Literature DB >> 16961312

Characterization by Raman microspectroscopy of the strain-induced conformational transition in fibroin fibers from the silkworm Samia cynthia ricini.

Marie-Eve Rousseau1, Lilyane Beaulieu, Thierry Lefèvre, Joanie Paradis, Tetsuo Asakura, Michel Pézolet.   

Abstract

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.

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Year:  2006        PMID: 16961312     DOI: 10.1021/bm060280w

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  14 in total

1.  Protein secondary structure and orientation in silk as revealed by Raman spectromicroscopy.

Authors:  Thierry Lefèvre; Marie-Eve Rousseau; Michel Pézolet
Journal:  Biophys J       Date:  2007-02-02       Impact factor: 4.033

2.  Assembly mechanism of recombinant spider silk proteins.

Authors:  S Rammensee; U Slotta; T Scheibel; A R Bausch
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-29       Impact factor: 11.205

3.  Polarized Raman Spectroscopy for Determining the Orientation of di-D-phenylalanine Molecules in a Nanotube.

Authors:  Valentin Sereda; Nicole M Ralbovsky; Milana C Vasudev; Rajesh R Naik; Igor K Lednev
Journal:  J Raman Spectrosc       Date:  2016-02-17       Impact factor: 3.133

4.  Characterization of nanofibers for tissue engineering: Chemical mapping by Confocal Raman microscopy.

Authors:  Anna Sharikova; Zahraa I Foraida; Lauren Sfakis; Lubna Peerzada; Melinda Larsen; James Castracane; Alexander Khmaladze
Journal:  Spectrochim Acta A Mol Biomol Spectrosc       Date:  2019-10-19       Impact factor: 4.098

5.  Identification of Wet-Spinning and Post-Spin Stretching Methods Amenable to Recombinant Spider Aciniform Silk.

Authors:  Nathan Weatherbee-Martin; Lingling Xu; Andre Hupe; Laurent Kreplak; Douglas S Fudge; Xiang-Qin Liu; Jan K Rainey
Journal:  Biomacromolecules       Date:  2016-07-20       Impact factor: 6.988

6.  Correlation between protein secondary structure and mechanical performance for the ultra-tough dragline silk of Darwin's bark spider.

Authors:  K Zin Htut; Angela M Alicea-Serrano; Saranshu Singla; Ingi Agnarsson; Jessica E Garb; Matjaž Kuntner; Matjaž Gregorič; Robert A Haney; Mohammad Marhabaie; Todd A Blackledge; Ali Dhinojwala
Journal:  J R Soc Interface       Date:  2021-06-16       Impact factor: 4.293

7.  Spider wrapping silk fibre architecture arising from its modular soluble protein precursor.

Authors:  Marie-Laurence Tremblay; Lingling Xu; Thierry Lefèvre; Muzaddid Sarker; Kathleen E Orrell; Jérémie Leclerc; Qing Meng; Michel Pézolet; Michèle Auger; Xiang-Qin Liu; Jan K Rainey
Journal:  Sci Rep       Date:  2015-06-26       Impact factor: 4.379

8.  Structure Water-Solubility Relationship in α-Helix-Rich Films Cast from Aqueous and 1,1,1,3,3,3-Hexafluoro-2-Propanol Solutions of S. c. ricini Silk Fibroin.

Authors:  Kelvin O Moseti; Taiyo Yoshioka; Tsunenori Kameda; Yasumoto Nakazawa
Journal:  Molecules       Date:  2019-10-31       Impact factor: 4.411

9.  Polarized Raman anisotropic response of collagen in tendon: towards 3D orientation mapping of collagen in tissues.

Authors:  Leonardo Galvis; John W C Dunlop; Georg Duda; Peter Fratzl; Admir Masic
Journal:  PLoS One       Date:  2013-05-15       Impact factor: 3.240

10.  Identification and classification of silks using infrared spectroscopy.

Authors:  Maxime Boulet-Audet; Fritz Vollrath; Chris Holland
Journal:  J Exp Biol       Date:  2015-09-07       Impact factor: 3.312

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