The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles

The kinetics and the stoichiometry of the Ca²⁺ pump in human erythrocytes was investigated using inside-out vesicles as a model. Inside-out vesicles were prepared by a modified procedure of Steck and Kant (12) outlined by Quist and Roufogalis(9), Since calmodulin has been shown to regulate the activ...

Full description

Bibliographic Details
Main Author: Akyempon, Christian Kweku
Language:English
Published: 2010
Online Access:http://hdl.handle.net/2429/22849
id ndltd-UBC-oai-circle.library.ubc.ca-2429-22849
record_format oai_dc
spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-228492018-01-05T17:41:52Z The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles Akyempon, Christian Kweku The kinetics and the stoichiometry of the Ca²⁺ pump in human erythrocytes was investigated using inside-out vesicles as a model. Inside-out vesicles were prepared by a modified procedure of Steck and Kant (12) outlined by Quist and Roufogalis(9), Since calmodulin has been shown to regulate the activites of the (Ca²⁺ + Mg²⁺)-ATPase, and the Ca²⁺ transport system (49, 50), its effect on the kinetics and stoichiometry was also investigated in inside-out vesicles treated with EDTA to remove endogeneous calmodulin (78). The calmodulin used in this study was purified from human erythrocytes. The stoichiometry of the Ca²⁺ pump was found to vary with intracellular Ca²⁺ concentration: in a low Ca²⁺ concentration range of 0.71 μM to 24 μM, it was estimated to be close to 2 whereas in the high Ca²⁺ range -50 μM to 300 μM, it was estimated to be close to 1. Calmodulin, ATP concentrations from 0.1 - 3 mM and Mg²⁺ concentrations of 3 mM and above did not alter the stoichiometry while a stoichiometry of 2 was obtained at 1 mM Mg²⁺ concentration at all Ca²⁺ concentrations studied. A model for Ca²⁺ efflux is suggested to explain these results. Calmodulin was found to increase the V[sub max] and the affinity of the (Ca²⁺+ Mg²⁺)-ATPase for Ca²⁺. The high affinity component was found to have a K[sub diss] (K[sub l]) of 2 to 4 μM Ca²⁺ whereas the low Ca²⁺ affinity component was found to have a K[sub diss] of 200 t0 300 μM Ca²⁺ Lowering Mg²⁺concentrations in the presence of calmodulin resulted in the predominance of the high affinity component of the Ca²⁺ - transport system which was inhibited at high Ca²⁺ concentrations. Competition between Ca²⁺ and Mg²⁺ for an inhibitory site located on the high affinity form, E[sub l]P of (Ca²⁺ + Mg²⁺ )-ATPase enzyme is suggested to account for the Ca²⁺ inhibition observed at low Mg²⁺ concentrations. Pharmaceutical Sciences, Faculty of Graduate 2010-03-29T17:25:10Z 2010-03-29T17:25:10Z 1981 Text Thesis/Dissertation http://hdl.handle.net/2429/22849 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.
collection NDLTD
language English
sources NDLTD
description The kinetics and the stoichiometry of the Ca²⁺ pump in human erythrocytes was investigated using inside-out vesicles as a model. Inside-out vesicles were prepared by a modified procedure of Steck and Kant (12) outlined by Quist and Roufogalis(9), Since calmodulin has been shown to regulate the activites of the (Ca²⁺ + Mg²⁺)-ATPase, and the Ca²⁺ transport system (49, 50), its effect on the kinetics and stoichiometry was also investigated in inside-out vesicles treated with EDTA to remove endogeneous calmodulin (78). The calmodulin used in this study was purified from human erythrocytes. The stoichiometry of the Ca²⁺ pump was found to vary with intracellular Ca²⁺ concentration: in a low Ca²⁺ concentration range of 0.71 μM to 24 μM, it was estimated to be close to 2 whereas in the high Ca²⁺ range -50 μM to 300 μM, it was estimated to be close to 1. Calmodulin, ATP concentrations from 0.1 - 3 mM and Mg²⁺ concentrations of 3 mM and above did not alter the stoichiometry while a stoichiometry of 2 was obtained at 1 mM Mg²⁺ concentration at all Ca²⁺ concentrations studied. A model for Ca²⁺ efflux is suggested to explain these results. Calmodulin was found to increase the V[sub max] and the affinity of the (Ca²⁺+ Mg²⁺)-ATPase for Ca²⁺. The high affinity component was found to have a K[sub diss] (K[sub l]) of 2 to 4 μM Ca²⁺ whereas the low Ca²⁺ affinity component was found to have a K[sub diss] of 200 t0 300 μM Ca²⁺ Lowering Mg²⁺concentrations in the presence of calmodulin resulted in the predominance of the high affinity component of the Ca²⁺ - transport system which was inhibited at high Ca²⁺ concentrations. Competition between Ca²⁺ and Mg²⁺ for an inhibitory site located on the high affinity form, E[sub l]P of (Ca²⁺ + Mg²⁺ )-ATPase enzyme is suggested to account for the Ca²⁺ inhibition observed at low Mg²⁺ concentrations. === Pharmaceutical Sciences, Faculty of === Graduate
author Akyempon, Christian Kweku
spellingShingle Akyempon, Christian Kweku
The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles
author_facet Akyempon, Christian Kweku
author_sort Akyempon, Christian Kweku
title The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles
title_short The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles
title_full The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles
title_fullStr The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles
title_full_unstemmed The kinetics of Ca²⁺ transport and (Ca²⁺ + Mg²⁺)-ATPase activity in human erythrocyte inside-out vesicles
title_sort kinetics of ca²⁺ transport and (ca²⁺ + mg²⁺)-atpase activity in human erythrocyte inside-out vesicles
publishDate 2010
url http://hdl.handle.net/2429/22849
work_keys_str_mv AT akyemponchristiankweku thekineticsofca2transportandca2mg2atpaseactivityinhumanerythrocyteinsideoutvesicles
AT akyemponchristiankweku kineticsofca2transportandca2mg2atpaseactivityinhumanerythrocyteinsideoutvesicles
_version_ 1718592142968881152