4.5 Article

The Cardiac Ca2+-Sensitive Regulatory Switch, a System in Dynamic Equilibrium

Journal

BIOPHYSICAL JOURNAL
Volume 95, Issue 10, Pages 4772-4789

Publisher

CELL PRESS
DOI: 10.1529/biophysj.108.131318

Keywords

-

Categories

Funding

  1. National Institutes of Health [HL052508, HL80186]
  2. European Union [MSCF-CT-2004-013119]
  3. American Heart Association [0330170N]

Ask authors/readers for more resources

The Ca2+-sensitive regulatory switch of cardiac muscle is a paradigmatic example of protein assemblies that communicate ligand binding through allosteric change. The switch is a dimeric complex of troponin C (TnC), an allosteric sensor for Ca2+, and troponin I (TnI), an allosteric reporter. Time-resolved equilibrium Forster resonance energy transfer ( FRET) measurements suggest that the switch activates in two steps: a TnI-independent Ca2+-priming step followed by TnI-dependent opening. To resolve the mechanistic role of TnI in activation we performed stopped-flow FRET measurements of activation after rapid addition of a lacking component (Ca2+ or TnI) and deactivation after rapid chelation of Ca2+. Time-resolved measurements, stopped-flow measurements, and Ca2+-titration measurements were globally analyzed in terms of a new quantitative dynamic model of TnC-TnI allostery. The analysis provided a mesoscopic parameterization of distance changes, free energy changes, and transition rates among the accessible coarse-grained states of the system. The results reveal that 1), the Ca2+-induced priming step, which precedes opening, is the rate-limiting step in activation; 2), closing is the rate-limiting step in de-activation; 3), TnI induces opening; 4), there is an incompletely deactivated population when regulatory Ca2+ is not bound, which generates an accessory pathway of activation; and 5), there is incomplete activation by Ca2+-when regulatory Ca2+ is bound, a 3: 2 mixture of dynamically interconverting open ( active) and primed-closed ( partially active) conformers is observed (15 degrees C). Temperature-dependent stopped-flow FRET experiments provide a near complete thermokinetic parameterization of opening: the enthalpy change(Delta H=-33.4 kJ/mol), entropy change(Delta S= -0.110 kJ/mol/K), heat capacity change (Delta Cp=-7.6 kJ/mol/K), the enthalpy of activation (delta(double dagger) 10.6 kJ/mol) and the effective barrier crossing attempt frequency (nu(adj) = 1.8 x 10(4) s(-1)).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available