New cylindrical peptide assemblies defined by extended parallel β-sheets

A new approach to non-covalent peptide-based nanotubular or rod-like structures is presented, whereby the monomeric units are preorganised into a β-strand geometry that templates the formation of an extended and unusual parallel β-sheet rod-like structure. The conformational constraint is introduced...

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Veröffentlicht in:Organic & biomolecular chemistry 2013-01, Vol.11 (3), p.425-429
Hauptverfasser: Pehere, Ashok D, Sumby, Christopher J, Abell, Andrew D
Format: Artikel
Sprache:eng
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Zusammenfassung:A new approach to non-covalent peptide-based nanotubular or rod-like structures is presented, whereby the monomeric units are preorganised into a β-strand geometry that templates the formation of an extended and unusual parallel β-sheet rod-like structure. The conformational constraint is introduced by Huisgen cycloaddition to give a triazole-based macrocycle, with the resulting self-assembled structures stabilized by a well-defined series of intermolecular hydrogen bonds.
ISSN:1477-0520
1477-0539
DOI:10.1039/c2ob26637g