Zinc inhibits calcineurin activity in vitro by competing with nickel

Biochem Biophys Res Commun. 2003 Jul 18;307(1):64-8. doi: 10.1016/s0006-291x(03)01122-7.

Abstract

Calcineurin (CN) is a Ca(2+)/calmodulin (CaM)-dependent protein serine/threonine phosphatase that contains Zn(2+) in its catalytic domain and can be stimulated by divalent ions such as Mn(2+) and Ni(2+). In this study, the role of exogenous Zn(2+) in the regulation of CN activity and its relevance to the role of Ni(2+) was investigated. Zn(2+) at a concentration range of 10nM-10 micro M inhibited Ni(2+)-stimulated CN-activity in vitro in a dose-dependent manner and approximately 50% inhibition was attained with 0.25 micro M Zn(2+). Kinetic analysis showed that Zn(2+) inhibited the activity of CN by competing with Ni(2+). Interaction of CN and CaM was not inhibited with Zn(2+) at 10 micro M. Zn(2+) never affected the activity of cAMP phosphodiesterase 1 or myosin light-chain kinase (CaM-dependent enzymes) and rather activated alkaline phosphatase. The present results indicate that Zn(2+) should be a potent inhibitor for CN activity although this ion is essential for CN.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Calcineurin / metabolism
  • Calcineurin Inhibitors*
  • Calmodulin / metabolism
  • Catalytic Domain
  • Cattle
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Myosin-Light-Chain Kinase / metabolism
  • Nickel / metabolism*
  • Phosphodiesterase I
  • Phosphoric Diester Hydrolases / metabolism
  • Zinc / metabolism*
  • Zinc / pharmacology

Substances

  • Calcineurin Inhibitors
  • Calmodulin
  • Nickel
  • Myosin-Light-Chain Kinase
  • Alkaline Phosphatase
  • Calcineurin
  • Phosphoric Diester Hydrolases
  • Phosphodiesterase I
  • Zinc