Evidence of Surface Diffusion of Water Molecules on Proteins of Rabbit Lens by NMR Relaxation Measurements

1996 ◽  
Vol 51 (1-2) ◽  
pp. 81-90 ◽  
Author(s):  
Jerzy Bodurka ◽  
Gerd Buntkowsky ◽  
Aleksander Gutsze

Abstract In this work, we propose a relaxation model for the interpretation of NMR proton spinlattice and spin-spin relaxation times of mammalian lenses. The framework for this model is based on nuclear magnetic spin-lattice relaxation measurements as a function of tem perature at different Larmor frequencies for whole rabbit lenses and fragments of the lens. According to this model, two different dynamic processes of the water molecules determine the relaxation behaviour, namely rotational diffusion and translational surface diffusion. These dynamic processes in conjuction with a two site exchange model give a good explanation of all the measured relaxation data. From the experimental data, we were able to obtain the activation parameters for rotational and translational diffusion of bound lens water. Correlation times of 2.1×10-11 sec and 2.5×10-9 sec and activation energies of 20.5 kJ/mol and 22.5 kJ/mol respectively were found at 308K. At low Larmor frequencies (≤ MHz) the longitudinal relaxation is mainly determined by translational surface diffusion of bound water with a mean square displacement of 1.5 nm, whereas at higher frequencies (≥300 MHz), rotational diffusion is the main relaxation mechanism. The spin-spin relaxation is determined by translational diffusion over the whole frequency range and therefore shows only a very small dispersion. By our model it is possible to explain: 1) the strikingly large difference between the T1 value and the T2A and T2B values observed in the lens and 2 ) the different values of the activation energies measured at different fields for the lens.

2020 ◽  
Vol 73 (8) ◽  
pp. 734
Author(s):  
W. A. Monika Madhavi ◽  
Samantha Weerasinghe ◽  
Konstantin I. Momot

Rotational motion of molecules plays an important role in determining NMR spin relaxation properties of liquids. The textbook theory of NMR spin relaxation predominantly uses the assumption that the reorientational dynamics of molecules is described by a continuous time rotational diffusion random walk with a single rotational diffusion coefficient. Previously we and others have shown that reorientation of water molecules on the timescales of picoseconds is not consistent with the Debye rotational-diffusion model. In particular, multiple timescales of molecular reorientation were observed in liquid water. This was attributed to the hydrogen bonding network in water and the consequent presence of collective rearrangements of the molecular network. In order to better understand the origins of the complex reorientational behaviour of water molecules, we carried out molecular dynamics (MD) simulations of a liquid that has a similar molecular geometry to water but does not form hydrogen bonds: hydrogen sulfide. These simulations were carried out at T=208K and p=1 atm (~5K below the boiling point). Ensemble-averaged Legendre polynomial functions of hydrogen sulfide exhibited a Gaussian decay on the sub-picosecond timescale but, unlike water, did not exhibit oscillatory behaviour. We attribute these differences to hydrogen sulfide’s absence of hydrogen bonding.


1974 ◽  
Vol 47 (5) ◽  
pp. 1127-1135
Author(s):  
Geoffrey Allen ◽  
J. S. Higgins ◽  
C. J. Wright

Abstract Neutron scattering experiments on polymethylphenylsiloxane, poly(propylene oxide), poly(isobutylene), and poly(ethylene oxide) show broadening in the quasi-elastic region similar to that previously reported from polydimethylsiloxane. Measurements on partially deuterated samples confirm that the effect arises from segmental diffusive motion, rather than rotations of pendent side groups. The temperature dependence of this motion gives activation energies which are smaller than the activation energies for self-diffusion obtained from experiments of longer time-scale such as nuclear spin-lattice relaxation measurements and viscometry.


1965 ◽  
Vol 43 (6) ◽  
pp. 986-1000 ◽  
Author(s):  
Gerald A. De Wit ◽  
Myer Bloom

The deuteron spin–lattice relaxation time T1 and spin–spin relaxation time T2 have been studied in CD4 and CD3H between 55 °K and 110 °K. T1 was found to increase very slowly with temperature over the entire temperature range for CD4 with no measurable change being observable at the melting point. Since the deuteron spin relaxation is produced by intramolecular quadrupolar interactions, these results are in strong disagreement with the Debye rotational diffusion model often used to describe molecular reorientation. These results have been used to reanalyze the proton T1 data for CH4−nDn previously given by Bloom and Sandhu. The contributions to T1 from intermolecular dipolar interactions were found to be in close agreement with theory. Contributions from the spin–rotation interaction were found to be extremely small or zero in this temperature range. The effects of translational diffusion on the proton and deuteron T1 and T2 just below the melting point are also discussed.


1973 ◽  
Vol 51 (7) ◽  
pp. 1107-1108 ◽  
Author(s):  
B. A. Dunell ◽  
M. D. Pachal ◽  
S. E. Ulrich

The results of spin–lattice relaxation measurements are reported for carbonatotetramminecobalt(III) sulfate. The observed TI minima and activation energies, 1.9 and 4.3 kcal, for the reorientation of ammine groups are interpreted on the basis of hydrogen bonding effects.


1975 ◽  
Vol 30 (6-7) ◽  
pp. 883-890 ◽  
Author(s):  
F. Köksal ◽  
G. J. Krüger

Abstract The electron relaxation times T1 and T2 have been measured by ESR pulse techniques in solutions of normal and perdeuterated (diphenyl)- in dimethoxyethane at various radical concentrations and temperatures. The results are discussed in terms of different relaxation mechanisms. The most important contribution to spin-lattice relaxation at high concentration is dipolar interaction with other radical electrons modulated by translational diffusion. Spin-spin relaxation has in addition contributions from electron exchange and ion pairing.


2003 ◽  
Vol 772 ◽  
Author(s):  
M. Schmid ◽  
C. Goze-Bac ◽  
M. Mehring ◽  
S. Roth ◽  
P. Bernier

AbstractLithium intercalted carbon nanotubes have attracted considerable interest as perspective components for energy storage devices. We performed 13C Nuclear Magnetic Resonance spin lattice relaxation measurements in a temperature range from 4 K up to 300 on alkali intercalated Single Walled Carbon Nanotubes in order to investigate the modifications of the electronic properties. The density of states at the Fermi level were determined for pristine, lithium and cesium intercalated carbon nanotubes and are discussed in terms of intercalation and charge transfer effects.


1997 ◽  
Vol 30 (22) ◽  
pp. 6869-6872 ◽  
Author(s):  
R. Jaeger ◽  
G. J. Vancso ◽  
D. Gates ◽  
Y. Ni ◽  
I. Manners

Sign in / Sign up

Export Citation Format

Share Document