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家蚕丝蛋白的构象转变动力学

Conformation transition kinetics of Bombyx mori silk protein.

作者信息

Chen Xin, Shao Zhengzhong, Knight David P, Vollrath Fritz

机构信息

The Key Laboratory of Molecular Engineering of Polymers of MOE, Department of Macromolecular Science, Fudan University, Shanghai 200433, People's Republic of China.

出版信息

Proteins. 2007 Jul 1;68(1):223-31. doi: 10.1002/prot.21414.

Abstract

Time-resolved FTIR analysis was used to monitor the conformation transition induced by treating regenerated Bombyx mori silk fibroin films and solutions with different concentrations of ethanol. The resulting curves showing the kinetics of the transition for both films and fibroin solutions were influenced by the ethanol concentration. In addition, for silk fibroin solutions the protein concentration also had an effect on the kinetics. At low ethanol concentrations (for example, less than 40% v/v in the case of film), films and fibroin solutions showed a phase in which beta-sheets slowly formed at a rate dependent on the ethanol concentration. Reducing the concentration of the fibroin in solutions also slowed the formation of beta-sheets. These observations suggest that this phase represents a nucleation step. Such a nucleation phase was not seen in the conformation transition at ethanol concentrations > 40% in films or > 50% in silk fibroin solutions. Our results indicate that the ethanol-induced conformation transition of silk fibroin in films and solutions is a three-phase process. The first phase is the initiation of beta-sheet structure (nucleation), the second is a fast phase of beta-sheet growth while the third phase represents a slow perfection of previously formed beta-sheet structure. The nucleation step can be very fast or relatively slow, depending on factors that influence protein chain mobility and intermolecular hydrogen bond formation. The findings give support to the previous evidence that natural silk spinning in silkworms is nucleation-dependent, and that silkworms (like spiders) use concentrated silk protein solutions, and careful control of the pH value and metallic ion content of the processing environment to speed up the nucleation step to produce a rapid conformation transition to convert the water soluble spinning dope to a tough solid silk fiber.

摘要

采用时间分辨傅里叶变换红外光谱分析来监测用不同浓度乙醇处理再生家蚕丝素蛋白膜和溶液所诱导的构象转变。所得显示膜和丝素蛋白溶液转变动力学的曲线受乙醇浓度影响。此外,对于丝素蛋白溶液,蛋白质浓度也对动力学有影响。在低乙醇浓度下(例如,对于膜而言小于40% v/v),膜和丝素蛋白溶液呈现出一个阶段,其中β - 折叠以取决于乙醇浓度的速率缓慢形成。降低溶液中丝素蛋白的浓度也会减缓β - 折叠的形成。这些观察结果表明该阶段代表成核步骤。在膜中乙醇浓度>40%或丝素蛋白溶液中乙醇浓度>50%的构象转变中未观察到这样的成核阶段。我们的结果表明,乙醇诱导的膜和溶液中丝素蛋白的构象转变是一个三相过程。第一阶段是β - 折叠结构的起始(成核),第二阶段是β - 折叠快速生长阶段,而第三阶段代表先前形成的β - 折叠结构的缓慢完善。成核步骤可以非常快或相对较慢,这取决于影响蛋白质链流动性和分子间氢键形成的因素。这些发现支持了先前的证据,即家蚕中的天然丝纺丝是依赖成核的,并且家蚕(像蜘蛛一样)使用浓缩的丝蛋白溶液,并仔细控制加工环境的pH值和金属离子含量以加速成核步骤,从而产生快速的构象转变,将水溶性纺丝原液转化为坚韧的固体丝纤维。

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