CARP interacts with titin at a unique helical N2A sequence and at the domain Ig81 to form a structured complex

FEBS Lett. 2016 Sep;590(18):3098-110. doi: 10.1002/1873-3468.12362. Epub 2016 Sep 2.

Abstract

The cardiac ankyrin repeat protein (CARP) is up-regulated in the myocardium during cardiovascular disease and in response to mechanical or toxic stress. Stress-induced CARP interacts with the N2A spring region of the titin filament to modulate muscle compliance. We characterize the interaction between CARP and titin-N2A and show that the binding site in titin spans the dual domain UN2A-Ig81. We find that the unique sequence UN2A is not structurally disordered, but that it has a stable, elongated α-helical fold that possibly acts as a constant force spring. Our findings portray CARP/titin-N2A as a structured node and help to rationalize the molecular basis of CARP mechanosensing in the sarcomeric I-band.

Keywords: SEC-MALLS; X-ray crystallography; circular dichroism; recombinant proteins; small-angle X-ray scattering.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Connectin / chemistry
  • Connectin / metabolism*
  • Humans
  • Muscle Proteins / chemistry*
  • Muscle Proteins / metabolism
  • Nuclear Proteins / chemistry*
  • Nuclear Proteins / metabolism
  • Protein Binding
  • Protein Conformation, alpha-Helical
  • Repressor Proteins / chemistry*
  • Repressor Proteins / metabolism

Substances

  • ANKRD1 protein, human
  • Connectin
  • Muscle Proteins
  • Nuclear Proteins
  • Repressor Proteins