Applied Spectroscopy · 2015 · 10 citations · 66 references
Natural SciencesMaterials EngineeringMaterials ScienceBiomaterialsPolymer ChemistryPolymer MaterialsDeformation MechanismsFiber PropertiesFibrous ProteinsPolymer PhysicsSoft MaterialsDeformationFiber SpinningLinear DichroismMechanical Properties Of Fibrous ProteinsMechanical Stress ResponseNatural Fiber MaterialsPolymer Amorphous Phase BehaviorStrain-induced Transformation
To better understand the effect of mechanical stress during the spinning of silk, the protein orientation and conformation of Bombyx mori regenerated silk fibroin (RSF) films have been studied as a function of deformation in a static mode or in real time by tensile-Raman experiments and polarization modulation infrared linear dichroism (PM-IRLD), respectively. The data show that either for step-by-step or continuous stretching, elongation induces the progressive formation of β-sheets that align along the drawing axis, in particular above a draw ratio of ~2. The formation of β-sheets begins before their alignment during a continuous drawing. Unordered chains were, however, never found to be oriented, which explains the very low level of orientation of the amorphous phase of the natural fiber. Stress-perturbed unordered chains readily convert into β-sheets, the strain-induced transformation following a two-state process. The final level of orientation and β-sheet content are lower than those found in the native fiber, indicating that various parameters have to be optimized in order to implement a spinning process as efficient as the natural one. Finally, during the stress relaxation period in a step-by-step drawing, there is essentially no change of the content and orientation of the β-sheets, suggesting that only unordered structures tend to reorganize.
66
Spider Silk Fibers Spun from Soluble Recombinant Silk Produced in Mammalian Cells
Anthoula Lazaris, Steven Arcidiacono, Yue Huang et al. · Science · 2002 · 748 citations
Water-insoluble silk films with silk I structure
Qiang Lü, Xiao Hu, Xiaoqin Wang et al. · Acta Biomaterialia · 2009 · 642 citations
Natural Sciences, Materials Engineering, Materials Science +5
Self-assembly of spider silk proteins is controlled by a pH-sensitive relay
Glareh Askarieh, My Hedhammar, Kerstin Nordling et al. · Nature · 2010 · 463 citations
A conserved spider silk domain acts as a molecular switch that controls fibre assembly
Franz Hagn, Lukas Eisoldt, John G. Hardy et al. · Nature · 2010 · 445 citations · Full text