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Studies of the regulatory mechanism of Ca2+/calmodulin-dependent protein kinase II. Mutation of threonine 286 to alanine and aspartate.

Publication ,  Journal Article
Fong, YL; Taylor, WL; Means, AR; Soderling, TR
Published in: J Biol Chem
October 5, 1989

A cDNA clone for the alpha subunit of mouse brain Ca2+/CaM-dependent protein kinase II (CaM-kinase II) was transcribed in vitro and translated in a rabbit reticulocyte lysate system. Inclusion of [35S]methionine in the translation system yielded a single 35S-polypeptide of about 50 kDa. When the translation system was assayed for CaM-kinase II activity, there was a 5-10-fold enrichment of kinase activity which was totally dependent on Ca2+/calmodulin (CaM). Both the 50-kDa 35S-polypeptide and the Ca2+/CaM-dependent protein kinase activity were quantitatively immunoprecipitated by rat brain CaM-kinase II antibody. When the translated wild-type kinase was subjected to autophosphorylation conditions in the presence of Ca2+, CaM, Mg2+, and ATP, the Ca2+-independent activity (assayed in the presence of [ethylenebis(oxyethylenenitrilo)]tetraacetic acid) increased from 5.8 +/- 0.7 to 26.5 +/- 2.1% of total activity (assayed in the presence of Ca2+/CaM). These properties confirm the identity of the kinase translated in vitro as CaM-kinase II. The role of Thr-286 autophosphorylation in formation of the Ca2+-independent activity was investigated by site-directed mutation of Thr-286 to Ala (Ala-286 kinase) and to Asp (Asp-286 kinase). The Ala-286 kinase was completely dependent on Ca2+/CaM for activity prior and subsequent to autophosphorylation. The Asp-286 kinase exhibited 21.9 +/- 0.8% Ca2+-independent activity, and this was not increased by autophosphorylation. These results establish that introduction of negative charge(s) at residue 286, either by autophosphorylation of Thr or by mutation to Asp, is sufficient and necessary to generate the partially Ca2+-independent form of CaM-kinase II.

Duke Scholars

Published In

J Biol Chem

ISSN

0021-9258

Publication Date

October 5, 1989

Volume

264

Issue

28

Start / End Page

16759 / 16763

Location

United States

Related Subject Headings

  • Transcription, Genetic
  • Threonine
  • Reticulocytes
  • Rats
  • Rabbits
  • Protein Kinases
  • Protein Biosynthesis
  • Plasmids
  • Oligonucleotide Probes
  • Mutation
 

Citation

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MLA
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Fong, Y. L., Taylor, W. L., Means, A. R., & Soderling, T. R. (1989). Studies of the regulatory mechanism of Ca2+/calmodulin-dependent protein kinase II. Mutation of threonine 286 to alanine and aspartate. J Biol Chem, 264(28), 16759–16763.
Fong, Y. L., W. L. Taylor, A. R. Means, and T. R. Soderling. “Studies of the regulatory mechanism of Ca2+/calmodulin-dependent protein kinase II. Mutation of threonine 286 to alanine and aspartate.J Biol Chem 264, no. 28 (October 5, 1989): 16759–63.
Fong YL, Taylor WL, Means AR, Soderling TR. Studies of the regulatory mechanism of Ca2+/calmodulin-dependent protein kinase II. Mutation of threonine 286 to alanine and aspartate. J Biol Chem. 1989 Oct 5;264(28):16759–16763.

Published In

J Biol Chem

ISSN

0021-9258

Publication Date

October 5, 1989

Volume

264

Issue

28

Start / End Page

16759 / 16763

Location

United States

Related Subject Headings

  • Transcription, Genetic
  • Threonine
  • Reticulocytes
  • Rats
  • Rabbits
  • Protein Kinases
  • Protein Biosynthesis
  • Plasmids
  • Oligonucleotide Probes
  • Mutation