Imai Takashi, Ohyama Shusaku, Kovalenko Andriy, Hirata Fumio
Department of Bioscience and Bioinformatics, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan.
Protein Sci. 2007 Sep;16(9):1927-33. doi: 10.1110/ps.072909007. Epub 2007 Jul 27.
The partial molar volume (PMV) change associated with the pressure-induced structural transition of ubiquitin is analyzed by the three-dimensional reference interaction site model (3D-RISM) theory of molecular solvation. The theory predicts that the PMV decreases upon the structural transition, which is consistent with the experimental observation. The volume decomposition analysis demonstrates that the PMV reduction is primarily caused by the decrease in the volume of structural voids in the protein, which is partially canceled by the volume expansion due to the hydration effects. It is found from further analysis that the PMV reduction is ascribed substantially to the penetration of water molecules into a specific part of the protein. Based on the thermodynamic relation, this result implies that the water penetration causes the pressure-induced structural transition. It supports the water penetration model of pressure denaturation of proteins proposed earlier.
利用分子溶剂化的三维参考相互作用位点模型(3D-RISM)理论,分析了与泛素压力诱导结构转变相关的偏摩尔体积(PMV)变化。该理论预测,结构转变时PMV会减小,这与实验观察结果一致。体积分解分析表明,PMV的减小主要是由蛋白质中结构空隙体积的减小引起的,而由于水合作用导致的体积膨胀会部分抵消这种减小。进一步分析发现,PMV的减小主要归因于水分子渗透到蛋白质的特定部位。基于热力学关系,这一结果意味着水的渗透导致了压力诱导的结构转变。它支持了早期提出的蛋白质压力变性的水渗透模型。