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利用质子和氘核纵向弛豫时间对蛋白质溶液和组织中的流体动力学效应及交叉弛豫进行定量研究。

Quantitative studies of hydrodynamic effects and cross-relaxation in protein solutions and tissues with proton and deuteron longitudinal relaxation times.

作者信息

Zhong J H, Gore J C, Armitage I M

机构信息

Department of Diagnostic Radiology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Magn Reson Med. 1990 Feb;13(2):192-203. doi: 10.1002/mrm.1910130203.

Abstract

Longitudinal relaxation times T1 of water protons were measured in 5% protein solutions at different static magnetic fields (0.47, 2, and 7 T), for proteins with molecular weight ranging between 1.4 and 480 kDa and in solvents of varying degrees of deuteration. T1 values were also obtained for rat liver soaked with Krebs-Ringer solutions of varying degrees of deuteration at the above fields. For the samples containing D2O, T1 for deuterium was also measured at fields 2 and 7 T. The deuterium measurements were used to estimate water rotational correlation times which were in turn used to estimate the contribution of so-called "hydrodynamic effects" of macromolecules to proton relaxation. The proton relaxation rates at full deuteration were compared with those in protonated solvent (water) to obtain a second, direct measurement of this effect. Both measurements provide quantitation of the hydrodynamic effects, free from the contributions of other effects that are transparent to deuteration, and results from both measurements agree with each other reasonably well. The cross-relaxation rate between solute and solvent protons, and the contribution of paramagnetic impurities in the samples were also obtained from the proton T1 studies. The experimental results show that the hydrodynamic effects (intramolecular and intermolecular water-water interactions) are about the same magnitude in all the proteins studied as well as in rat liver. However, the cross-relaxation rate generally increases with increasing protein molecular weight. Measurements in soaked rat liver indicate that the cross-relaxation rate per unit mass of solute is much higher in tissues than in simple solutions of proteins of similar mean molecular weight. The results challenge the prevailing concept that the relaxation properties of biological tissues may be treated as a simple superposition of the properties of their constituents.

摘要

在不同的静磁场(0.47、2和7特斯拉)下,对分子量在1.4至480 kDa之间的蛋白质以及不同氘化程度的溶剂中的5%蛋白质溶液,测量了水质子的纵向弛豫时间T1。在上述磁场下,还对用不同氘化程度的 Krebs-Ringer 溶液浸泡的大鼠肝脏进行了T1值测量。对于含有重水(D2O)的样品,还在2和7特斯拉的磁场下测量了氘的T1。氘的测量用于估计水的旋转相关时间,进而用于估计大分子所谓的“流体动力学效应”对质子弛豫的贡献。将完全氘化时的质子弛豫率与质子化溶剂(水)中的弛豫率进行比较,以获得对该效应的第二种直接测量。两种测量都提供了流体动力学效应的定量结果,不受其他对氘化透明的效应的影响,并且两种测量的结果相当吻合。溶质与溶剂质子之间的交叉弛豫率以及样品中顺磁性杂质的贡献也从质子T1研究中获得。实验结果表明,在所研究的所有蛋白质以及大鼠肝脏中,流体动力学效应(分子内和分子间的水 - 水相互作用)的大小大致相同。然而,交叉弛豫率通常随着蛋白质分子量的增加而增加。浸泡大鼠肝脏的测量表明,单位质量溶质的交叉弛豫率在组织中比在平均分子量相似的简单蛋白质溶液中要高得多。这些结果挑战了普遍的观念,即生物组织的弛豫特性可以被视为其成分特性的简单叠加。

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