Conformational modulation of slow skeletal muscle troponin T by an NH(2)-terminal metal-binding extension

Am J Physiol Cell Physiol. 2000 Oct;279(4):C1067-77. doi: 10.1152/ajpcell.2000.279.4.C1067.

Abstract

Troponin T (TnT) is an essential element in the thin filament Ca(2+)-regulatory system controlling striated muscle contraction. Alternative RNA splicing generates developmental and muscle type-specific TnT isoforms differing in the hypervariable NH(2)-terminal region. Using avian fast skeletal muscle TnT containing a metal-binding segment, we have demonstrated a role of the NH(2)-terminal domain in modulating the conformation of TnT (Wang J and Jin JP. Biochemistry 37: 14519-14528, 1998). To further investigate the structure-function relationship of TnT, the present study constructed and characterized a recombinant protein in which the metal-binding peptide present in avian fast skeletal muscle TnT was fused to the NH(2) terminus of mouse slow skeletal muscle TnT. Metal ion or monoclonal antibody binding to the NH(2)-terminal extension induced conformational changes in other domains of the model TnT molecule. This was shown by the altered affinity to a monoclonal antibody against the COOH-terminal region and a polyclonal antiserum recognizing multiple epitopes. Protein binding assays showed that metal binding to the NH(2)-terminal extension had effects on the interaction of TnT with troponin I, troponin C, and most significantly, tropomyosin. The data indicate that the NH(2)-terminal Tx [4-7 repeats of a sequence motif His-(Glu/Ala)-Glu-Ala-His] extension confers a specific conformational modulation in the slow skeletal muscle TnT.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / metabolism
  • Calcium / metabolism
  • Cattle
  • Chickens
  • Enzyme-Linked Immunosorbent Assay
  • Epitopes / genetics
  • Epitopes / metabolism
  • Mice
  • Models, Molecular
  • Muscle Fibers, Fast-Twitch / metabolism*
  • Muscle Fibers, Slow-Twitch / metabolism*
  • Muscle, Skeletal / chemistry*
  • Protein Binding / genetics
  • Protein Conformation
  • Protein Structure, Tertiary / genetics
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Structure-Activity Relationship
  • Tropomyosin / metabolism
  • Troponin C / metabolism
  • Troponin I / metabolism
  • Troponin T / chemistry*
  • Troponin T / genetics
  • Troponin T / metabolism*
  • Zinc / metabolism*

Substances

  • Antibodies, Monoclonal
  • Epitopes
  • Recombinant Fusion Proteins
  • Tropomyosin
  • Troponin C
  • Troponin I
  • Troponin T
  • Zinc
  • Calcium