Abstract

Novel multiblock polypeptides with a structure similar to the unique sequence observed in spider silk proteins (spidroins) were synthesized via a two-step chemical synthesis method, that is, chemoenzymatic polymerization, using papain followed by postpolycondensation. Two types of polypeptide fragments were prepared by chemoenzymatic polymerization: polyalanine as a hard block, which forms β-sheets in the spider silk fibers, and poly(glycine-random-leucine) as a soft block. These two fragments were ligated by postpolycondensation using polyphosphoric acid as a condensing agent. Wide-angle X-ray diffraction (WAXD) and IR measurements revealed that the resulting multiblock polypeptides formed an antiparallel β-sheet structure with a degree of crystallinity similar to that of spider silk, which resulted in a fibrous morphology. This work provides the first example of a synthetic multiblock polypeptide mimicking the secondary structures of spider silk.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.