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1.
The relaxation in protein solutions has mainly been studied by nuclear magnetic relaxation dispersion (NMRD) techniques. NMRD data have mostly been analyzed in terms of fast chemical exchange of water between free water and water bound to proteins. Several approaches were used for the estimation of correlation time modulating the relaxation mechanism of bound water. On the other hand, in a nuclear magnetic resonance experiment, the relaxation rates of protein solutions (1/T1 and 1/T2) and also those of free water (1/T1f and 1/T2f) are measurable. However, the relaxation rates of bound water (1/T1b and 1/T2b) are not. Despite this, equating (1/T1-1/T1f)/2(1/T2-1/T2f) to (1/T1b)/2(1/T2b) leads to an expression involving only an effective tau that is related to the rotational correlation time (tau r) of proteins. Equating the ratios may therefore give a simple alternative method for the determination of tau r even if this method is limited to a single resonance frequency. In this work, a formula was derived for the solution of the effective tau. Then, the 1/T1 and 1/T2 in solutions of two globular proteins (lysozyme and albumin) and one nonglobular protein (gamma-globulin) were measured for different amounts of each protein. Next, the values of 1/T1 and 1/T2 were plotted vs. protein concentrations, and then the slopes of the fits were used in the derived equation for determining the effective tau values. Finally, the rotational correlation time tau r, calculated from tau, was used in the Stokes-Einstein relation to reproduce relevant radii. The effective tau values of lysozyme, albumin and gamma-globulin were found to be 5.89 ns, 7.03 ns and 8.8 ns, respectively. tau r values of albumin and lysozyme produce their Stokes radii. The present data suggest that use of the measurable ratio in the derived formula may give a simple way for the determination of the correlation times of lysozyme and albumin.  相似文献   

2.
A new theoretical model for nuclear spin relaxation in paramagnetic systems in solution has been developed. Fast rotational motion is included in the model, both as a source of modulation of the static zero-field splitting, which provides a mechanism for electron spin relaxation, and as an origin of the stochastic variation of the electron spin-nuclear spin dipole-dipole interaction leading to nuclear spin relaxation. At the limit of low magnetic field, the model is essentially identical to the earlier formulations from our laboratory, but new closed-form expressions are given for the inner- and outer-sphere relaxation at the high-field limit. Numerical comparisons with a general theory are reported for the inner-sphere case. In addition, some nuclear magnetic relaxation dispersion (NMRD) profiles from the literature are considered for systems where experiments have been done with both low-molecular weight paramagnetic complexes and their adducts with proteins. Previously developed theories are used to interpret data for the slowly rotating protein adducts, and good fits of the fast-rotating counterparts are obtained by further adjustment of one or two additional parameters.  相似文献   

3.
By combining magnetic field cycling in the range from 0.1mT to 7T with high-resolution NMR detection the T(1) relaxation dispersion (nuclear magnetic relaxation dispersion (NMRD)) of protons in the nucleotides adenosine mono-phosphate and guanosine mono-phosphate was measured in a site-specific way. While at high field the individual spins have distinctly different T(1) times, their scalar spin-spin interaction fulfills at low field the condition of strong coupling and leads to convergence of their T(1) dispersion curves. In addition, the spin-spin coupling can lead to oscillatory components in the relaxation kinetics traceable to a coupling between spin polarization and coherence in the relaxation process. As a consequence the NMRD curves do not directly reflect the spectral density function of the motional processes, but the effects of motion and spin coupling must be separated for a reliable evaluation. A theoretical approach is described allowing such an analysis.  相似文献   

4.
A theoretical study was made of magnetic field-dependent dipolar relaxation in two- and three-spin systems. The results for the nuclear magnetic relaxation dispersion (NMRD) curves were compared with those for the simpler model of fluctuating local fields. For both models it was found that at low fields spins tend to relax with a common T 1-relaxation time. Sharp features in the NMRD curves coming from nuclear spin level anti-crossings are also predicted by both models. However, the simple model fails to describe the behavior of so-called long-lived spin states (LLS). We have studied the LLS as function of magnetic field and molecular geometry and simulated experimental results for the LLS in histidine amino acid obtained at the laboratory of Prof. H.-M. Vieth (Free University Berlin, Germany). In addition, we described polarization transfer in a three-spin system where two spins are protons, which are initially hyperpolarized by para-hydrogen induced polarization (PHIP), while the third spin is a spin ½ hetero-nucleus, which acquires polarization in the course of cross-relaxation.  相似文献   

5.
Electron spin relaxation times of a Nycomed triarylmethyl radical (sym-trityl) in water, 1:1 water:glycerol, and 1:9 water:glycerol were measured at L-band, S-band, and X-band by pulsed EPR methods. In H(2)O solution, T(1) is 17+/-1 micros at X-band at ambient temperature, is nearly independent of microwave frequency, and exhibits little dependence on viscosity. The temperature dependence of T(1) in 1:1 water:glycerol is characteristic of domination by a Raman process between 20 and 80 K. The increased spin-lattice relaxation rates at higher temperatures, including room temperature, are attributed to a local vibrational mode that modulates spin-orbit coupling. In H(2)O solution, T(2) is 11+/-1 micros at X-band, increasing to 13+/-1 micros at L-band. For more viscous solvent mixtures, T(2) is much shorter than T(1) and weakly frequency dependent, which indicates that incomplete motional averaging of hyperfine anisotropy makes a significant contribution to T(2). In water and 1:1 water:glycerol solutions continuous wave EPR linewidths are not relaxation determined, but become relaxation determined in the higher viscosity 1:9 water:glycerol solutions. The Lorentzian component of the 250-MHz linewidths as a function of viscosity is in good agreement with T(2)-determined contributions to the linewidths at higher frequencies.  相似文献   

6.
The magnetic susceptibility of two complex ferric compounds in both the solid state and solution — ferric ammonium citrate and potassium (hexa)cyanoferrate (III) — was measured. On the basis of measurements of other physical constants the magnetic moments were calculated from the susceptibility and with citrate also from the longitudinal relaxation time of nuclear magnetic resonance. Some magnetic measurements of these substances made hitherto were verified and missing data were found. The results show that for citrate the magnetic moment from both the solid state and solution is smaller than purely spin moment, which confirms the opinion that it is a mixture of several components having different values of the Weiss constant. With potassium ferricyanide the opposite is the case, which indicates that the orbital moment, the contribution of which in the solid state is relatively larger than in solutions, is not quite suppressed. In both materials an excess of carriers of relatively larger magnetic moments appears in dilute solutions than in concentrated ones. The results obtained for a solution of potassium ferricyanide differed from the earlier measurements of Collet.  相似文献   

7.
We report remarkable differences in the 1H nuclear magnetic relaxation dispersion data (NMRD) between water and other common aprotic solvents such as acetone when in contact with high surface area calibrated microporous chromatographic silica glasses that contain trace paramagnetic impurities located at or close to the pore surface. All these differences have been related to the particular chemical behaviors and dynamics of these liquids at the pore surface. We apply this technique to probe the structure and dynamics of water and oil at the surface of calibrated macroporous systems, where similar surface dynamics effects have been observed. This technique is also applied to follow the first hydration stage of a white cement-paste. Last, we present an analysis of the magnetic field dependence of 1H nuclear relaxation data to exhibit the microporosity of ultra high performance concretes.  相似文献   

8.
The docking or polymerization of globular proteins is demonstrated to cause changes in proton NMR spin-lattice (T1) relaxation times. Studies on solutions of lysozyme, bovine serum albumin, actin, and tubulin are used to demonstrate that two mechanisms account for the observed changes in T1. Polymerization displaces the hydration water sheath surrounding globular proteins in solution that causes an increase in T1. Polymerization also slows the average tumbling rate of the proteins, which typically causes a contrary decrease in T1. The crystallization reaction of lysozyme in sodium chloride solution further demonstrates that the "effective" molecular weight can either decrease or increase T1 depending on how much the protein is slowed. The displacement of hydration water increases T1 because it speeds up the mean motional state of water in the solution. Macromolecular docking typically decreases T1 because it slows the mean motional state of the solute molecules. Cross-relaxation between the proteins and bound water provides the mechanism that allows macromolecular motion to influence the relaxation rate of the solvent. Fast chemical exchange between bound, structured, and bulk water accounts for monoexponential spin-lattice relaxation. Thus the spin-lattice relaxation rate of water in protein solutions is a complex reflection of the motional properties of all the molecules present containing proton magnetic dipoles. It is expected, as a result, that the characteristic relaxation times of tissues will reflect the influence of polymerization changes related to cellular activities.  相似文献   

9.
利用差示扫描量热仪研究了5种高浓度丙三醇水溶液(60%、70%、80%、90%、100%)的玻璃化转变行为,以考察水分含量和升降温速率对其玻璃化转变行为和结构松弛参数的影响.采用4种线性升降温速率(10、15、20、25K/min)获得玻璃化转变的相关参数.利用GordonTaylor方程对玻璃化转变温度的分析结果表明,水对丙三醇增塑常数的计算结果与升降温速率和玻璃化转变温度的读取方法有很大关系.玻璃化转变过程的比热容变化不仅随水分含量的增加而增加,而且与升降温速率也有一定的依赖关系.结构松弛活化能的计算结果表明,随体系水分含量的增加,体系的结构松弛活化能和动力学脆度都逐渐降低.随水分含量的变化,热力学脆度和动力学脆度表现出相反的变化趋势.  相似文献   

10.
We propose a new NMR method to measure and follow the evolution of the surface specific area, Sp, of a porous cement-based material. This method, that does not require any preliminary drying process, uses nuclear magnetic relaxation dispersion (NMRD), the measurement of spin-lattice relaxation rate as a function of magnetic field strength or nuclear Larmor frequency. The method is applied for three different mortars samples prepared by mixing cement, sand, silica fume, water and superplasticizer with a water to cement ratio w/c=0.25, 0.38 and 0.65, respectively. The evolution of Sp grows linearly with the degree of advancement of chemical reactions measured by thermal heating and we evidence two relaxation processes independent of the w/c ratio.  相似文献   

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