Synthesis and Evaluation of Self-Assembled Nanostructures of Peptide-π Chromophore Conjugates

Peptides provide a biomolecular scaffold for solubilizing and assembling π-conjugated molecules in aqueous media. The properties of such peptide-π chromophore conjugates can be manipulated by varying the constituent amino acid residues in the peptide backbone as well as the chromophore moieties. Suc...

Full description

Saved in:
Bibliographic Details
Published inMethods in molecular biology (Clifton, N.J.) Vol. 1777; p. 209
Main Authors Kale, Tejaswini S, Tovar, John D
Format Journal Article
LanguageEnglish
Published United States 2018
Subjects
Online AccessGet more information

Cover

Loading…
More Information
Summary:Peptides provide a biomolecular scaffold for solubilizing and assembling π-conjugated molecules in aqueous media. The properties of such peptide-π chromophore conjugates can be manipulated by varying the constituent amino acid residues in the peptide backbone as well as the chromophore moieties. Such a precise handle on molecular structure leads to molecules with diverse macromolecular and material properties. We developed a versatile synthetic protocol that leads to a wide range of peptide-π chromophore conjugates in which the chromophores are covalently attached to the peptide backbone such that the chromophore is flanked by two peptide chains. This "trimer" structure lends interesting self-assembly properties to these materials which may be useful for a plethora of biological applications.
ISSN:1940-6029
DOI:10.1007/978-1-4939-7811-3_12