Switch-1 Instability at the Active Site Decouples ATP Hydrolysis from Force Generation in Myosin II
Abstract
Myosin active site elements (i.e. switch-1) bind both ATP and a divalent metal to coordinate ATP hydrolysis. ATP hydrolysis at the active site is linked via allosteric communication to the actin polymer binding site and lever arm movement, thus coupling the free energy of ATP hydrolysis to force generation. How active site motifs are functionally linked to actin binding and the power stroke is still poorly understood. We hypothesize that destabilizing switch-1 movement at the active site will negatively affect the tight coupling of ATP hydrolysis to force production. Using a metal-switch system, we tested the effect of interfering with switch-1 coordination of the divalent metal cofactor on force generation. We found that while ATPase activity increased, motility was inhibited. Our results demonstrate that a single atom change that affects the switch-1 interaction with the divalent metal directly regulates actin binding and force generation. Even slight modification of the switch-1 divalent metal coordination can decouple ATP hydrolysis from motility. Switch-1 movement is therefore critical for both structural communication with the actin binding site, as well as coupling the energy of ATP hydrolysis to force generation.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility 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
- Electrostatic interaction of loop 1 and backbone of human cardiac myosin regulates the rate of ATP induced actomyosin dissociation
A. G. Iragavarapu, Y. Nesmelov·bioRxiv·Oct 8, 2021
- High resolution structures of Myosin-IC reveal a unique actin-binding orientation, ADP release pathway, and power stroke trajectory
Sai Shashank Chavali, Peter J. Carman, … Charles Vaughn Sindelar·Proceedings of the National Academy of SciencesPeer-reviewed·Feb 27, 2025
- The central role of the tail in switching off myosin II in cells
- Coupling of ATPase activity, microtubule binding and mechanics in the dynein motor domain
S. Niekamp, N. Coudray, … G. Bhabha·bioRxiv·Jan 11, 2019
- Structural transitions in kinesin minus-end directed microtubule motility
Satoki Shibata, Matthew Y. Wang, … Ryo Nitta·Scientific ReportsPeer-reviewed·Jan 5, 2026
- Mechanistic Insights Into The Active Site And Allosteric Communication Pathways In Human Nonmuscle Myosin-2C
K. Chinthalapudi, S. M. Heissler, … D. J. Manstein·bioRxiv·May 17, 2017