Study of protein conformation and orientation in silkworm and spider silk fibers using Raman microspectroscopy

被引:278
作者
Rousseau, ME
Lefèvre, T
Beaulieu, L
Asakura, T
Pézolet, M
机构
[1] Univ Laval, CERSIM, CREFSIP, Dept Chim, Quebec City, PQ G1K 7P4, Canada
[2] Tokyo Univ Agr & Technol, Dept Biotechnol, Fuchu, Tokyo 183, Japan
关键词
D O I
10.1021/bm049717V
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 <P-2> and <P-4> of the orientation distribution function from intensity ratios of polarized Raman spectra. The equations allowing the calculation of <P-2> and <P-4> 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 <P-2> and <P-4> 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 <P-2> and <P-4> 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 P,) 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 32degrees and 40degrees 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.
引用
收藏
页码:2247 / 2257
页数:11
相关论文
共 75 条
[11]   Conformation transition kinetics of regenerated Bombyx mori silk fibroin membrane monitored by time-resolved FTIR spectroscopy [J].
Chen, X ;
Shao, ZZ ;
Marinkovic, NS ;
Miller, LM ;
Zhou, P ;
Chance, MR .
BIOPHYSICAL CHEMISTRY, 2001, 89 (01) :25-34
[12]   MOLECULAR-ORIENTATION OF HIGH-DENSITY POLYETHYLENE FIBERS CHARACTERIZED BY POLARIZED RAMAN-SPECTROSCOPY [J].
CITRA, MJ ;
CHASE, DB ;
IKEDA, RM ;
GARDNER, KH .
MACROMOLECULES, 1995, 28 (11) :4007-4012
[13]   VIBRATIONAL ANALYSIS OF PEPTIDES, POLYPEPTIDES, AND PROTEINS .11. BETA-POLY(L-ALANINE) AND ITS N-DEUTERATED DERIVATIVE [J].
DWIVEDI, AM ;
KRIMM, S .
MACROMOLECULES, 1982, 15 (01) :186-193
[14]   RAMAN-SPECTROSCOPIC STUDIES OF SILK [J].
EDWARDS, HGM ;
FARWELL, DW .
JOURNAL OF RAMAN SPECTROSCOPY, 1995, 26 (8-9) :901-909
[15]  
Fraser R. D. B., 1973, CONFORMATION FIBROUS, P94
[16]  
Freddi G, 1997, J POLYM SCI POL PHYS, V35, P841, DOI 10.1002/(SICI)1099-0488(19970415)35:5<841::AID-POLB13>3.0.CO
[17]  
2-A
[18]  
FRUSHOUR BG, 1976, J MACROMOL SCI R M C, VC 15, P29
[19]   RAMAN SPECTROSCOPIC STUDY OF TROPOMYOSIN DENATURATION [J].
FRUSHOUR, BG ;
KOENIG, JL .
BIOPOLYMERS, 1974, 13 (09) :1809-1819
[20]  
GILLESPIE DB, 1994, ACS SYM SER, V544, P155