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Dynamic autocorrelation function

Figure 2.15 Illustration of the use of autocorrelation to probe conformational dynamics. Autocorrelation functions are measured for the kinetic sample (top, solid line) and the control sample (top, broken line), which has no dynamic conformational component. The ratio of these autocorrelation functions leaves only the conformational dynamics component (bottom, grey broken line) which can be fit with, in this case, a stretched exponential (bottom, solid black line) to extract the observed rate constant for the transition. In this case the dynamic sample was an RNA hairpin labelled with fluorescein. When the hairpin was formed the dye was brought near a quencher, thus modulating the fluorescence emission and providing fluctuations to be probed via autocorrelation. The control sample lacked the quencher. Figure 2.15 Illustration of the use of autocorrelation to probe conformational dynamics. Autocorrelation functions are measured for the kinetic sample (top, solid line) and the control sample (top, broken line), which has no dynamic conformational component. The ratio of these autocorrelation functions leaves only the conformational dynamics component (bottom, grey broken line) which can be fit with, in this case, a stretched exponential (bottom, solid black line) to extract the observed rate constant for the transition. In this case the dynamic sample was an RNA hairpin labelled with fluorescein. When the hairpin was formed the dye was brought near a quencher, thus modulating the fluorescence emission and providing fluctuations to be probed via autocorrelation. The control sample lacked the quencher.
In an ambitious study, the AIMS method was used to calculate the absorption and resonance Raman spectra of ethylene [221]. In this, sets starting with 10 functions were calculated. To cope with the huge resources required for these calculations the code was parallelized. The spectra, obtained from the autocorrelation function, compare well with the experimental ones. It was also found that the non-adiabatic processes described above do not influence the spectra, as their profiles are formed in the time before the packet reaches the intersection, that is, the observed dynamic is dominated by the torsional motion. Calculations using the Condon approximation were also compared to calculations implicitly including the transition dipole, and little difference was seen. [Pg.309]

A powerful analytical tool is the time correlation function. For any dynamic variable A (it), such as bond lengths or dihedral angles, the time autocorrelation function Cy) is defined... [Pg.54]

Fig. 13 shows this autocorrelation function where the time is scaled by mean square displacement of the center of mass of the chains normalized to Ree)- All these curves follow one common function. It also shows that for these melts (note that the chains are very short ) the interpretation of a chain dynamics within the Rouse model is perfectly suitable, since the time is just given within the Rouse scaling and then normalized by the typical extension of the chains [47]. [Pg.504]

Short-time Brownian motion was simulated and compared with experiments [108]. The structural evolution and dynamics [109] and the translational and bond-orientational order [110] were simulated with Brownian dynamics (BD) for dense binary colloidal mixtures. The short-time dynamics was investigated through the velocity autocorrelation function [111] and an algebraic decay of velocity fluctuation in a confined liquid was found [112]. Dissipative particle dynamics [113] is an attempt to bridge the gap between atomistic and mesoscopic simulation. Colloidal adsorption was simulated with BD [114]. The hydrodynamic forces, usually friction forces, are found to be able to enhance the self-diffusion of colloidal particles [115]. A novel MC approach to the dynamics of fluids was proposed in Ref. 116. Spinodal decomposition [117] in binary fluids was simulated. BD simulations for hard spherocylinders in the isotropic [118] and in the nematic phase [119] were done. A two-site Yukawa system [120] was studied with... [Pg.765]

An examination of the autocorrelation function (0(0) <2(0) annucleophilic attack step in the catalytic reaction of subtilisin is presented in Fig. 9.4. As seen from the figure, the relaxation times for the enzymatic reaction and the corresponding reference reaction in solution are not different in a fundamental way and the preexponential factor t 1 is between 1012 and 1013 sec-1 in both cases. As long as this is the case, it is hard to see how enzymes can use dynamical effects as a major catalytic factor. [Pg.216]

FIGURE 9.4. The autocorrelation function of the time-dependent energy gap Q(t) = (e3(t) — 2(0) for the nucleophilic attack step in the catalytic reaction of subtilisin (heavy line) and for the corresponding reference reaction in solution (dotted line). These autocorrelation functions contain the dynamic effects on the rate constant. The similarity of the curves indicates that dynamic effects are not responsible for the large observed change in rate constant. The autocorrelation times, tq, obtained from this figure are 0.05 ps and 0.07ps, respectively, for the reaction in subtilisin and in water. [Pg.216]

For the analysis of the dynamical properties of the water and ions, the simulation cell is divided into eight subshells of thickness 3.0A and of height equal to the height of one turn of DNA. The dynamical properties, such as diffusion coefficients and velocity autocorrelation functions, of the water molecules and the ions are computed in various shells. From the study of the dipole orientational correlation function... [Pg.253]

Fluorescence intensity detected with a confocal microscope for the small area of diluted solution temporally fluctuates in sync with (i) motions of solute molecules going in/out of the confocal volume, (ii) intersystem crossing in the solute, and (hi) quenching by molecular interactions. The degree of fluctuation is also dependent on the number of dye molecules in the confocal area (concentration) with an increase in the concentration of the dye, the degree of fluctuation decreases. The autocorrelation function (ACF) of the time profile of the fluorescence fluctuation provides quantitative information on the dynamics of molecules. This method of measurement is well known as fluorescence correlation spectroscopy (FCS) [8, 9]. [Pg.139]

As mentioned in the introductory part of this section, quantum dots exhibit quite complex non-radiative relaxation dynamics. The non-radiative decay is not reproduced by a single exponential function, in contrast to triplet states of fluorescent organic molecules that exhibit monophasic exponential decay. In order to quantitatively analyze fluorescence correlation signals of quantum dots including such complex non-radiative decay, we adopted a fluorescence autocorrelation function including the decay component of a stretched exponential as represented by Eq. (8.11). [Pg.148]

In addition to the fact that MPC dynamics is both simple and efficient to simulate, one of its main advantages is that the transport properties that characterize the behavior of the macroscopic laws may be computed. Furthermore, the macroscopic evolution equations can be derived from the full phase space Markov chain formulation. Such derivations have been carried out to obtain the full set of hydrodynamic equations for a one-component fluid [15, 18] and the reaction-diffusion equation for a reacting mixture [17]. In order to simplify the presentation and yet illustrate the methods that are used to carry out such derivations, we restrict our considerations to the simpler case of the derivation of the diffusion equation for a test particle in the fluid. The methods used to derive this equation and obtain the autocorrelation function expression for the diffusion coefficient are easily generalized to the full set of hydrodynamic equations. [Pg.99]

In the canonical ensemble (P2) = 3kBTM and p M. In the microcanonical ensemble (P2) = 3kgT i = 3kBTMNm/(M + Nm) [49]. If the limit M —> oo is first taken in the calculation of the force autocorrelation function, then p = Nm and the projected and unprojected force correlations are the same in the thermodynamic limit. Since MD simulations are carried out at finite N, the study of the N (and M) dependence of (u(t) and the estimate of the friction coefficient from either the decay of the momentum or force correlation functions is of interest. Molecular dynamics simulations of the momentum and force autocorrelation functions as a function of N have been carried out [49, 50]. [Pg.116]

The Langevin dynamics method simulates the effect of individual solvent molecules through the noise W, which is assumed to be Gaussian. The friction coefficient r is related to the autocorrelation function of W through the fluctuation-dissipation theorem,... [Pg.242]

The linear response theory [50,51] provides us with an adequate framework in order to study the dynamics of the hydrogen bond because it allows us to account for relaxational mechanisms. If one assumes that the time-dependent electrical field is weak, such that its interaction with the stretching vibration X-H Y may be treated perturbatively to first order, linearly with respect to the electrical field, then the IR spectral density may be obtained by the Fourier transform of the autocorrelation function G(t) of the dipole moment operator of the X-H bond ... [Pg.247]

NMR 13C spin-lattice relaxation times are sensitive to the reorientational dynamics of 13C-1H vectors. The motion of the attached proton(s) causes fluctuations in the magnetic field at the 13C nuclei, which results in decay of their magnetization. Although the time scale for the experimentally measured decay of the magnetization of a 13C nucleus in a polymer melt is typically on the order of seconds, the corresponding decay of the 13C-1H vector autocorrelation function is on the order of nanoseconds, and, hence, is amenable to simulation. [Pg.42]

To conclude, the results presented in this section demonstrate that the semiclassical implementation of the mapping approach is able to describe rather well the ultrafast dynamics of the nonadiabatic systems considered. In particular, it is capable of describing the correct relaxation dynamics of the autocorrelation function as well as the structures of the absorption spectrum of... [Pg.354]

The results obtained for the three-mode Model IVb are depicted in Fig. 45. As was found for the semiclassical mapping approach, the spin-coherent state propagators can only reproduce the short-time dynamics for the electronic population. The autocorrelation function, on the other hand, is reproduced at least qualitatively correctly by the semiclassical spin-coherent state propagator. [Pg.361]

This effective Q,t-range overlaps with that of DLS. DLS measures the dynamics of density or concentration fluctuations by autocorrelation of the scattered laser light intensity in time. The intensity fluctuations result from a change of the random interference pattern (speckle) from a small observation volume. The size of the observation volume and the width of the detector opening determine the contrast factor C of the fluctuations (coherence factor). The normalized intensity autocorrelation function g Q,t) relates to the field amplitude correlation function g (Q,t) in a simple way g t)=l+C g t) if Gaussian statistics holds [30]. g Q,t) represents the correlation function of the fluctuat-... [Pg.22]

The theory of statistical mechanics provides the formalism to obtain observables as ensemble averages from the microscopic configurations generated by such a simulation. From both the MC and MD trajectories, ensemble averages can be formed as simple averages of the properties over the set of configurations. From the time-ordered properties of the MD trajectory, additional dynamic information can be calculated via the time correlation function formalism. An autocorrelation function Caa( = (a(r) a(t + r)) is the ensemble average of the product of some function a at time r and at a later time t + r. [Pg.404]

As the salt concentration continues to decrease, however, matters change dramatically Q). The total scattering intensity decreases more abruptly, and the QLS autocorrelation function, which has been a simple single-exponential decay, becomes markedly two-exponential. The two decay rates differ by as much as two orders of magnitude. The faster continues the upward trend of D pp from higher salt, and is thus assigned the term "ordinary . The slower, which is about 1/10 of Dapp high salt, and appears to reflect a new mode of solution dynamics, is termed "extraordinary . [Pg.206]

The autocorrelation function quantifies, on a unit scale, the degree to which a quantity is correlated with values of the same quantity at later times. The function can be meaningfully calculated for any dynamical simulation, in the sense defined earlier, and therefore including MC. We must consider a set of time-ordered values of the observable of interest, so that / — f(t — /At), with j — 1,2,..., N and At the time step between frames. (For MC simulations, one can... [Pg.47]

Dynamics of Reorientation. The approach of Impey, Madden and McDonald is used to consider the dynamics of reorientation for water molecules. The time autocorrelation function of the second Legrendre polynomial P2 of the angle subtended by the intramolecular H-H bond vector at time t with respect to its position at time t = 0 is calculated ... [Pg.96]

The Tr operation denotes a classical integration over all coordinates. Apart from the mean potential, the particle also feels a random force , = which is due to all the bath degrees of freedom. This random force has zero mean, and one can compute its autocorrelation function. The mapping of the tme dynamics onto the GLE is then completed by assuming that the random force (t) is Gaussian and its autocorrelation function is ( ,(t) ,(t )) = Y(t t ) where p =... [Pg.3]


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See also in sourсe #XX -- [ Pg.171 , Pg.172 ]




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