Effects of troponin I phosphorylation on conformational exchange in the regulatory domain of cardiac troponin C

J Biol Chem. 1999 Jun 11;274(24):16681-4. doi: 10.1074/jbc.274.24.16681.

Abstract

Conformational exchange has been demonstrated within the regulatory domain of calcium-saturated cardiac troponin C when bound to the NH2-terminal domain of cardiac troponin I-(1-80), and cardiac troponin I-(1-80)DD, having serine residues 23 and 24 mutated to aspartate to mimic the phosphorylated form of the protein. Binding of cardiac troponin I-(1-80) decreases conformational exchange for residues 29, 32, and 34. Comparison of average transverse cross correlation rates show that both the NH2- and COOH-terminal domains of cardiac troponin C tumble with similar correlation times when bound to cardiac troponin I-(1-80). In contrast, the NH2- and COOH-terminal domains in free cardiac troponin C and cardiac troponin C bound cardiac troponin I-(1-80)DD tumble independently. These results suggest that the nonphosphorylated cardiac specific NH2 terminus of cardiac troponin I interacts with the NH2-terminal domain of cardiac troponin C.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aspartic Acid / genetics
  • Computer Simulation
  • Mutation
  • Myocardium*
  • Nuclear Magnetic Resonance, Biomolecular
  • Phosphorylation
  • Protein Binding
  • Protein Conformation
  • Serine / genetics
  • Solutions
  • Troponin C / chemistry
  • Troponin C / metabolism*
  • Troponin I / metabolism*

Substances

  • Solutions
  • Troponin C
  • Troponin I
  • Aspartic Acid
  • Serine