Controlling Supramolecular Chirality in Peptide−π-Peptide Networks by Variation of the Alkyl Spacer Length

March 24, 2020

Title

Controlling Supramolecular Chirality in Peptide−π-Peptide Networks by Variation of the Alkyl Spacer Length

Author

Sayak Subhra Panda, Kirill Shmilovich, Andrew L. Ferguson, John D. Tovar

Year

2019

Journal

Langmuir

Abstract

Self-assembled supramolecular organic materials with π-functionalities are of great interest because of their applications as biocompatible nanoelectronics. A detailed understanding of molecular parameters to modulate the formation of hierarchical structures can inform design principles for materials with engineered optical and electronic properties. In this work, we combine molecular-level characterization techniques with all-atom molecular simulations to investigate the subtle relationship between the chemical structure of peptide-π-peptide molecules and the emergent supramolecular chirality of their spontaneously self-assembled nanoaggregates. We demonstrate through circular dichroism measurements that we can modulate the chirality by incorporating alkyl spacers of various lengths in between the peptides and thienylene–phenylene π-system chromophores: even numbers of alkyl carbons in the spacer units (0, 2) induce M-type helical character whereas odd numbers (1, 3) induce P-type. Corroborating molecular dynamics simulations and explicating machine learning analysis techniques identify hydrogen bonding and hydrophobic packing to be the principal discriminants of the observed chirality switches. Our results present a molecular-level design rule to engineer chirality into optically and electronically active nanoaggregates of these peptidic building blocks by exploiting systematic variations in the alkyl spacer length.

Instrument

J-810

Keywords

Circular dichroism, Stereochemistry, Secondary structure, Nanostructures, Biochemistry, Materials