4-aminomethylbenzoic acid is a non-translocated competitive inhibitor of the epithelial peptide transporter PepT1

被引:45
作者
Meredith, D
Boyd, CAR
Bronk, JR
Bailey, PD
Morgan, KM
Collier, ID
Temple, CS
机构
[1] Univ Oxford, Dept Human Anat, Oxford OX1 3QX, England
[2] Univ York, Dept Biol, York YO1 5DD, N Yorkshire, England
[3] Heriot Watt Univ, Dept Chem, Edinburgh EH14 4AS, Midlothian, Scotland
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1998年 / 512卷 / 03期
基金
英国惠康基金;
关键词
D O I
10.1111/j.1469-7793.1998.629bd.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. 4-Aminomethylbenzoic acid, a molecule which mimics the spatial configuration of a dipeptide, competitively inhibits peptide influx in both Xenopus laevis oocytes expressing rabbit PepT1 and through PepT1 in rat renal brush border membrane vesicles. 2. This molecule is not translocated through PepT1 as measured both by direct HPLC analysis in PepT1-expressing oocytes and indirectly by its failure to trans-stimulate labelled peptide efflux through PepT1 in oocytes and in renal membrane vesicles. 3. However 4-aminomethylbenzoic acid does reverse trans-stimulation through expressed PepT1 of labelled peptide efflux induced by unlablled peptide. Quantitatively this reversal is compatible with 4-aminomethylbenzoic acid competitively binding to the external surface of PepT1. 4. 4-Aminomethylbenzoic acid (the first molecule discovered to be a non-translocated competitive inhibitor of proton-coupled oligopeptide transport) and its derivatives may thus be particularly useful as experimental tools.
引用
收藏
页码:629 / 634
页数:6
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