» Articles » PMID: 37456777

Nucleic Acid Amphiphiles: Synthesis, Properties, and Applications

Overview
Publisher Cell Press
Date 2023 Jul 17
PMID 37456777
Authors
Affiliations
Soon will be listed here.
Abstract

Nucleic acid amphiphiles, referring to nucleic acids modified with large hydrophobic groups, have been widely used in programmable bioengineering. Since nucleic acids are intrinsically hydrophilic, the hydrophobic groups endow nucleic acid amphiphiles with unique properties, such as self-assembling, interactions with artificial or biological membranes, and transmembrane transport. Importantly, the hybridization or target binding capability of oligonucleotide itself supplies nucleic acid amphiphiles with excellent programmability. As a result, this type of molecule has attracted considerable attention in academic studies and has enormous potential for further applications. For a comprehensive understanding of nucleic acid amphiphiles, we review the reported research on nucleic acid amphiphiles from their molecular design to final applications, in which we summarize the synthetic strategies for nucleic acid amphiphiles and draw much attention to their unique properties in different contexts. Finally, a summary of the applications of nucleic acid amphiphiles in drug development, bioengineering, and bioanalysis are critically discussed.

Citing Articles

Development of Small Interfering RNA Loaded Cationic Lipid Nanoparticles for the Treatment of Liver Cancer with Elevated α-Fetoprotein Expression.

Duangchan K, Limjunyawong N, Rodponthukwaji K, Ittiudomrak T, Thaweesuvannasak M, Kunwong N ACS Bio Med Chem Au. 2025; 5(1):78-88.

PMID: 39990947 PMC: 11843345. DOI: 10.1021/acsbiomedchemau.4c00061.


Peptide Aptamer-Paclitaxel Conjugates for Tumor Targeted Therapy.

Shen X, Ma Y, Luo H, Abdullah R, Pan Y, Zhang Y Pharmaceutics. 2025; 17(1).

PMID: 39861688 PMC: 11768741. DOI: 10.3390/pharmaceutics17010040.


Form Equals Function: Influence of Coacervate Architecture on Drug Delivery Applications.

Lim C, Blocher McTigue W ACS Biomater Sci Eng. 2024; 10(11):6766-6789.

PMID: 39423330 PMC: 11558567. DOI: 10.1021/acsbiomaterials.4c01105.


DNA-empowered synthetic cells as minimalistic life forms.

Samanta A, Baranda Pellejero L, Masukawa M, Walther A Nat Rev Chem. 2024; 8(6):454-470.

PMID: 38750171 DOI: 10.1038/s41570-024-00606-1.


Advances in Nucleic Acid Research: Exploring the Potential of Oligonucleotides for Therapeutic Applications and Biological Studies.

Moccia M, Pascucci B, Saviano M, Cerasa M, Terzidis M, Chatgilialoglu C Int J Mol Sci. 2024; 25(1).

PMID: 38203317 PMC: 10778772. DOI: 10.3390/ijms25010146.

References
1.
Liu K, Zheng L, Liu Q, de Vries J, Gerasimov J, Herrmann A . Nucleic acid chemistry in the organic phase: from functionalized oligonucleotides to DNA side chain polymers. J Am Chem Soc. 2014; 136(40):14255-62. DOI: 10.1021/ja5080486. View

2.
Chan Y, van Lengerich B, Boxer S . Lipid-anchored DNA mediates vesicle fusion as observed by lipid and content mixing. Biointerphases. 2010; 3(2):FA17. DOI: 10.1116/1.2889062. View

3.
Zhang Y, Peng R, Xu F, Ke Y . Hierarchical Self-Assembly of Cholesterol-DNA Nanorods. Bioconjug Chem. 2019; 30(7):1845-1849. PMC: 7254875. DOI: 10.1021/acs.bioconjchem.9b00322. View

4.
Du T, Yuan W, Zhao Z, Liu S . Reversible morphological tuning of DNA-perylenebisdiimide assemblies through host-guest interaction. Chem Commun (Camb). 2019; 55(25):3658-3661. DOI: 10.1039/c9cc00406h. View

5.
Kaur H, Bruno J, Kumar A, Sharma T . Aptamers in the Therapeutics and Diagnostics Pipelines. Theranostics. 2018; 8(15):4016-4032. PMC: 6096388. DOI: 10.7150/thno.25958. View