Shihua Yu , Xiaoyan Dai , Haodong Wang , Xiaogang Ye , Xiangping Dai , Xinqiu Wang , Huoqing Zheng , Guijun Zhang , Boxiong Zhong
{"title":"工程蚕丝-蜘蛛复合丝的结构和力学性能。","authors":"Shihua Yu , Xiaoyan Dai , Haodong Wang , Xiaogang Ye , Xiangping Dai , Xinqiu Wang , Huoqing Zheng , Guijun Zhang , Boxiong Zhong","doi":"10.1016/j.actbio.2025.07.056","DOIUrl":null,"url":null,"abstract":"<div><div>Spider silk demonstrates significant potential for biomaterials and medicinal applications owing to its favorable mechanical properties and biocompatibility. However, spiders are difficult to raise on a large scale, and obtaining silk proteins directly from spiders is inefficient and expensive. A promising strategy for addressing these challenges involves expressing spider silk proteins in transgenic silkworms. In this study, transcription activator-like effector nuclease (TALEN)-mediated genome-targeted editing was employed to separately fuse 1-, 2-, 4-, and eightfold repeats of the <em>cre-MaSp1</em> gene from black widow spiders to the <em>sericin 1</em> gene. AlphaFold 3 structure prediction and infrared spectroscopy showed that the β-sheet and helix contents of the composite silk proteins progressively increased with the increase in the number of fused cre-MaSp1 repeats. Mechanical property testing showed that the maximum stress and maximum strain of the silkworm-spider composite silk containing the eightfold cre-MaSp1/Ser1 fusion protein were 39.4 % and 62.2 % higher than those of the wild-type, respectively, representing the best performance among all the lines. This study provides insights into sericin modification and further confirms that the expression of the <em>cre-MaSp1</em> gene harboring a large number of repeats can improve the mechanical properties of silkworm silk.</div></div><div><h3>Statement of significance</h3><div>Silkworm silk is a kind of natural protein fiber, and the improvement of silk performance is a long-term focus. This study aims to improve the mechanical properties of silk by endowing it with functional proteins through targeted modification of silk proteins. Four different repeats of <em>cre-MaSp1</em> gene from black widow spiders separately fused into endogenous Ser1 by TALEN-mediated homology-directed recombination. The fusion proteins were successfully expressed and secreted into the cocoon shell. Tensile testing indicated that eightfold cre-MaSp1 repeats significantly increased the maximum stress and strain of the composite silk by 39.4 % and 62.2 % over the wild-type, respectively. Our work provides insights into improving silk properties and expands the potential applications of the silkworm silk gland bioreactor.</div></div>","PeriodicalId":237,"journal":{"name":"Acta Biomaterialia","volume":"203 ","pages":"Pages 245-255"},"PeriodicalIF":9.6000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structural and mechanical properties of engineered silkworm-spider composite silk\",\"authors\":\"Shihua Yu , Xiaoyan Dai , Haodong Wang , Xiaogang Ye , Xiangping Dai , Xinqiu Wang , Huoqing Zheng , Guijun Zhang , Boxiong Zhong\",\"doi\":\"10.1016/j.actbio.2025.07.056\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Spider silk demonstrates significant potential for biomaterials and medicinal applications owing to its favorable mechanical properties and biocompatibility. However, spiders are difficult to raise on a large scale, and obtaining silk proteins directly from spiders is inefficient and expensive. A promising strategy for addressing these challenges involves expressing spider silk proteins in transgenic silkworms. In this study, transcription activator-like effector nuclease (TALEN)-mediated genome-targeted editing was employed to separately fuse 1-, 2-, 4-, and eightfold repeats of the <em>cre-MaSp1</em> gene from black widow spiders to the <em>sericin 1</em> gene. AlphaFold 3 structure prediction and infrared spectroscopy showed that the β-sheet and helix contents of the composite silk proteins progressively increased with the increase in the number of fused cre-MaSp1 repeats. Mechanical property testing showed that the maximum stress and maximum strain of the silkworm-spider composite silk containing the eightfold cre-MaSp1/Ser1 fusion protein were 39.4 % and 62.2 % higher than those of the wild-type, respectively, representing the best performance among all the lines. This study provides insights into sericin modification and further confirms that the expression of the <em>cre-MaSp1</em> gene harboring a large number of repeats can improve the mechanical properties of silkworm silk.</div></div><div><h3>Statement of significance</h3><div>Silkworm silk is a kind of natural protein fiber, and the improvement of silk performance is a long-term focus. This study aims to improve the mechanical properties of silk by endowing it with functional proteins through targeted modification of silk proteins. Four different repeats of <em>cre-MaSp1</em> gene from black widow spiders separately fused into endogenous Ser1 by TALEN-mediated homology-directed recombination. The fusion proteins were successfully expressed and secreted into the cocoon shell. Tensile testing indicated that eightfold cre-MaSp1 repeats significantly increased the maximum stress and strain of the composite silk by 39.4 % and 62.2 % over the wild-type, respectively. Our work provides insights into improving silk properties and expands the potential applications of the silkworm silk gland bioreactor.</div></div>\",\"PeriodicalId\":237,\"journal\":{\"name\":\"Acta Biomaterialia\",\"volume\":\"203 \",\"pages\":\"Pages 245-255\"},\"PeriodicalIF\":9.6000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Biomaterialia\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1742706125005549\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Biomaterialia","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1742706125005549","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
Structural and mechanical properties of engineered silkworm-spider composite silk
Spider silk demonstrates significant potential for biomaterials and medicinal applications owing to its favorable mechanical properties and biocompatibility. However, spiders are difficult to raise on a large scale, and obtaining silk proteins directly from spiders is inefficient and expensive. A promising strategy for addressing these challenges involves expressing spider silk proteins in transgenic silkworms. In this study, transcription activator-like effector nuclease (TALEN)-mediated genome-targeted editing was employed to separately fuse 1-, 2-, 4-, and eightfold repeats of the cre-MaSp1 gene from black widow spiders to the sericin 1 gene. AlphaFold 3 structure prediction and infrared spectroscopy showed that the β-sheet and helix contents of the composite silk proteins progressively increased with the increase in the number of fused cre-MaSp1 repeats. Mechanical property testing showed that the maximum stress and maximum strain of the silkworm-spider composite silk containing the eightfold cre-MaSp1/Ser1 fusion protein were 39.4 % and 62.2 % higher than those of the wild-type, respectively, representing the best performance among all the lines. This study provides insights into sericin modification and further confirms that the expression of the cre-MaSp1 gene harboring a large number of repeats can improve the mechanical properties of silkworm silk.
Statement of significance
Silkworm silk is a kind of natural protein fiber, and the improvement of silk performance is a long-term focus. This study aims to improve the mechanical properties of silk by endowing it with functional proteins through targeted modification of silk proteins. Four different repeats of cre-MaSp1 gene from black widow spiders separately fused into endogenous Ser1 by TALEN-mediated homology-directed recombination. The fusion proteins were successfully expressed and secreted into the cocoon shell. Tensile testing indicated that eightfold cre-MaSp1 repeats significantly increased the maximum stress and strain of the composite silk by 39.4 % and 62.2 % over the wild-type, respectively. Our work provides insights into improving silk properties and expands the potential applications of the silkworm silk gland bioreactor.
期刊介绍:
Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.