1. Volume 83, Issue 4, Pages 1854-1866 (October 2002)
Molecular Dynamics Simulation of Site-Directed Spin Labeling: Experimental Validation in Muscle Fibers 
Leslie E.W. LaConte, Vincent Voelz, Wendy Nelson, Michael Enz, David D. Thomas 
Biophysical Journal 
Volume 83, Issue 4, Pages (October 2002)
DOI: /S (02)
Copyright © 2002 The Biophysical Society Terms and Conditions

2. Figure 1
(A) Models of several experimental mutants produced by site-directed mutagenesis were constructed in InsightII: C108 (wild type), A105C, M129C, and D131C. Other “predicted” mutants were also constructed: M60C, M72C, and G95C. (B) Spin label FDNASL and its partial charges.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

3. Figure 2
Geometry of the spin probe. H is the laboratory-frame magnetic field, oriented with spherical angles θ, ϕ with the nitroxide z axis.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

4. Figure 3
Relationship between orientational trajectory β(t) and order parameter S. β is the angle between the z axis of the spin label and the mode vector, which defines the center of the orientational distribution ρ(β). S is calculated from ρ.(β) as described in Eq. 1.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

5. Figure 4
Spectral line-splittings are used to calculate order parameter (S) from an EPR spectrum according to Eq. 2 (spectrum example shown is of spin-labeled M129C in randomly oriented fibers).
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

6. Figure 5
Typical convergence of MD trajectories, shown here for the myosin regulatory domain spin-labeled at C108. (A) Total potential energy. (B) The RMS difference in atom positions, including all movable atoms, relative to the starting conformation. (C) First 150ps of an MD trajectory in which velocity perturbations were applied every 50ps (as marked by arrows).
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

7. Figure 6
Order parameters of C108-FDNASL trajectories shown as a function of the radius of allowed motion. Points plotted are mean±SE of order parameter across 1-ns trajectory segments.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

8. Figure 7
Convergence sensitivity to starting conformer. The average potential energy of each local minimal conformer is plotted, and its respective order parameter is shown below each data point.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

9. Figure 8
EPR spectra and simulated spin probe trajectories over 14ns for randomly oriented FDNASL-labeled regulatory domains for seven different sites. (Left) Experimental EPR spectrum and order parameter S. (Middle) Orientational trajectory of the spin label in which the angle β (Fig. 3) is plotted over time. (Right) Probability distribution ρ(β) over the entire trajectory.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

10. Figure 9
(A) Average D131C-FDNASL and Arg-813 conformers over the first 9ns of the MD trajectory (red) and over last 5ns of the trajectory (green). The heavy chain helix is shown as a blue ribbon. A different rotamer for Arg-813 produces a shift in the steric boundaries of the probe on a time scale of several nanoseconds. (B) Simulated annealing of A105C-FDNASL found three conformers—pick1, pick2, and pick3—representing local minima similar to within average probe RMS differences<1.6Å (pick1-pick2=1.55, pick2-pick3=1.64, pick1-pick3=0.60)
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

11. Figure 10
Autocorrelations of trajectory D131C at 300 and 600K. Probe trajectory autocorrelations for D131C are only approximately exponential. Here first-order decays are fit over 500ps of the trajectory as a function of temperature.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions

12. Figure 11
Experimental (black) order parameters of spin-labeled mutants determined by EPR spectroscopy, plotted against simulated (white) order parameters calculated directly from molecular dynamics trajectories. Error bars in the simulated values are the standard deviation of order parameters across 1-ns segments. For A105C, three trajectories were simulated, but only the order parameter for the dynamics trajectory about the lowest-energy minimum is shown.
Biophysical Journal  , DOI: ( /S (02) )
Copyright © 2002 The Biophysical Society Terms and Conditions