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Observations of 3 nm Silk Nanofibrils Exfoliated from Natural Silkworm Silk Fibers AITranslate

Harvard University; Tufts University; Tsinghua University; Tsinghua University;Nanophotonics Research Division, CAS Center for Excellence in Nanoscience;Nanophotonics Research Division, CAS Center for Excellence in Nanoscience; Harvard University; Tufts University; Massachusetts Institute of Technology; Tsinghua University
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Publisher: ACS
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Abstract AITranslate

Silk fibers are one of the most attractive natural materials that exhibit enchanting luster and superior mechanical properties. Exploring the unique hierarchical architecture structures of natural silk fibers is the basis to understanding these unique properties. Here, we report observations of 3.1 ± 0.8 nm silk nanofibrils and 3.7 ± 0.9 Å silk molecule chains exfoliated from natural silkworm silk fibers. Interestingly, the individual nanofibrils and protein chains show periodic diameters fluctuating along their axes. We further find that the thicker regions are relatively softer and the thinner regions are stiffer, and these can be assigned to alternatively distributed α-helix and β-sheet domains, respectively. Based on these observations, we proposed a refined structure model of natural silk, which ranges from the molecular level to the fiber scale. These findings provide new opportunities to understand and exploit the unique structure–property relationships found in natural silk fibers, including inspiring the design of new artificial materials.

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DOI:https://doi.org/10.1021/acsmaterialslett.9b00461

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Citation Information:

Silk fibers are one of the most attractive natural materials that exhibit enchanting luster and superior mechanical properties. Exploring the unique hierarchical architecture structures of natural silk fibers is the basis to understanding these unique properties. Here, we report observations of 3.1 ± 0.8 nm silk nanofibrils and 3.7 ± 0.9 Å silk molecule chains exfoliated from natural silkworm silk fibers. Interestingly, the individual nanofibrils and protein chains show periodic diameters fluctuating along their axes. We further find that the thicker regions are relatively softer and the thinner regions are stiffer, and these can be assigned to alternatively distributed α-helix and β-sheet domains, respectively. Based on these observations, we proposed a refined structure model of natural silk, which ranges from the molecular level to the fiber scale. These findings provide new opportunities to understand and exploit the unique structure–property relationships found in natural silk fibers, including inspiring the design of new artificial materials.

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GB/T 7714-2015 [1] Qi Wang, Shengjie Ling, Quanzhou Yao, et al. ACS Materials Letters, 2020(2). DOI:10.1021/acsmaterialslett.9b00461.
MLA [1] Qi Wang, et al., ACS Materials Letters, no. 2, 2020, https://doi.org/10.1021/acsmaterialslett.9b00461.
APA [1] Qi Wang, Shengjie Ling, Quanzhou Yao, Qunyang Li, Debo Hu, Qing Dai, David A. Weitz, David L. Kaplan, Markus J. Buehler, & Yingying Zhang. (2020). ACS Materials Letters(2). https://doi.org/10.1021/acsmaterialslett.9b00461
IEEE [1] Qi Wang, Shengjie Ling, Quanzhou Yao, Qunyang Li, Debo Hu, Qing Dai, David A. Weitz, David L. Kaplan, Markus J. Buehler, and Yingying Zhang, ACS Materials Letters, no. 2, 2020, doi: 10.1021/acsmaterialslett.9b00461.