Self-assemblies of electrostatically self-complementary peptides derived from different structural motifs Restricted; Files & ToC

Nguyen, Duong (Spring 2024)

Permanent URL: https://etd.library.emory.edu/concern/etds/n009w3841?locale=es
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Abstract

Supramolecular self-assembly from peptides is a powerful bottom-up approach for the fabrication of bio-nanomaterials. Peptides are advantageous among the sequence-programmable oligomers because of their sequence-specificity and chemical diversity, hence offering a great opportunity to introduce functional complexity across length-scales. However, it is currently still challenging to achieve controlled fabrication of structurally and dimensionally defined assemblies. This dissertation presents our effort in the fabrication of one- and two-dimensional nanomaterials from the self-assemblies of peptide sequences that are electrostatically self-complementary. The general construct of the peptides consists of two end blocks with oppositely charged residues and a midblock that is neutral. The peptide sequences are designed based on two structural motifs, collagen triple helices and -sheets. The collagen-mimetic peptides (CMPs) fold into triple helices, which subsequently self-assemble into two-dimensional crystalline nanosheets via electrostatic interaction. In this work, we utilize CMPs for the construction of multicomponent nanosheets with tunable properties. Even though our study of the -strand mimetic peptides (BMPs) is still at its infancy, preliminary results indicate that the charge-complementary sequence design in combination with D-amino acid substitution promote very robust growth of BMPs into one-dimensional nanotubes. Our current findings suggest that the relatively simple design of electrostatically self-complementary peptides works across multiple structural motifs and may present a promising strategy for controlled fabrication of peptide-based nanomaterials.

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