Nishida Shinpei, Nada Tomokazu, Terazima Masahide
Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
Biophys J. 2005 Sep;89(3):2004-10. doi: 10.1529/biophysj.104.056762. Epub 2005 Jun 24.
Folding dynamics of reduced cytochrome c triggered by the laser-induced reduction method is investigated from a viewpoint of the intermolecular interaction change. Change of the diffusion coefficient of cytochrome c during the refolding process is traced in the time domain from the unfolded value to the native value continuously at various denaturant (guanidine hydrochloride (GdnHCl)) concentrations and temperatures. In the temperature range of 288 K-308 K and GdnHCl concentration range of 2.5 M-4.25 M, the diffusion change can be analyzed well by the two-state model consistently. It was found that the m(double dagger)-value and the activation energy of the transition state from the unfolded state for the hydrogen bonding network change are surprisingly similar to that for the local structural change around the heme group monitored by the fluorescence quenching experiment. This agreement suggests the existence of common or similar fundamental dynamics including water molecular movement to control the refolding dynamics. The nature of the transition state is discussed.
从分子间相互作用变化的角度研究了激光诱导还原法引发的还原型细胞色素c的折叠动力学。在不同变性剂(盐酸胍(GdnHCl))浓度和温度下,在时域中连续追踪细胞色素c在重折叠过程中扩散系数从展开值到天然值的变化。在288 K至308 K的温度范围和2.5 M至4.25 M的GdnHCl浓度范围内,双态模型能够很好地一致分析扩散变化。研究发现,氢键网络变化的展开态过渡态的m(双 dagger)值和活化能与通过荧光猝灭实验监测的血红素基团周围局部结构变化的情况惊人地相似。这种一致性表明存在包括水分子运动在内的共同或相似的基本动力学来控制重折叠动力学。讨论了过渡态的性质。