Nucleobase Amino Acids in the Development of Amide‐Linked Oligonucleotide Mimics

Although peptide nucleic acids (PNAs) have been extensively used in antisense strategies, the lack of any side chain in the PNA backbone deprives them of having any protein-like tertiary structures, limiting their use in nucleic acid-protein interactions. To overcome this limitation, scientists have developed hybrid monomeric structures like nucleobase amino acids (NBAs) where canonical nucleobases are covalently attached to natural or unnatural amino acid side chains, making them amenable to incorporation into peptides, proteins, and PNAs using solid- or solution-phase peptide synthesis. The resulting assemblies are capable of recognizing their complementary oligonucleotides as well as having the ability to form well-defined secondary/tertiary protein-like structures for enhanced nucleic acid-protein interactions. This perspective article chronicles the developments in this area of research over the years.

Authors

Institutions

Publication Details

Journal
ChemMedChem
Published
2026-07-26
DOI
https://doi.org/10.1002/cmdc.70404
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Nucleobase Amino Acids in the Development of Amide‐Linked Oligonucleotide Mimics

Tushar Kanti Chakraborty, Epsheeta Baruah
ChemMedChem
DNA and Nucleic Acid Chemistry
article

Nucleobase Amino Acids in the Development of Amide‐Linked Oligonucleotide Mimics

Tushar Kanti Chakraborty, Epsheeta Baruah
article en

Abstract

Although peptide nucleic acids (PNAs) have been extensively used in antisense strategies, the lack of any side chain in the PNA backbone deprives them of having any protein-like tertiary structures, limiting their use in nucleic acid-protein interactions. To overcome this limitation, scientists have developed hybrid monomeric structures like nucleobase amino acids (NBAs) where canonical nucleobases are covalently attached to natural or unnatural amino acid side chains, making them amenable to incorporation into peptides, proteins, and PNAs using solid- or solution-phase peptide synthesis. The resulting assemblies are capable of recognizing their complementary oligonucleotides as well as having the ability to form well-defined secondary/tertiary protein-like structures for enhanced nucleic acid-protein interactions. This perspective article chronicles the developments in this area of research over the years.

ChemMedChemVol. 21(14)
Indian Institute of Science Bangalore (IN)
Openalex Percentile: Top 15%
DNA and Nucleic Acid Chemistry
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.