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同源二糖对生物大分子的生物保护作用。

Bio-protective effects of homologous disaccharides on biological macromolecules.

机构信息

Department of Physics, University of Messina, Viale Ferdinando Stagno D'Alcontres no. 31, P.O. Box 55, 98166 S. Agata, Messina, Italy.

出版信息

Eur Biophys J. 2012 Apr;41(4):361-7. doi: 10.1007/s00249-011-0760-x. Epub 2011 Oct 30.

Abstract

In this contribution the effects of the homologous disaccharides trehalose and sucrose on both water and hydrated lysozyme dynamics are considered by determining the mean square displacement (MSD) from elastic incoherent neutron scattering (EINS) experiments. The self-distribution function (SDF) procedure is applied to the data collected, by use of IN13 and IN10 spectrometers (Institute Laue Langevin, France), on trehalose and sucrose aqueous mixtures (at a concentration corresponding to 19 water molecules per disaccharide molecule), and on dry and hydrated (H(2)O and D(2)O) lysozyme also in the presence of the disaccharides. As a result, above the glass transition temperature of water, the MSD of the water-trehalose system is lower than that of the water-sucrose system. This result suggests that the hydrogen-bond network of the water-trehalose system is stronger than that of the water-sucrose system. Furthermore, by taking into account instrumental resolution effects it was found that the system relaxation time of the water-trehalose system is longer than that of the water-sucrose system, and the system relaxation time of the protein in a hydrated environment in the presence of disaccharides increases sensitively. These results explain the higher bioprotectant effectiveness of trehalose. Finally, the partial MSDs of sucrose/water and trehalose/water have been evaluated. It clearly emerges from the analysis that these are almost equivalent in the low-Q domain (0-1.7 Å(-1)) but differ substantially in the high-Q range (1.7-4 Å(-1)). These findings reveal that the lower structural sensitivity of trehalose to thermal changes is connected with the local spatial scale.

摘要

在这项工作中,通过测定弹性非相干中子散射(EINS)实验中的均方位移(MSD),研究了同源二糖海藻糖和蔗糖对水和水合溶菌酶动力学的影响。使用 IN13 和 IN10 光谱仪(法国劳厄-朗之万研究所),对海藻糖和蔗糖水溶液(对应于每个二糖分子有 19 个水分子的浓度)以及干燥和水合(H2O 和 D2O)溶菌酶(同时存在二糖)的实验数据,采用自分布函数(SDF)方法进行了分析。结果表明,在高于水的玻璃化转变温度时,水-海藻糖体系的 MSD 低于水-蔗糖体系。这一结果表明,水-海藻糖体系的氢键网络强于水-蔗糖体系。此外,通过考虑仪器分辨率的影响,发现水-海藻糖体系的体系弛豫时间长于水-蔗糖体系,并且在存在二糖的水合环境中蛋白质的体系弛豫时间明显增加。这些结果解释了海藻糖具有更高的生物保护效果的原因。最后,还评估了蔗糖/水和海藻糖/水的部分 MSD。分析结果清楚地表明,在低 Q 域(0-1.7 Å-1)内,它们几乎相等,但在高 Q 域(1.7-4 Å-1)内则有很大差异。这些发现表明,海藻糖对热变化的结构敏感性较低与局部空间尺度有关。

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