Origin of Protein Quake: Energy Waves Conducted by a Precise Mechanical Machine
Abstract
A long-standing challenge in protein biophysics is to understand protein quake in myoglobin--the structural dynamics responsible for redistributing the excess heme energy after photolysis. Despite extensive efforts, the molecular mechanism of this process remains elusive. Using the energy flow theory, we uncovered a fundamental new phenomenon: the heme energy is redistributed by energy waves with a ubiquitous fundamental frequency and two overtones. Energy waves emanate from the heme into the myoglobin backbone via a conduit of five consecutive dihedrals of the proximal histidine, then travel quickly along the backbone to reach sidechains across the protein. This mechanism is far more effective than the diffusion-based mechanism from previous studies because waves are systematic while diffusion is random. To propagate energy waves, coordinates must cooperate, resulting in collective modes that are singular vectors of the generalized work functional. These modes show task partitioning: a handful of high-energy modes generate large-scale breathing motion, which loosens up the protein matrix to enable hundreds of low-energy vibrational modes for energy transduction.
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
- Molecular dynamics simulations and linear response theories jointly describe biphasic responses of myoglobin relaxation and reveal evolutionarily conserved frequent communicators
B.-C. Huang, L.-W. Yang·bioRxiv·Jul 2, 2019
- Collective Excitations in α-helical Protein Structures Interacting with the Water Environment
V. N. Kadantsev, A. Goltsov·bioRxiv·Apr 15, 2020
- Long-Range Hopping Conductivity in Proteins
S. Krishnan, A. Aksimentiev, … D. Matyushov·bioRxiv·Oct 27, 2022
- Decoupling of the Onset of Anharmonicity between a Protein and Its Surface Water around 200 K
- Molecular fluctuations as a ruler of force-induced protein conformations
A. Stannard, M. Mora, … S. Garcia-Manyes·bioRxiv·Dec 18, 2020
- Slow conformational exchange and overall rocking motion in ubiquitin protein crystals
V. Kurauskas, S. A. Izmailov, … P. Schanda·bioRxiv·Jun 2, 2017