Conformational transition and liquid crystalline state of regenerated silk fibroin in water
✍ Scribed by Xin-Gui Li; Li-Ya Wu; Mei-Rong Huang; Hui-Li Shao; Xue-Chao Hu
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2008
- Tongue
- English
- Weight
- 510 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The conformational transition of molecular chains of regenerated silk fibroin (SF) aqueous solution is systematically investigated by circular dichroism, Raman, IR, and UV–vis spectroscopies. It is found that an initial random coil conformation of the SF can be readily changed into an ordered β‐sheet structure by optimizing the solution conditions, such as the SF concentration, pH, temperature, or metal‐ion content. Circular dichroic spectra quantitatively confirm a steadily decreased content of the random coil conformation but a significantly increased β‐sheet content after an ultrasonic or extruding treatment. Furthermore, the extrusion is more powerful to achieve high β‐sheet content than the ultrasonic. It is interesting that the polarized optical micrographs of the SF aqueous solution extruded by injection illustrate the formation and existence of liquid crystalline state. A study of extrusion in vitro could be used as a model system to understand the natural silk spinning process in silkworm. © 2007 Wiley Periodicals, Inc. Biopolymers 89: 497–505, 2008.
This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at [email protected]
📜 SIMILAR VOLUMES
The conformational transformation of a 30-residue peptide H(Ala-Gly-Ser-Gly-Ala-Gly) 5 OH, i.e., (AGSGAG) 5 , extracted from highly crystalline region of Bombyx mori (B. mori) silk fibroin was described by using the high resolution solid state 13 C NMR, and CD spectroscopies. Based on the conformati
The conformation around the bond of the alkyl spacer of a,u-bis[(4,4@-cyanobiphenylyl)oxy] C e ÈC e@ decane (CBA-10) was evaluated in the solid and liquid crystalline states through the detection of the dipolar interaction between and CBA-10 13C-labelled in the d position of the alkyl spacer was pr
## Abstract The conformation of the ethoxy tail flanking the cyanobiphenyl core has been studied in the liquid‐crystalline phase as well as in the isotropic solution. In solution, the vicinal coupling constant ^3^J~CH~ for the moiety C^ph^OCH (C^ph^: phenyl carbon) provided the information regardi