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| Research article summary (published 23 May 2007): |
Expression of EGFP-spider dragline silk fusion protein in BmN cells and larvae of silkworm showed the solubility is primary limit for dragline proteins yield.
Full Abstract
Spider dragline silk is a unique fibrous protein with combination of tensile strength and elasticity, but the isolation of large amount of silk from spiders is not feasible. In this paper, we used a newly established Bac-to-Bac/BmNPV Baculovirus expression system to express the recombinant spider (Nephila clavata) dragline silk protein (MaSp1) fused EGFP in BmN cells and larvae of silkworm. A 70 kDa fusion protein was visualized after rBacmid/BmNPV/drag infection by SDS-PAGE and immunoblotting analysis. Fusion protein expressed in the BmN cells probably occupied five percent of the cell total protein; In a silkworm larva, approximately 6 mg fusion proteins were expressed. Solubility analysis of the expressed spider dragline silk protein indicated that 60% fusion protein is insoluble. EGFP fluorescence showed that fusion protein is tend to form aggregate by self assemblage. The results indicated the solubility is the primary limit for spider dragline proteins yield. It also suggested that directly produce fibrous spider silk in the secreting-silk organs of the transgenic silkworm larvae might be a better method.
Author information
Author/s: Zhang, Yuansong (Y); Hu, Junhua (J); Miao, Yungen (Y); Zhao, Aichun (A); Zhao, Tianfu (T); Wu, Dayang (D); Liang, Liefeng (L); Miikura, Ayumi (A); Shiomi, Kunihiro (K); Kajiura, Zenta (Z); Nakagaki, Masao (M);
Affiliation: Department of Applied Biology, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano, Japan. zyshjh(-atsign-)hotmail.com
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: Molecular biology reports (Mol Biol Rep), published in Netherlands. (Language: eng)
Reference: 2008-Sep; vol 35 (issue 3) : pp 329-35
Dates: Created 2008/07/28; Completed 2008/09/26;
PMID: 17525867, status: MEDLINE (last retrieved date: 2/18/2009)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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Associated Chemicals: DNA, Complementary (0) ; Recombinant Fusion Proteins (0) ; Fibroins (9007-76-5)Related articles
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