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A sodium/proton antiporter in chromaffin-granule membranes
- Source :
- Biochemical Journal. 257:499-507
- Publication Year :
- 1989
- Publisher :
- Portland Press Ltd., 1989.
-
Abstract
- Chromaffin granules, the secretory vesicles of the adrenal medulla, have a Na+/H+ exchange activity in their membranes which brings their proton gradient into equilibrium with a Na+ gradient. This explains why Na+ is mildly inhibitory to amine transport (which is driven by the H+ gradient) The activity can be demonstrated by using accumulation of 22Na+ in response to a pH gradient that is either imposed by diluting membrane ‘ghosts’ into alkaline media, or generated by ATP hydrolysis. It can also be monitored indirectly by fluorescence measurements in which the pH inside ‘ghost’ is monitored by quenching of a fluorescent weak base. This method has been used to monitor Na+ entry into acid-loaded Șghosts’ of H+ entry into methylamine accumulation. The exchanger appears to be reversible and non-electrogenic, with a stoichiometry of 1:1. Using an indirect assay we measured an apparent Km for Na+ of 4.7 mM, and a Ki for amiloride, a competitive inhibitor, of 0.26 mM. Direct assays using 22Na+ suggested a higher Km. Ethylisopropylamiloride was not inhibitory.
- Subjects :
- Serotonin
Sodium
Fluorescence spectrometry
chemistry.chemical_element
Biochemistry
Antiporters
Membrane Potentials
Amine transport
chemistry.chemical_compound
Adenosine Triphosphate
Animals
Chromaffin Granules
Electrochemical gradient
Molecular Biology
Fluorescent Dyes
Chromatography
Aminoacridines
Chemistry
Methylamine
Cell Biology
Hydrogen-Ion Concentration
Membrane transport
Adrenal Medulla
Chromaffin System
Sodium-proton antiporter
Biophysics
Cattle
Protons
Carrier Proteins
Weak base
Research Article
Subjects
Details
- ISSN :
- 14708728 and 02646021
- Volume :
- 257
- Database :
- OpenAIRE
- Journal :
- Biochemical Journal
- Accession number :
- edsair.doi.dedup.....34a44f7c2db2da1b09c0ba3192074594
- Full Text :
- https://doi.org/10.1042/bj2570499