Master equations are widely used for modeling protein folding. Here an approximate solution to such master equations is presented. The approach used may be viewed as a discrete variational transition-state theory. The folding rate constant kf is approximated by the outgoing reaction flux J, when the unfolded set of macrostates assumes an equilibrium distribution. Correspondingly the unfolding rate constant ku is calculated as Jpu(1-pu), where pu is the equilibrium fraction of the unfolded state. The dividing surface between the unfolded and folded states is chosen to minimize the reaction flux J. This minimum-reaction-flux surface plays the role of the transition-state ensemble and identifies rate-limiting steps. Test against exact results of master-equation models of Zwanzig [Proc. Natl. Acad. Sci. USA 92, 9801 (1995)] and Munoz et al. [Proc. Natl. Acad. Sci. USA 95, 5872 (1998)] shows that the minimum-reaction-flux solution works well. Macrostates separated by the minimum-reaction-flux surface show a gap in p(fold) values. The approach presented here significantly simplifies the solution of master-equation models and, at the same time, directly yields insight into folding mechanisms.
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http://dx.doi.org/10.1063/1.2929824 | DOI Listing |
J Phys Chem A
January 2025
Department of Mechanical Engineering, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR 999077, China.
An adequate understanding of the NO interacting chemistry is a prerequisite for a smoother transition to carbon-lean and carbon-free fuels such as ammonia and hydrogen. In this regard, this study presents a comprehensive study on the H atom abstraction by NO from C to C alkynes, dienes, and trienes forming 3 HNO isomers (i.e.
View Article and Find Full Text PDFJ Phys Chem A
December 2024
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
Radical-radical reaction channels are important in the pyrolysis and oxidation chemistry of perfluoroalkyl substances (PFAS). In particular, unimolecular dissociation reactions within unbranched -perfluoroalkyl chains, and their corresponding reverse barrierless association reactions, are expected to be significant contributors to the gas-phase thermal decomposition of families of species such as perfluorinated carboxylic acids and perfluorinated sulfonic acids. Unfortunately, experimental data for these reactions are scarce and uncertain.
View Article and Find Full Text PDFACS Earth Space Chem
December 2024
School of Chemistry, University of Leeds, Leeds LS2 9JT, U.K.
Rate coefficients for the reaction of CH with CHO were measured for the first time over the temperature range of 37-603 K, with the CH radicals produced by pulsed laser photolysis and detected by CH radical chemiluminescence following their reaction with O. The low temperature measurements (≤93 K) relevant to the interstellar medium were made within a Laval nozzle gas expansion, while higher temperature measurements (≥308 K) were made within a temperature controlled reaction cell. The rate coefficients display a negative temperature dependence below 300 K, reaching (1.
View Article and Find Full Text PDFComput Struct Biotechnol J
December 2024
Department of Physics and Astronomy, University of Calgary, Calgary, AB, T2N 1N4, Canada.
Recent studies and suggest that flavin adenine dinucleotide (FAD) on its own might be able to act as a biological magnetic field sensor. Motivated by these observations, in this study, we develop a detailed quantum theoretical model for the radical pair mechanism (RPM) for the flavin adenine biradical within the FAD molecule. We use the results of existing molecular dynamics simulations to determine the time-varying distance between the radicals on FAD, which we then feed into a quantum master equation treatment of the RPM.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Center for Combustion Energy, Tsinghua University, Beijing 100084, People's Republic of China.
The change of the vibrational energy within a molecule after collisions with another molecule plays an essential role in the evolution of molecular internal energy distributions, which is also the limiting process in the relaxation of gases toward equilibrium. Here, we investigate the energy transfer between the translational motion and the vibrational motion of the diatom during the atom-diatom collision, the simplest case involving the transfer between inter-molecular and intra-molecular energies. We are interested in the situation when the translational temperature of the gas is high, in which case, there are significant probabilities for the vibrational energy to change over widely separated energy levels after a collision.
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