 and at 324 and 325 mapped to intracellular loops connecting TMs 4 and 5 (IL2) and TMs 8 and 9 (IL4), respectively, were accessible to sulfhydryl reagents from the outside. Furthermore, exchange activities of two mutants, R180C and Q181C, within IL2 were markedly inhibited by external MTSET. These data suggest that part of IL2 or IL4 may be located in a pore-lining region that is accessible from either side of the membrane and involved in ion transport.

Highlights

The Naϩ/Hϩ exchanger isoform 1 (NHE1),1 which catalyzes an electroneutral exchange of Naϩ for Hϩ across the plasma membrane, is involved in the regulation of intracellular pH and cell volume (1, 2)
Based on the detailed analysis, we proposed a new topology model of NHE1, which consists of 12-transmembrane segments with the N and C termini located in the cytosol
We have utilized the reactivity of introduced cysteines toward biotinylating reagent to determine the membrane topology of NHE1

Summary

Introduction

The Naϩ/Hϩ exchanger isoform 1 (NHE1),1 which catalyzes an electroneutral exchange of Naϩ for Hϩ across the plasma membrane, is involved in the regulation of intracellular pH (pHi) and cell volume (1, 2). The variable efficiency of biotinylation suggests that the first extracellular loop may form a structure in which some amino acid residues are not readily accessible to biotin maleimide.

Results

Conclusion