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Stimuli-responsive assembly of bilingual peptide nucleic acids

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 a...

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Autores principales: Argueta-Gonzalez, Hector S., Swenson, Colin S., Song, George, Heemstra, Jennifer M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347363/
https://www.ncbi.nlm.nih.gov/pubmed/35974999
http://dx.doi.org/10.1039/d2cb00020b
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author Argueta-Gonzalez, Hector S.
Swenson, Colin S.
Song, George
Heemstra, Jennifer M.
author_facet Argueta-Gonzalez, Hector S.
Swenson, Colin S.
Song, George
Heemstra, Jennifer M.
author_sort Argueta-Gonzalez, Hector S.
collection PubMed
description 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.
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spelling pubmed-93473632022-08-15 Stimuli-responsive assembly of bilingual peptide nucleic acids Argueta-Gonzalez, Hector S. Swenson, Colin S. Song, George Heemstra, Jennifer M. RSC Chem Biol Chemistry 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. RSC 2022-06-17 /pmc/articles/PMC9347363/ /pubmed/35974999 http://dx.doi.org/10.1039/d2cb00020b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Argueta-Gonzalez, Hector S.
Swenson, Colin S.
Song, George
Heemstra, Jennifer M.
Stimuli-responsive assembly of bilingual peptide nucleic acids
title Stimuli-responsive assembly of bilingual peptide nucleic acids
title_full Stimuli-responsive assembly of bilingual peptide nucleic acids
title_fullStr Stimuli-responsive assembly of bilingual peptide nucleic acids
title_full_unstemmed Stimuli-responsive assembly of bilingual peptide nucleic acids
title_short Stimuli-responsive assembly of bilingual peptide nucleic acids
title_sort stimuli-responsive assembly of bilingual peptide nucleic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347363/
https://www.ncbi.nlm.nih.gov/pubmed/35974999
http://dx.doi.org/10.1039/d2cb00020b
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