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Sites of interaction between kinase-related protein and smooth muscle myosin.

Publication ,  Journal Article
Silver, DL; Vorotnikov, AV; Watterson, DM; Shirinsky, VP; Sellers, JR
Published in: J Biol Chem
October 3, 1997

Kinase-related protein, also known as KRP or telokin, is an independently expressed protein product derived from a gene within the gene for myosin light chain kinase (MLCK). KRP binds to unphosphorylated smooth muscle myosin filaments and stabilizes them against ATP-induced depolymerization in vitro. KRP competes with MLCK for binding to myosin, suggesting that both proteins bind to myosin by the KRP domain (Shirinsky, V. P., Vorotnikov, A. V., Birukov, K. G., Nanaev, A. K., Collinge, M., Lukas, T. J., Sellers, J. R., and Watterson, D. M. (1993) J. Biol. Chem. 268, 16578-16583). In this study, we investigated which regions of myosin and KRP interact in vitro. Using cosedimentation assays, we determined that KRP binds to unphosphorylated myosin with a stoichiometry of 1 mol of KRP/1 mol of myosin and an affinity of 5.5 microM. KRP slows the rate of proteolytic cleavage of the head-tail junction of heavy meromyosin by papain and chymotrypsin, suggesting it is binding to this region of myosin. In addition, competition experiments, using soluble headless fragments of nonmuscle myosin, confirmed that KRP interacts with the regulatory light chain binding region of myosin. The regions important for KRP's binding to myosin were investigated using bacterially expressed KRP truncation mutants. We determined that the acid-rich sequence between Gly138 and Asp151 of KRP is required for high affinity myosin binding, and that the amino terminus and beta-barrel regions weakly interact with myosin. All KRP truncations, at concentrations comparable to their KD values, exhibited some stabilization of myosin filaments against ATP depolymerization in vitro, suggesting that KRP's ability to stabilize myosin filaments is commensurate with its myosin binding affinity. KRP weakened the Km but not the Vmax of phosphorylation of myosin by MLCK, demonstrating that bound KRP does not prevent MLCK from activating myosin.

Duke Scholars

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

October 3, 1997

Volume

272

Issue

40

Start / End Page

25353 / 25359

Location

United States

Related Subject Headings

  • Turkeys
  • Sequence Deletion
  • Recombinant Proteins
  • Protein Structure, Secondary
  • Polymerase Chain Reaction
  • Myosins
  • Mutagenesis, Site-Directed
  • Muscle, Smooth
  • Muscle Proteins
  • Molecular Sequence Data
 

Citation

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Silver, D. L., Vorotnikov, A. V., Watterson, D. M., Shirinsky, V. P., & Sellers, J. R. (1997). Sites of interaction between kinase-related protein and smooth muscle myosin. J Biol Chem, 272(40), 25353–25359. https://doi.org/10.1074/jbc.272.40.25353
Silver, D. L., A. V. Vorotnikov, D. M. Watterson, V. P. Shirinsky, and J. R. Sellers. “Sites of interaction between kinase-related protein and smooth muscle myosin.J Biol Chem 272, no. 40 (October 3, 1997): 25353–59. https://doi.org/10.1074/jbc.272.40.25353.
Silver DL, Vorotnikov AV, Watterson DM, Shirinsky VP, Sellers JR. Sites of interaction between kinase-related protein and smooth muscle myosin. J Biol Chem. 1997 Oct 3;272(40):25353–9.
Silver, D. L., et al. “Sites of interaction between kinase-related protein and smooth muscle myosin.J Biol Chem, vol. 272, no. 40, Oct. 1997, pp. 25353–59. Pubmed, doi:10.1074/jbc.272.40.25353.
Silver DL, Vorotnikov AV, Watterson DM, Shirinsky VP, Sellers JR. Sites of interaction between kinase-related protein and smooth muscle myosin. J Biol Chem. 1997 Oct 3;272(40):25353–25359.

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

October 3, 1997

Volume

272

Issue

40

Start / End Page

25353 / 25359

Location

United States

Related Subject Headings

  • Turkeys
  • Sequence Deletion
  • Recombinant Proteins
  • Protein Structure, Secondary
  • Polymerase Chain Reaction
  • Myosins
  • Mutagenesis, Site-Directed
  • Muscle, Smooth
  • Muscle Proteins
  • Molecular Sequence Data