eLifePhysiologyPeer-reviewed journal article
Probing relaxed myosin states in hypertrophic cardiomyopathy by second harmonic-generation microscopy
Giulia ArecchiiD, Marica DenteiD, Weikang MaiD, Beatrice ScelliniiD, Nicoletta PiroddiiD, Marina ScardigliiD, Jingyuan YuiD, Jing ZhaoiD, Riccardo CicchiiD, Ryo KinegawaiD, Caroline Muellenbroich, Francesco SeraiD, Corrado PoggesiiD, Cecilia FerrantiniiD, Thomas C. IrvingiD, Michael RegnieriD, Leonardo SacconiiD, Chiara TesiiD
Abstract
This study explores the use of polarized second-harmonic generation (pSHG) to investigate myosin conformation in the relaxed state, differentiating between the actin-available, disordered (ON) state and the energy-conserving, ordered (OFF) state. By shifting the ON/OFF equilibrium using both physical and chemical manipulations, we demonstrate the sensitivity of pSHG in quantifying the ON/OFF ratio in skeletal and cardiac tissues. Comparisons with X-ray diffraction measurements further validate our findings. Applying this approach to a sarcomeric mutation associated with hypertrophic cardiomyopathy, we show that R403Q/MYH7-mutated minipig ventricle tissue exhibits a higher ON fraction compared to controls. This difference is abolished under high concentrations of a myosin activator (2-deoxyATP) and an inhibitor (Mavacamten), indicating structural similarity between R403Q and controls in these two states. ATPase assays reveal increased resting ATPase activity in R403Q samples, which persists even in the presence of 2-deoxyATP, suggesting that the elevated energy consumption in the R403Q mutation is driven by both a population shift toward the ON state and enhanced myosin ATPase activity per motor head.
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 0th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Estimation of crossbridge-state during cardiomyocyte beating using second harmonic generation
T. M. Watanabe, H. Fujita, … S. Miyagawa·bioRxiv·Oct 13, 2022
- Molecular mechanisms of altered contraction with the β-myosin R403Q mutation in porcine ventricular muscle and a human stem cell-derived cardiomyocyte model.
Sonette Steczina, Saffie E. Mohran, … Michael Regnier·Journal of Molecular and Cellular CardiologyPeer-reviewed·Oct 28, 2025
- The hypertrophic cardiomyopathy mutation G768R makes cardiac myosin a high duty ratio motor
Divya Pathak, T Ozturk Dalpe, … Kathleen M. Ruppel·bioRxiv·Jun 6, 2026
- Hypertrophic cardiomyopathy β-cardiac myosin mutation (P710R) leads to hypercontractility by disrupting super-relaxed state: multiscale measurements and computational modeling
A. S. Vander Roest, C. Liu, … D. Bernstein·bioRxiv·Nov 10, 2020
- The molecular basis of hypercontractility caused by the hypertrophic cardiomyopathy mutations R403Q and R663H
S. S. Sarkar, D. V. Trivedi, … J. A. Spudich·bioRxiv·Feb 7, 2019
- Cardiomyopathy Mutations Impact the Power Stroke of Human Cardiac Myosin
W. Tang, J. Ge, … C. M. Yengo·bioRxiv·Dec 8, 2020