Rousseau Marie-Eve, Lefèvre Thierry, Beaulieu Lilyane, Asakura Tetsuo, Pézolet Michel
Département de Chimie, CERSIM, CREFSIP, Université Laval, Pavillon Alexandre-Vachon, Québec (Québec) Canada G1K 7P4.
Biomacromolecules. 2004 Nov-Dec;5(6):2247-57. doi: 10.1021/bm049717v.
Raman microspectroscopy has been used for the first time to determine quantitatively the orientation of the beta-sheets in silk monofilaments from Bombyx mori and Samia cynthia ricini silkworms, and from the spider Nephila edulis. It is shown that, for systems with uniaxial symmetry such as silk, it is possible to determine the order parameters P2 and P4 of the orientation distribution function from intensity ratios of polarized Raman spectra. The equations allowing the calculation of P2 and P4 using polarized Raman microspectroscopy for a vibration with a cylindrical Raman tensor were first derived and then applied to the amide I band that is mostly due to the C=O stretching vibration of the peptide groups. The shape of the Raman tensor for the amide I vibration of the beta-sheets was determined from an isotropic film of Bombyx mori silk treated with methanol. For both the Bombyx mori and Samia cynthia ricini fibroin fibers, the values of P2 and P4 obtained are equal to -0.36 +/- 0.03 and 0.19 +/- 0.02, respectively, even though the two types of silkworm fibroins strongly differ in their primary sequences. For the Nephila edulis dragline silk, values of P2 and P4 of -0.32 +/- 0.02 and 0.13 +/- 0.02 were obtained, respectively. These results clearly indicate that the carbonyl groups are highly oriented perpendicular to the fiber axis and that the beta-sheets are oriented parallel to the fiber axis, in agreement with previous X-ray and NMR results. The most probable distribution of orientation was also calculated from the values of P2 and P4 using the information entropy theory. For the three types of silk, the beta-sheets are highly oriented parallel to the fiber axis. The orientation distributions of the beta-sheets are nearly Gaussian functions with a width of 32 degrees and 40 degrees for the silkworm fibroins and the spider dragline silk, respectively. In addition to these results, the comparison of the Raman spectra recorded for the different silk samples and the polarization dependence of several bands has allowed to clarify some important band assignments.
拉曼显微光谱首次被用于定量测定家蚕、蓖麻蚕和大腹园蛛单丝中β折叠的取向。结果表明,对于像丝绸这样具有单轴对称性的体系,通过偏振拉曼光谱的强度比可以确定取向分布函数的序参数P2和P4。首先推导了使用偏振拉曼显微光谱计算具有圆柱拉曼张量振动的P2和P4的方程,然后将其应用于主要由肽基团的C=O伸缩振动引起的酰胺I带。β折叠酰胺I振动的拉曼张量形状由用甲醇处理的家蚕丝各向同性薄膜确定。对于家蚕和蓖麻蚕的丝心蛋白纤维来说, 尽管这两种丝心蛋白的一级序列有很大差异,但得到的P2和P4值分别为-0.36±0.03和0.19±0.02。对于大腹园蛛的拖牵丝,得到的P2和P4值分别为-0.32±0.02和0.13±0.02。这些结果清楚地表明,羰基高度垂直于纤维轴取向,β折叠平行于纤维轴取向,这与之前的X射线和核磁共振结果一致。还利用信息熵理论从P2和P4值计算了最可能的取向分布。对于这三种类型的丝,β折叠高度平行于纤维轴取向。β折叠的取向分布近似为高斯函数,家蚕丝心蛋白和蜘蛛拖牵丝的半高宽分别为32°和40°。除了这些结果,对不同丝样品记录的拉曼光谱以及几个谱带的偏振依赖性进行比较,有助于明确一些重要的谱带归属。