H+ and Cation Movements Associated with ADP, ATP Transport in Mitochondria

20Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

H+ and K+ movement associated with the mitochondrial ADP‐ATP exchange have been measured by glass electrode recordings in order to investigate the energy control of the ADP‐ATP exchange. All measurements are taken in the presence of oligomycin and inhibitors of electron transport in order to exclude other types of H+ transfer. ATP exchange against endogenous ADP as induced by addition of ATP gives only a small H+ uptake which is partially suppressed in a KCl medium. H+ uptake is increased strongly on addition of uncoupler. On addition of valinomycin, K+ is taken up instead of H+. With carbonylcyanide p‐trifluoromethoxyphenylhydrazone (FCCP) and valinomycin respectively, equivalent amounts of H+ and K+ are taken up over a wide range of protein and ATP concentration. The ATP dependence gives a ratio H+ per ATP added = 0.38 and K+ per ATP added = 0.27. Saturation with ATP is reached at about 14 μmol ATP/g protein for H+ uptake and 20 μmol ATP/g protein for K+ uptake. The FCCP‐facilitated, ATP‐induced H+ uptake increases with endogenous content of ADP, giving a ratio H+/ADP = 0.67. Kinetics of the H+ uptake and ATP‐induced nucleotide exchange are closely correlated to about 0.62 H+/nucleotide released. The temperature dependence of the H+ uptake rate measured between 4 and 11 °C gives an activation energy = 33 kcal (138 kJ), similar to that found for the exchange rate. In the exchange of ADP against endogenous ATP as started by addition of ADP, H+ are released in the absence of FCCP. In the presence of FCCP, H+ release is only marked when endogenous nucleotides are preloaded with external ATP. This H+ release is decreased by Pi and enhanced by N‐ethylmaleimide, blocking Pi transfer. It varies according to endogenous ATP content reaching the ratio H+ released/endogenous ATP = 0.3 to 0.5. These data have been interpreted to indicate that the ATPe‐ADPi exchange is largely electrical and the opposite ADPe‐ATPi exchange is only between 50 to 70% electrical. The implications for energy transfer are discussed. Copyright © 1978, Wiley Blackwell. All rights reserved

References Powered by Scopus

Chemiosmotic coupling in oxidative and photosynthetic phosphorylation.

1819Citations
N/AReaders
Get full text

The Influence of Respiration and ATP Hydrolysis on the Proton‐Electrochemical Gradient across the Inner Membrane of Rat‐Liver Mitochondria as Determined by Ion Distribution

506Citations
N/AReaders
Get full text

Estimation of Membrane Potential and pH Difference across the Cristae Membrane of Rat Liver Mitochondria

415Citations
N/AReaders
Get full text

Cited by Powered by Scopus

The ADP and ATP transport in mitochondria and its carrier

515Citations
N/AReaders
Get full text

Regulation of cellular energy metabolism

339Citations
N/AReaders
Get full text

Compartmentation and Communication in Living Systems. Ligand Conduction: a General Catalytic Principle in Chemical, Osmotic and Chemiosmotic Reaction Systems

249Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

WULF, R., KALTSTEIN, A., & KLINGENBERG, M. (1978). H+ and Cation Movements Associated with ADP, ATP Transport in Mitochondria. European Journal of Biochemistry, 82(2), 585–592. https://doi.org/10.1111/j.1432-1033.1978.tb12054.x

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 6

46%

Professor / Associate Prof. 4

31%

Researcher 3

23%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 6

50%

Biochemistry, Genetics and Molecular Bi... 4

33%

Chemistry 1

8%

Physics and Astronomy 1

8%

Save time finding and organizing research with Mendeley

Sign up for free