Issue 8, 2022

Stimuli-responsive assembly of bilingual peptide nucleic acids

Abstract

Peptide nucleic acids (PNAs) are high-affinity synthetic nucleic acid analogs capable of hybridization with native nucleic acids. PNAs synthesized having amino acid sidechains installed at the γ-position along the backbone provide a template for a single biopolymer to simultaneously encode nucleic acid and amino acid sequences. Previously, we reported the development of “bilingual” PNAs through the synthesis of an amphiphilic sequence featuring separate blocks of hydrophobic and hydrophilic amino acid functional groups. These PNAs combined the sequence-specific binding activity of nucleic acids with the structural organization properties of peptides. Like other amphiphilic compounds, these γ-PNAs were observed to assemble spontaneously into micelle-like nanostructures in aqueous solutions and disassembly was induced through hybridization to a complementary sequence. Here, we explore whether assembly of these bilingual PNAs is possible by harnessing the nucleic acid code. Specifically, we designed an amphiphile-masking duplex system in which spontaneous amphiphile assembly is prevented through hybridization to a nucleic acid masking sequence. We show that the amphiphile is displaced upon introduction of a releasing sequence complementary to the masking sequence through toehold mediated displacement. Upon release, we observe that the amphiphile proceeds to assemble in a fashion consistent with our previously reported structures. Our approach represents a novel method for controlled stimuli-responsive assembly of PNA-based nanostructures.

Graphical abstract: Stimuli-responsive assembly of bilingual peptide nucleic acids

Supplementary files

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Article information

Article type
Paper
Submitted
21 Jan 2022
Accepted
16 Jun 2022
First published
17 Jun 2022
This article is Open Access
Creative Commons BY-NC license

RSC Chem. Biol., 2022,3, 1035-1043

Stimuli-responsive assembly of bilingual peptide nucleic acids

H. S. Argueta-Gonzalez, C. S. Swenson, G. Song and J. M. Heemstra, RSC Chem. Biol., 2022, 3, 1035 DOI: 10.1039/D2CB00020B

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