journal article·2019-11

Scalable Spider‐Silk‐Like Supertough Fibers using a Pseudoprotein Polymer

Lin Gu, Yuanzhang Jiang, Jinlian Hu

Advanced Materials· Volume 31· Issue 48
Publisher page

Abstract

Abstract Spider silks are tougher than almost all other materials in the world and thus are considered ideal materials by scientists and the industry. Although there have been tremendous attempts to prepare fibers from genetically engineered spider‐silk proteins, it is still a very large challenge to artificially produce materials with a very high fracture energy, not to mention the high scaling‐up requirements because of the extremely low productivity and high cost levels. Here, a facile spider‐silk‐mimicking strategy is first reported for preparing scalable supertough fibers using the chemical synthesis route. Supertoughness (≈387 MJ m−3), more than twice the reported value of common spider dragline silk and comparable to the value of the toughest spider silk, the aciniform silk of Argiope trifasciata, is achieved by introducing β‐sheet crystals and α‐helical peptides simultaneously in a pseudoprotein polymer. The process opens up a very promising avenue for obtaining excellent spider fibers.
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Research context

OpenAlex topics: Silk-based biomaterials and applications · Antimicrobial Peptides and Activities · Biochemical and Structural Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Textiles and Clothing The Hong Kong Polytechnic University Hong Kong 999077 P. R. China

School of Chemical Engineering and Technology Sun Yat‐sen University Zhuhai 519082 P. R. China

Key Laboratory of Marine Materials and Related Technologies Zhejiang Key Laboratory of Marine Materials and Protective Technologies Ningbo Institute of Materials Technology and Engineering Chinese Academy of Sciences Ningbo 315201 P. R. China

Funding

National Natural Science Foundation of China · Research Grants Council, University Grants Committee

References (34)

Show source-provided references
1. 10.1038/3506900010.1038/35069000 ↗
2. 10.1038/nmat270410.1038/nmat2704 ↗
3. 10.1126/science.122085410.1126/science.1220854 ↗
4. 10.1002/anie.20080334110.1002/anie.200803341 ↗
5. 10.1021/acsbiomaterials.5b0015210.1021/acsbiomaterials.5b00152 ↗
6. 10.1016/j.actbio.2013.08.02010.1016/j.actbio.2013.08.020 ↗
7. 10.1016/j.mtcomm.2018.10.00510.1016/j.mtcomm.2018.10.005 ↗
8. 10.1042/BST037067710.1042/BST0370677 ↗
9. 10.1371/journal.pone.005812010.1371/journal.pone.0058120 ↗
10. 10.1676/11-148.110.1676/11-148.1 ↗
11. 10.1021/acsmacrolett.7b0000610.1021/acsmacrolett.7b00006 ↗
12. 10.1186/1475-2859-3-1410.1186/1475-2859-3-14 ↗
13. 10.1021/acs.biomac.8b0098010.1021/acs.biomac.8b00980 ↗
14. 10.1002/adma.20140423410.1002/adma.201404234 ↗
15. 10.1021/acsami.7b0863610.1021/acsami.7b08636 ↗
16. 10.1038/natrevmats.2018.810.1038/natrevmats.2018.8 ↗
17. 10.1529/biophysj.106.08914410.1529/biophysj.106.089144 ↗
18. 10.1016/S1369-7021(11)70057-810.1016/S1369-7021(11)70057-8 ↗
19. 10.1021/acs.biomac.6b0085710.1021/acs.biomac.6b00857 ↗
20. 10.1093/molbev/msh20410.1093/molbev/msh204 ↗
21. 10.1371/journal.pone.005022710.1371/journal.pone.0050227 ↗
22. 10.1039/C8CC05246H10.1039/C8CC05246H ↗
23. 10.1021/ma034573i10.1021/ma034573i ↗
24. 10.1021/bm060199t10.1021/bm060199t ↗
25. 10.3390/polym1003033310.3390/polym10030333 ↗
26. 10.3390/app712125810.3390/app7121258 ↗
27. 10.3390/polym1006063710.3390/polym10060637 ↗
28. 10.1021/bm034291q10.1021/bm034291q ↗
29. 10.1038/natrevmats.2018.1610.1038/natrevmats.2018.16 ↗
30. 10.1002/anie.20180234110.1002/anie.201802341 ↗
31. 10.1016/j.jmbbm.2010.09.00810.1016/j.jmbbm.2010.09.008 ↗
32. 10.1021/acsbiomaterials.6b0066910.1021/acsbiomaterials.6b00669 ↗
33. 10.1002/adfm.20140216710.1002/adfm.201402167 ↗
34. 10.1088/0964-1726/15/6/00610.1088/0964-1726/15/6/006 ↗