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Characterization by Raman Microspectroscopy of the Strain-Induced Conformational Transition in Fibroin Fibers from the Silkworm Samia cynthia ricini

机译:通过拉曼光谱表征的蚕桑蛋白丝蛋白的纤维蛋白纤维中的应变诱导的构象转变。

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Raman microspectroscopy has been used to quantitatively study the effect of a mechanical deformation on the conformation and orientation of Samia cynthia ricini (S.c.ricini) silk fibroin.Samples were obtained from the aqueous solution stored in the silk gland and stretched at draw ratios (lambda) ranging from 0 to 11.Using an appropriate band decomposition procedure,polarized and orientation-insensitive spectra have been analyzed to determine order parameters and the content of secondary structures,respectively.The data unambiguously show that,in response to mechanical deformation,S.c.ricini fibroin undergoes a cooperative alpha-helix to beta-sheet conformational transition above a critical draw ratio of 4.The alpha-helix content decreases from 33 to 13% when lambda increases from 0 to 11,while the amount of beta-sheets increases from 15 to 37%.In comparison,cocoon silk is devoid of alpha-helical structure and always contains a larger amount of beta-sheets.Although the presence of isosbestic points in different spectral regions reveals that the conformational change induced by mechanical deformation is a two-state process,our results suggest that part of the glycine residues might be incorporated into beta-poly(alanine) structures.The beta-sheets are initially isotropically distributed and orient along the fiber axis as lambda increases,but do not reach the high level of orientation found in the cocoon fiber.The increase in the orientation level of the beta-sheets is found to be concomitant with the alpha->beta conformational conversion,whereas alpha-helices do not orient under the applied strain but are rather readily converted into beta-sheets.The components assigned to turns exhibit a small orientation perpendicular to the fiber axis in stretched samples,showing that,overall,the polypeptide chains are aligned along the stretching direction.Our results suggest that,in nature,factors other than stretching contribute to the optimization of the amount of beta-sheets and the high degree of orientation found in natural cocoon silk.
机译:拉曼光谱用于定量研究机械变形对Samia cynthia ricini(Scricini)丝素蛋白构象和取向的影响,样品是从储存在丝腺中的水溶液中获得的,并以拉伸比(λ)拉伸范围从0到11。使用适当的谱带分解程序,分别分析了偏振和取向不敏感的光谱以确定阶数参数和二级结构的含量。数据清楚地表明,响应于机械变形,Scricini丝素蛋白在超过4的临界拉伸比时经历从α-螺旋到β-折叠的构象过渡。当λ从0增加到11时,α-螺旋含量从33%降低到13%,而β-折叠的数量从15增加到13 37%。相比之下,茧丝缺乏α-螺旋结构,并且始终包含大量的β-折叠片。在不同光谱区域的最佳点表明,机械变形引起的构象变化是一个两态过程,我们的结果表明部分甘氨酸残基可能被掺入了β-聚丙氨酸结构中。β-折叠最初是各向同性的随着λ增加,沿纤维轴分布并沿纤维轴取向,但未达到茧纤维中的高取向水平。发现β-折叠的取向水平增加与α->β构象转化相伴,而α-螺旋在所施加的应变下不定向,而是很容易转化为β-折叠。分配给转体的成分在拉伸的样品中显示出垂直于纤维轴的小的定向,这表明多肽链总体上是对齐的我们的研究结果表明,本质上,除拉伸以外的其他因素也有助于优化β-折叠的数量天然茧丝具有很高的取向度。

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