Doctor of Philosophy (Ph.D.)
Hannes C Schniepp
Greg C Smith
Spider silk rivals the best synthetic materials in terms of strength and toughness. It is widely accepted that these properties arise from its internal structure. Despite extensive research, comprehensive experimental evidence of formation, morphology, mechanics, and the protein makeup of its internal structures are still limited, controversially discussed, or not studied at all. First, we report the complete mechanical decomposition of natural silk fibers from golden silk orb-weaver into ≈10 nm-diameter nanofibrils, the material’s apparent fundamental building blocks. Also, we produced nanofibrils of virtually identical morphology by triggering an intrinsic self-assembly mechanism of silk proteins. By analyzing protein self-assembly, we revealed independent physico-chemical fibrillation triggers which assemble proteins from stored precursors “at-will”. We also presented the first evidence-based structural model for spider silk fibers. According to our experimental work determining the nanofibrillar structure of spider silk, nanofibrils tend to align parallel to the fiber (axial) direction. The axially oriented nanofibrillar structure of spider silk gives rise to a significant mechanical anisotropy. This mechanical anisotropy is extremely difficult to quantify, especially for microscopically small materials such as spider silk, but has the potential to reveal important knowledge about the material’s structure-property relationships. We developed a novel method utilizing atomic force microscope (AFM) nanoindentations and finite element analysis (FEA) to characterize the mechanical anisotropy of such systems. We successfully used this method to measure the mechanics of nonfibrillar silk ribbons of the Chilean recluse spider, revealing the tensile and transverse elastic moduli as 9 GPa and 1 GPa, respectively, and the binding strength between silk nanofibrils as 159 ± 13 MPa. Furthermore, based on this binding strength, we derived the nanofibrils’ surface energy, as 37 mJ/m2, and also, found van der Waals forces play a decisive role in inter-fibrillar binding. Due to its versatility, our novel nanoindentation technique has many potential applications including early disease diagnostics, based on the mechanical properties of soft tissues. The impressive mechanical properties of spider silk nanofibrils can be further understood by studying their secondary protein structure, especially in the presence of fiber strain. We conducted strain-dependent Raman spectroscopy on nanofibrillar recluse silk and observed strain-dependent red shift in amide III protein band and strain-induced relative peak height changes in amide I/II/II bands. A wealth of knowledge about the behavior of protein secondary structures in the presence of fiber strain can be extracted by decomposing the amide bands into their subpeaks which correspond to each of the secondary protein structures. This extensive investigation of the structure, formation, and mechanics of nanofibrillar spider silk furthers our understanding of this exceptional material, and ultimately, leads us toward the realization of high-performance silk-based materials.
© The Author
Perera, Omaththage Dinidu Prabhath Nissanka, "Structure, Formation, And Mechanics Of Nanofibrillar Spider Silk" (2022). Dissertations, Theses, and Masters Projects. William & Mary. Paper 1686662831.
Available for download on Monday, January 20, 2025