Bipartite design of a self-fibrillating protein copolymer with nanopatterned peptide display capabilities

dc.contributor.authorBruning, Marc
dc.contributor.authorKreplak, Laurent
dc.contributor.authorLeopoldseder, Sonja
dc.contributor.authorMüller, Shirley A.
dc.contributor.authorRingler, Philippe
dc.contributor.authorDuchesne, Laurence
dc.contributor.authorFernig, David G
dc.contributor.authorEngel, Andreas
dc.contributor.authorUcurum-Fotiadis, Zöhre
dc.contributor.authorMayans, Olga
dc.date.accessioned2018-04-11T08:23:00Z
dc.date.available2018-04-11T08:23:00Z
dc.date.issued2010eng
dc.description.abstractThe development of biomatrices for technological and biomedical applications employs self-assembled scaffolds built from short peptidic motifs. However, biopolymers composed of protein domains would offer more varied molecular frames to introduce finer and more complex functionalities in bioreactive scaffolds using bottom-up approaches. Yet, the rules governing the three-dimensional organization of protein architectures in nature are complex and poorly understood. As a result, the synthetic fabrication of ordered protein association into polymers poses major challenges to bioengineering. We have now fabricated a self-assembling protein nanofiber with predictable morphologies and amenable to bottom-up customization, where features supporting function and assembly are spatially segregated. The design was inspired by the cross-linking of titin filaments by telethonin in the muscle sarcomere. The resulting fiber is a two-protein system that has nanopatterned peptide display capabilities as shown by the recruitment of functionalized gold nanoparticles at regular intervals of ∼ 5 nm, yielding a semiregular linear array over micrometers. This polymer promises the uncomplicated display of biologically active motifs to selectively bind and organize matter in the fine nanoscale. Further, its conceptual design has high potential for controlled plurifunctionalization.eng
dc.description.versionpublishedeng
dc.identifier.doi10.1021/nl1024886eng
dc.identifier.pmid20954695eng
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/42007
dc.language.isoengeng
dc.subjectNanofiber, protein polymer, protein engineering, self-assembly, biomaterial, peptide display system, gold nanoparticles, 1D arrayeng
dc.subject.ddc570eng
dc.titleBipartite design of a self-fibrillating protein copolymer with nanopatterned peptide display capabilitieseng
dc.typeJOURNAL_ARTICLEeng
dspace.entity.typePublication
kops.citation.bibtex
@article{Bruning2010Bipar-42007,
  year={2010},
  doi={10.1021/nl1024886},
  title={Bipartite design of a self-fibrillating protein copolymer with nanopatterned peptide display capabilities},
  number={11},
  volume={10},
  issn={1530-6984},
  journal={Nano letters},
  pages={4533--4537},
  author={Bruning, Marc and Kreplak, Laurent and Leopoldseder, Sonja and Müller, Shirley A. and Ringler, Philippe and Duchesne, Laurence and Fernig, David G and Engel, Andreas and Ucurum-Fotiadis, Zöhre and Mayans, Olga}
}
kops.citation.iso690BRUNING, Marc, Laurent KREPLAK, Sonja LEOPOLDSEDER, Shirley A. MÜLLER, Philippe RINGLER, Laurence DUCHESNE, David G FERNIG, Andreas ENGEL, Zöhre UCURUM-FOTIADIS, Olga MAYANS, 2010. Bipartite design of a self-fibrillating protein copolymer with nanopatterned peptide display capabilities. In: Nano letters. 2010, 10(11), pp. 4533-4537. ISSN 1530-6984. eISSN 1530-6992. Available under: doi: 10.1021/nl1024886deu
kops.citation.iso690BRUNING, Marc, Laurent KREPLAK, Sonja LEOPOLDSEDER, Shirley A. MÜLLER, Philippe RINGLER, Laurence DUCHESNE, David G FERNIG, Andreas ENGEL, Zöhre UCURUM-FOTIADIS, Olga MAYANS, 2010. Bipartite design of a self-fibrillating protein copolymer with nanopatterned peptide display capabilities. In: Nano letters. 2010, 10(11), pp. 4533-4537. ISSN 1530-6984. eISSN 1530-6992. Available under: doi: 10.1021/nl1024886eng
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kops.sourcefieldNano letters. 2010, <b>10</b>(11), pp. 4533-4537. ISSN 1530-6984. eISSN 1530-6992. Available under: doi: 10.1021/nl1024886deu
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kops.sourcefield.plainNano letters. 2010, 10(11), pp. 4533-4537. ISSN 1530-6984. eISSN 1530-6992. Available under: doi: 10.1021/nl1024886eng
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