Sarcoplasmic reticulum calcium ATPase. Labeling of a putative Mg2+ site by reaction with a carbodiimide and a spin-label

FEBS Lett. 1993 Nov 29;335(1):33-6. doi: 10.1016/0014-5793(93)80433-u.

Abstract

The sarcoplasmic reticulum Ca(2+)-ATPase loses hydrolytic activity and the ability to be phosphorylated by Pi following incubation with EDC [1-ethyl-3-(3-dimethylaminopropyl)carbodiimide]. 4 nmol of tempamine per mg SR protein can be coupled to either a glu or an asp side chain through the EDC reaction. Mg2+ protects against loss of activity and tempamine labeling with a mid-point of about 3 mM in the absence of Ca2+. This is similar to the Kd for a Mg2+ that serves as a cofactor in enzyme phosphorylation. The Mg2+ protection constant is lowered by an order of magnitude when Ca2+ is bound to the transport sites. It is suggested that control of the Mg2+ binding site affinity may be part of the mechanism of enzyme activation by Ca2+.

MeSH terms

  • Animals
  • Aspartic Acid / metabolism
  • Binding Sites
  • Calcium / pharmacology
  • Calcium-Transporting ATPases / antagonists & inhibitors
  • Calcium-Transporting ATPases / metabolism*
  • Cyclic N-Oxides / metabolism*
  • Egtazic Acid / pharmacology
  • Ethyldimethylaminopropyl Carbodiimide / metabolism*
  • Ethyldimethylaminopropyl Carbodiimide / pharmacology
  • Glutamates / metabolism
  • Glutamic Acid
  • Kinetics
  • Magnesium / metabolism*
  • Magnesium / pharmacology
  • Muscles / enzymology*
  • Phosphorylation
  • Rabbits
  • Sarcoplasmic Reticulum / enzymology*
  • Spin Labels*

Substances

  • Cyclic N-Oxides
  • Glutamates
  • Spin Labels
  • 4-amino-TEMPO
  • Aspartic Acid
  • Glutamic Acid
  • Egtazic Acid
  • Calcium-Transporting ATPases
  • Magnesium
  • Ethyldimethylaminopropyl Carbodiimide
  • Calcium