| Autor: |
Junger A; TU München, Lehrstuhl für Makromolekulare Stoffe, Lichtenbergstrasse 4, D-85747 Garching, Germany., Kaufmann D, Scheibel T, Weberskirch R |
| Jazyk: |
angličtina |
| Zdroj: |
Macromolecular bioscience [Macromol Biosci] 2005 Jun 24; Vol. 5 (6), pp. 494-501. |
| DOI: |
10.1002/mabi.200400213 |
| Abstrakt: |
A new protein engineering strategy was utilized to synthesize an elastin-mimetic polypeptide. The primary structure represents an elastic motif composed of thirty amino acids with one lysine and one glutamic acid per repeat unit EMM = (VPGVG VPGKG VGPVG VPGVG VPGEG VPGIG). The gene was constructed using a Seamless Cloning method by generating three DNA cassettes which all encoded the EMM repeat unit, but with different flanking restriction recognition sites. The DNA cassettes were assembled to yield a gene that could be directly cloned into the multiple cloning site of pBluescript II SK+. The resulting gene (EMM)(7) with approximately 650 base pairs in length was further cloned into the expression vector pET-28b. Protein biosynthesis in E. coli strain BLR(DE3) resulted in the 21.5 kDa repeating polypeptide His(6)-(EMM)(7) yielding up to 50 mg . L(-1) of cell culture. Secondary structure analysis by far UV circular dichroism revealed a minimum at 197 nm and a shoulder at 218 nm indicative for a random coil with some type II beta-turn conformation content. Lower critical solution temperature (LCST) behavior strongly depends on salt and polypeptide concentration. Importantly, first cross-linking experiments indicate successful hydrogel formation with a surface structure reminiscent to natural elastin as visualized by SEM micrographs. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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