Mapping the tropomyosin isoform 5 binding site on human erythrocyte tropomodulin: further insights into E-Tmod/TM5 interaction

Arch Biochem Biophys. 2005 Dec 15;444(2):130-8. doi: 10.1016/j.abb.2005.10.002. Epub 2005 Oct 27.

Abstract

Actin protofilaments in the erythrocyte membrane skeleton are uniformly approximately 37nm. This length may be in part attributed to a "molecular ruler" made of erythrocyte tropomodulin (E-Tmod) and tropomyosin (TM) isoforms 5 or 5b. We previously mapped the E-Tmod binding site to TM5 N-terminal heptad repeat residues "a" (I(7), I(14)), "d" (V(10)) and "f" (R(12)). We now map the TM5 binding site to E-Tmod residues at L(116), E(117) and/or E(118) by identifying among 35 deletion clones and a series of point mutations that no longer bind to human TM5 and rat TM5b. Upstream residues 71-104 contain an actin binding site. The N-terminal "KRK ring" may participate in balancing electrostatic force with hydrophobic interaction in dimerization of TM and its binding to E-Tmod.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Binding Sites
  • Computer Simulation
  • Humans
  • Models, Chemical*
  • Models, Molecular*
  • Molecular Sequence Data
  • Protein Binding
  • Protein Conformation
  • Protein Interaction Mapping
  • Tropomodulin / analysis
  • Tropomodulin / chemistry*
  • Tropomodulin / genetics
  • Tropomyosin / analysis
  • Tropomyosin / chemistry*
  • Tropomyosin / genetics

Substances

  • TMOD1 protein, human
  • TPM3 protein, human
  • Tropomodulin
  • Tropomyosin