首页> 外文期刊>Biophysical Chemistry: An International Journal Devoted to the Physical Chemistry of Biological Phenomena >Conformation transition kinetics of regenerated Bombyx mori silk fibroin membrane monitored by time-resolved FTIR spectroscopy.
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Conformation transition kinetics of regenerated Bombyx mori silk fibroin membrane monitored by time-resolved FTIR spectroscopy.

机译:通过时间分辨FTIR光谱监测再生家蚕丝素蛋白膜的构象转变动力学。

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摘要

The ethanol-induced conformation transition of regenerated Bombyx mori silk fibroin membrane from a poorly defined to the well ordered state was monitored by time-resolved Fourier transform infrared spectroscopy (FTIR) for the first time. From the analysis of FTIR difference spectra, taken on time scales as short as 6 s and up to 1 h after addition of ethanol, intensity vs. time plots of an increasing band at 1618 cm(-1) were observed indicating formation of a beta-sheet coincident with the loss of intensity of a band at 1668 cm(-1) indicating decreases of random coil and/or silk I structure. Both infrared markers were fitted with identical biphasic exponential decay functions, however, there was a clear burst phase occurring prior to the onset of the observed transitions. The conformation transition process is indicated to either proceed sequentially through (at least) two intermediate states that contain different levels of beta-sheet structure or to have parallel pathways of initial beta-sheet formation followed by a slower 'perfection' phase. The first observed process forms in a burst phase a few seconds after mixing (or even faster), prior to the collection of the first spectrum at 6 s. The second observed process occurs with a time constant of approximately 0.5 min, the intermediate present at this stage then continues with a time constant of 5.5 min completing the observed formation of the beta-sheet. The conformation transition of this slower intermediate is not only indicated by an analysis of the kinetics of the random coil and beta-sheet-specific bands discussed above, it roughly coincides with the appearance of an additional infrared marker at 1695 cm(-1), which may be a marker for beta-sheet structure specific to the formation of the perfected structure. The conformation transition of this protein analyzed by infrared spectroscopy provides insight into a part of the fascinating process of cocoon formation in B. mori.
机译:首次通过时间分辨傅立叶变换红外光谱(FTIR)监测了乙醇诱导的家蚕丝素蛋白膜从不清晰状态到有序状态的构象转变。通过对FTIR差异光谱的分析,在添加乙醇后短至6 s直至1 h的时间范围内,观察到1618 cm(-1)处增加的谱带强度与时间的关系图,表明形成了β -薄片与在1668 cm(-1)处的条带强度损失一致,表明无规卷曲和/或丝I结构减少。两种红外标记都具有相同的双相指数衰减函数,但是,在观察到的跃迁开始之前出现了明显的猝发相。构象转变过程被指示为依次通过(至少)包含不同水平的β-折叠结构的两个中间状态进行,或具有初始的β-折叠形成的平行途径,随后是较慢的“完美”阶段。观察到的第一个过程是在混合后几秒钟(甚至更快),即在6 s处收集第一光谱之前的爆发阶段形成的。第二个观察到的过程以约0.5分钟的时间常数发生,然后在此阶段存在的中间体以5.5分钟的时间常数继续进行,从而完成了观察到的β-折叠的形成。较慢的中间体的构象转变不仅通过上述随机线圈和β-折叠特异性带的动力学分析来表明,而且还与1695 cm(-1)处出现的其他红外标记大致吻合,它可能是β-折叠结构特有的标记物,该β-折叠结构特异于形成完美的结构。通过红外光谱分析该蛋白的构象转变提供了对桑蚕中茧形成的迷人过程的一部分的了解。

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