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Organization of self-assembled peptide-polymer nanofibers in solution
被引:54
|作者:
Borner, Hans G.
[1
]
Smarsly, Bernd M.
[1
]
Hentschel, Jens
[1
]
Rank, Anja
[2
]
Schubert, Rolf
[2
]
Geng, Yan
[3
]
Discher, Dennis E.
[4
]
Hellweg, Thomas
[5
]
Brandt, Astrid
[6
]
机构:
[1] Max Planck Inst Colloids & Interfaces, MPI KGF Golm, D-14424 Potsdam, Germany
[2] Univ Freiburg, Dept Pharmaceut Technol & Biopharm, D-79104 Freiburg, Germany
[3] Univ Georgia, Dept Chem, Athens, GA 30602 USA
[4] Univ Penn, Philadelphia, PA 19104 USA
[5] Univ Bayreuth, D-95447 Bayreuth, Germany
[6] Hahn Meitner Inst Berlin GmbH, D-14109 Berlin, Germany
关键词:
D O I:
10.1021/ma0714060
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
The solution structure and the aggregation behavior of stiff polymer-peptide nanofibers, self-assembled from well-defined poly(ethylene oxide)-peptide conjugates are described. Aqueous solutions at different concentrations of core-shell nanofibers were investigated by cryo-fixation transmission electron microscopy (cryoTEM) and small-angle neutron scattering (SANS). Both methods show the presence of stiff, extended nanofibers in dilute solution, providing nanodimensions for the fiber cross section, which are in good agreement with previously shown investigations on dried and deposited fibers. Moreover the previously suggested coreshell character of the fiber cross section could be verified by SANS density Profiles. In concentrated solutions exceeding 2 mg/mL, the nanofibers tended to further organize into nematic "bundles". Polarized optical microscopy (POM) indeed shows birefringence of the solutions and typical Schlieren textures in shear oriented films, consistent with high aspect ratio nanofibers. The results of this investigation are discussed in the context of the Flory theory of rigid rods.
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页码:1430 / 1437
页数:8
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