Sterilized Recombinant Spider Silk Fibers of Low Pyrogenicity

被引:48
作者
Hedhammar, My [1 ]
Bramfeldt, Hanna [1 ]
Baris, Teodora [2 ]
Widhe, Mona [1 ]
Askarieh, Glareh [3 ]
Nordling, Kerstin [1 ]
von Aulock, Sonja [2 ]
Johansson, Jan [1 ]
机构
[1] Swedish Univ Agr Sci, Dept Anat Physiol & Biochem, Uppsala Biomed Ctr, SE-75123 Uppsala, Sweden
[2] Univ Konstanz, D-78464 Constance, Germany
[3] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
基金
瑞典研究理事会;
关键词
ENDOTOXIN REMOVAL; ESCHERICHIA-COLI; CHROMATOGRAPHIC REMOVAL; AFFINITY-CHROMATOGRAPHY; PROTEIN SOLUTIONS; LIPOPOLYSACCHARIDE; BIOMATERIAL; EFFICIENCY; PROTOCOL; RELEASE;
D O I
10.1021/bm9014039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have recently shown that it is possible to recombinantly produce a miniature spider silk protein, 4RepCT, that spontaneously self-assembles into mechanically stable macroscopic fibers (Stark, M.; Grip, S.; Rising, A.; Hedhammar, M.; Engstrom, W.; Hjalm, G.; Johansson, J. Macroscopic fibers self-assembled from recombinant miniature spider silk proteins. Biomacromolecules 2007, 8 (5), 1695-1701). When produced as a soluble fusion protein (with thioredoxin) in Escherichia con, the spider silk protein can be subjected to several purification steps without aggregating. Here, combined purification and endotoxin removal is achieved using a simple cell wash procedure, protein affinity purification, and LIDS depletion. No toxic chemicals were included in the process and the protein retained its ability to self-assemble into fibers. With this method, fibers with pyrogenicity corresponding to less than 1 EU/mg could be recovered. Moreover, the fibers could be sterilized through autoclaving with retained morphology, structure, and mechanical properties. This implies that this recombinant silk is suitable for usage as biomaterial, which is further supported by data showing that the fibers allow growth of human primary fibroblasts.
引用
收藏
页码:953 / 959
页数:7
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