Structural characterization of nanofiber silk produced by embiopterans (webspinners)

Embiopterans produce silken galleries and sheets using exceptionally fine silk fibers in which they live and breed. In this study, we use electron microscopy (EM), Fourier-transform infrared (FT-IR) spectroscopy, wide angle X-ray diffraction (WAXD) and solid-state nuclear magnetic resonance (ssNMR) techniques to elucidate the molecular level protein structure of webspinner (embiid) silks. Silks from two species Antipaluria urichi and Aposthonia ceylonica are studied in this work. Electron microscopy images show that the fibers are about 90–100 nm in diameter, making webspinner silks among the finest of all known animal silks. Structural studies reveal that the silk protein core is dominated by β-sheet structures, and that the protein core is coated with a hydrophobic alkane-rich surface coating. FTIR spectra of native embiid silk shows characteristic alkane CH2 stretchings near 2800–2900 cm−1, which decrease approximately 50% after washing the silk with 2 : 1 CHCl3 : MeOH. Furthermore, 13C ssNMR data shows a significant CH2 resonance that is strongly affected by the presence of water, supporting the idea that the silk fibers are coated with a hydrocarbon-rich layer. Such a layer is likely used to protect the colonies from rain. FTIR data also suggests that embiid silks are dominated by β-sheet secondary structures similar to spider and silkworm silk fibers. NMR data confirms the presence of β-sheet nanostructures dominated by serine-rich repetitive regions. A deconvolution of the serine Cβ NMR resonance reveals that approximately 70% of all seryl residues exist in a β-sheet structure. This is consistent with WAXD results that suggest webspinner silks are 70% crystalline, which is the highest crystalline fraction reported for any animal silks. The work presented here provides a molecular level structural picture of silk fibers produced by webspinners

Organic salt composition of pressure sensitive adhesives produced by spiders

Natural glues offer great potential as bio-inspired solutions to problems associated with the performance of synthetic adhesives. Spider viscous glues are elastic pressure sensitive adhesives (PSAs) that physically adhere to surfaces on contact across a range of environmental conditions. Extracting useful components from these secretions remains a challenge that can be met by the comparative analyses of functional analogues. Here we used 1H NMR spectroscopy and mass spectrometry to ascertain the organic salt compositions of the PSAs of four different species of Australian spiders belonging to two lineages that independently acquired aqueous gluey secretions: the St Andrew’s cross (Argiope keyserlingi), the redback (Latrodectus hasselti), the false widow (Steatoda grossa), and the daddy long-legs spider (Pholcus phalangiodes). The PSAs from each of these spiders contained similar organic salts, albeit in variable concentrations. The adhesives of the false widow and daddy long-legs spider had mixtures of only a few components, of which betaine predominated, while the PSAs of the other spiders predominantly contained small organic acids such as GABA/GABA-amide, isethionate, and choline salts. Our results suggest that the PSA composition of spiders is likely to be influenced more by environmental factors than evolutionary history and are guided by common principles. Our findings could be valuable for facilitating the design of more sustainable synthetic glues

Molecular Dynamics of Spider Dragline Silk Fiber Investigated by ²H MAS NMR

The molecular dynamics of the proteins that comprise spider dragline silk were investigated with solid-state ²H magic angle spinning (MAS) NMR line shape and spin–lattice relaxation time (<i>T</i>₁) analysis. The experiments were performed on ²H/¹³C/¹⁵N-enriched N. clavipes dragline silk fibers. The silk protein side-chain and backbone dynamics were probed for Ala-rich regions (β-sheet and 3₁-helical domains) in both native (dry) and supercontracted (wet) spider silk. In native (dry) silk fibers, the side chains in all Ala containing regions undergo similar fast methyl rotations (>10⁹ s^–1), while the backbone remains essentially static (<10² s^–1). When the silk is wet and supercontracted, the presence of water initiates fast side-chain and backbone motions for a fraction of the β-sheet region and 3₁-helicies. β-Sheet subregion 1 ascribed to the poly­(Ala) core exhibits slower dynamics, while β-sheet subregion 2 present in the interfacial, primarily poly­(Gly-Ala) region that links the β-sheets to disordered 3₁-helical motifs, exhibits faster motions when the silk is supercontracted. Particularly notable is the observation of microsecond backbone motions for β-sheet subregion 2 and 3₁-helicies. It is proposed that these microsecond backbone motions lead to hydrogen-bond disruption in β-sheet subregion 2 and helps to explain the decrease in silk stiffness when the silk is wet and supercontracted. In addition, water mobilizes and softens 3₁-helical motifs, contributing to the increased extensibility observed when the silk is in a supercontracted state. The present study provides critical insight into the supercontraction mechanism and corresponding changes in mechanical properties observed for spider dragline silks

Effects of Different Post-Spin Stretching Conditions on the Mechanical Properties of Synthetic Spider Silk Fibers

Spider silk is a biomaterial with impressive mechanical properties, resulting in various potential applications. Recent research has focused on producing synthetic spider silk fibers with the same mechanical properties as the native fibers. For this study, three proteins based on the Argiope aurantia Major ampullate Spidroin 2 consensus repeat sequence were expressed, purified and spun into fibers. A number of post-spin draw conditions were tested to determine the effect of each condition on the mechanical properties of the fiber. In all cases, post-spin stretching improved the mechanical properties of the fibers. Aqueous isopropanol was the most effective solution for increasing extensibility, while other solutions worked best for each fiber type for increasing tensile strength. The strain values of the stretched fibers correlated with the length of the proline-rich protein sequence. Structural analysis, including X-ray diffraction and Raman spectroscopy, showed surprisingly little change in the initial as-spun fibers compared with the post-spin stretched fibers

Bimodal phase percolation model for the structure of Ge-Se glasses and the existence of the intermediate phase

International audienceA detailed nuclear magnetic resonance and Raman study of GexSe1−x glasses indicate that the glass structure is composed of intertwined microdomains of GeSe2 and Sen. Static nuclear magnetic resonance spectra of glasses ranging from 0≤x≤1/3 reveal the absence of Ge-Se-Se fragments in the structure. High temperature nuclear magnetic resonance showing considerable line narrowing confirms this observation. More importantly, the fraction of Se-Se-Se obtained by integration of nuclear magnetic resonance lines matches closely the percentage predicted for a bimodal phase model and is not consistent with the existence of Ge-Se-Se fragments. Raman spectra collected on the same glass also confirm the existence of GeSe2 domains up to high selenium concentrations. The mobility of the Sen phase observed at high temperature while the GeSe2 phase remains rigid is consistent with their respective underconstrained and overconstrained structural nature. The proposed bimodal phase percolation model is consistent with the original Phillips and Thorpe theory however it is clearly at odds with the intermediate phase model which predicts large amounts of Ge-Se-Se fragments in the structure. A calorimetric study performed over a wide range of cooling/heating rates shows a narrow composition dependence centered at ⟨r⟩=2.4 in contrast with the wide reversibility window observed by Modulated Differential Scanning Calorimetry. This suggests that the observation of the reversibility window associated with the intermediate phase in Ge-Se glasses could be an experimental artifact resulting from the use of a single modulation frequency

Inducing β-Sheets Formation in Synthetic Spider Silk Fibers by Aqueous Post-Spin Stretching

As a promising biomaterial with numerous potential applications, various types of synthetic spider silk fibers have been produced and studied in an effort to produce man-made fibers with mechanical and physical properties comparable to those of native spider silk. In this study, two recombinant proteins based on Nephila clavipes Major ampullate Spidroin 1 (MaSp1) consensus repeat sequence were expressed and spun into fibers. Mechanical test results showed that fiber spun from the higher molecular weight protein had better overall mechanical properties (70 KD versus 46 KD), whereas postspin stretch treatment in water helped increase fiber tensile strength significantly. Carbon-13 solid-state NMR studies of those fibers further revealed that the postspin stretch in water promoted protein molecule rearrangement and the formation of β-sheets in the polyalanine region of the silk. The rearrangement correlated with improved fiber mechanical properties and indicated that postspin stretch is key to helping the spider silk proteins in the fiber form correct secondary structures, leading to better quality fibers