A structure-based simulation approach for electron paramagnetic resonance spectra using molecular and stochastic dynamics simulations

Autor(en): Beier, Christian
Steinhoff, Heinz-Jurgen 
Stichwörter: ANGSTROM RESOLUTION; BACTERIORHODOPSIN; Biophysics; BROWNIAN DYNAMICS; CRYSTAL-STRUCTURE; EPR-SPECTROSCOPY; NITROXIDE SIDE-CHAINS; PROTEIN DYNAMICS; PROTON TRANSLOCATION; SPIN LABEL; T4 LYSOZYME
Erscheinungsdatum: 2006
Herausgeber: CELL PRESS
Journal: BIOPHYSICAL JOURNAL
Volumen: 91
Ausgabe: 7
Startseite: 2647
Seitenende: 2664
Zusammenfassung: 
Electron paramagnetic resonance (EPR) spectroscopy using site-directed spin-labeling is an appropriate technique to analyze the structure and dynamics of flexible protein regions as well as protein-protein interactions under native conditions. The analysis of a set of protein mutants with consecutive spin-label positions leads to the identification of secondary and tertiary structure elements. In the first place, continuous-wave EPR spectra reflect the motional freedom of the spin-label specifically linked to a desired site within the protein. EPR spectra calculations based on molecular dynamics ( MD) and stochastic dynamics simulations facilitate verification or refinement of predicted computer-aided models of local protein conformations. The presented spectra simulation algorithm implies a specialized in vacuo MD simulation at 600 K with additional restrictions to sample the entire accessible space of the bound spin-label without large temporal effort. It is shown that the distribution of spin-label orientations obtained from such MD simulations at 600 K agrees well with the extrapolated motion behavior during a long timescale MD at 300 K with explicit water. The following potential-dependent stochastic dynamics simulation combines the MD data about the site-specific orientation probabilities of the spin-label with a realistic rotational diffusion coefficient yielding a set of trajectories, each more than 700 ns long, essential to calculate the EPR spectrum. Analyses of a structural model of the loop between helices E and F of bacteriorhodopsin are illustrated to demonstrate the applicability and potentials of the reported simulation approach. Furthermore, effects on the motional freedom of bound spin-labels induced by solubilization of bacteriorhodopsin with Triton X-100 are examined.
ISSN: 00063495
DOI: 10.1529/biophysj.105.080051

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