ArticleThe Journal of chemical physics2018
Communication: Transition-path velocity as an experimental measure of barrier crossing dynamics.
Article in The Journal of chemical physics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- The significance of fuzzy boundaries of the barrier regions in single-molecule measurements of failed barrier crossing attempts.The Journal of chemical physics · 2024Article
- Article
- The Effect of Time Resolution on Apparent Transition Path Times Observed in Single-Molecule Studies of Biomolecules.The journal of physical chemistry. B · 2022Article
- On distributions of barrier crossing times as observed in single-molecule studies of biomolecules.Biophysical reports · 2021Article
- Estimating transition path times and shapes from single-molecule photon trajectories: A simulation analysis.The Journal of chemical physics · 2021Article
- ART-RRT: As-Rigid-As-Possible search for protein conformational transition paths.Journal of computer-aided molecular design · 2019Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Experimental observation of transition paths-short events when the system of interest crosses the free energy barrier separating reactants from products-provides an opportunity to probe the dynamics of barrier crossing. Yet limitations in the experimental time resolution usually result in observing trajectories that are smoothed out, recross the transition state fewer times, and exhibit apparent velocities that are much lower than the instantaneous ones. Here we show that it is possible to define (and measure) an effective transition-path velocity which preserves exact information about barrier crossing dynamics in the following sense: the exact transition rate can be written in a form resembling that given by transition-state theory, with the mean thermal velocity replaced by the transition-path velocity. In addition, the transition-path velocity (i) ensures the exact local value of the unidirectional reactive flux at equilibrium and (ii) leads to the exact mean transition-path time required for the system to cross the barrier region separating reactants from products. We discuss the coordinate dependence of the transition path velocity and derive analytical expressions for it in the case of diffusive dynamics. These results can be used to discriminate among models of barrier crossing dynamics in single-molecule force spectroscopy studies.
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Registered trials
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