In this reporting period, four papers appeared in print dealing with (1) the decomposition of free energies (2) the theory and simulation of the rate of diffusion influenced chemical reaction (3) the relationship between first passage times, correlation functions and reaction rates and (4) the influence of high intensity laser pulses on fluorescence quenching. These will now be briefly described in turn. The problem of decomposing the total free energy of binding of a ligand to a protein into electrostatic Van der Waals etc. components has recently been a subject of great interest and controversy. We have been able to show that by expressing the free energy perturbation expansion in terms of temperature derivatives of the mean energy, a natural and useful decomposition of the free energy into components corresponding to each term in the Hamiltonian can be obtained. Many biological processes such as ligand binding to receptors, enzyme-substrate complex formation, protein DNA association, can often be described as diffusion influenced reactions. The rate of such reactions can only be obtained analytically for idealized (and unrealistic) models. We have developed a comprehensive theoretical framework to treat these reactions which leads to novel and efficient ways of obtaining the rates using Brownian dynamics computer simulations. A fundamental problem in chemical kinetics is how to calculate the rate of unimolecular reactions (such as isomerization) from the microscopic dynamics. Over the years several alternate definitions were proposed based on the theory of first passage times for irreversible processes and on the equilibrium fluctuations of certain quantities as determined by correlation functions. We have been able to find a rigorous relationship between these seemingly different approaches that clarify the circumstances under which they are equivalent. Finally, we have been able to solve the controversial and long outstanding problem of how one should theoretically treat excitation pulses in fluorescence quenching experiments. Our work indicates how such experiments should be correctly interpreted.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Intramural Research (Z01)
Project #
1Z01DK029019-18
Application #
6105203
Study Section
Special Emphasis Panel (LCP)
Project Start
Project End
Budget Start
Budget End
Support Year
18
Fiscal Year
1998
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Berezhkovskii, Alexander; Hummer, Gerhard; Szabo, Attila (2009) Reactive flux and folding pathways in network models of coarse-grained protein dynamics. J Chem Phys 130:205102
Gopich, Irina V; Nettels, Daniel; Schuler, Benjamin et al. (2009) Protein dynamics from single-molecule fluorescence intensity correlation functions. J Chem Phys 131:095102
Bezrukov, Sergey M; Berezhkovskii, Alexander M; Szabo, Attila (2007) Diffusion model of solute dynamics in a membrane channel: mapping onto the two-site model and optimizing the flux. J Chem Phys 127:115101
Dudko, Olga K; Mathe, Jerome; Szabo, Attila et al. (2007) Extracting kinetics from single-molecule force spectroscopy: nanopore unzipping of DNA hairpins. Biophys J 92:4188-95
Berezhkovskii, Alexander; Szabo, Attila (2006) Perturbation theory of Phi-value analysis of two-state protein folding: relation between p fold and Phi values. J Chem Phys 125:104902
Dudko, Olga K; Hummer, Gerhard; Szabo, Attila (2006) Intrinsic rates and activation free energies from single-molecule pulling experiments. Phys Rev Lett 96:108101
Gopich, Irina; Szabo, Attila (2005) Fluorophore-quencher distance correlation functions from single-molecule photon arrival trajectories. J Phys Chem B 109:6845-8
Berezhkovskii, Alexander; Szabo, Attila (2005) One-dimensional reaction coordinates for diffusive activated rate processes in many dimensions. J Chem Phys 122:14503
Gopich, Irina V; Szabo, Attila (2005) Photon counting histograms for diffusing fluorophores. J Phys Chem B 109:17683-8
Gopich, Irina; Szabo, Attila (2005) Theory of photon statistics in single-molecule Forster resonance energy transfer. J Chem Phys 122:14707

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