Nucleic acid-based supramolecular structures: vesicular spherical nucleic acids from a non-phospholipid nucleolipid. Issue 18 (15th August 2022)

• Record Type: Journal Article
• Authors: Dimitrov, Erik; Toncheva-Moncheva, Natalia; Bakardzhiev, Pavel; Forys, Aleksander; Doumanov, Jordan; Mladenova, Kirilka; Petrova, Svetla; Trzebicka, Barbara; Rangelov, Stanislav
• Is Part Of: Nanoscale advances. Volume 4:Issue 18(2022)
• Page Start: 3793
• Page End: 3803
• Publication Date: 2022-08-15
• Subjects: 620.5
• DOI: 10.1039/d2na00527a
• Languages: English
• ISSNs: 2516-0230

Abstract

Abstract : An original hybrid biomacromolecule, consisting of a lipid-mimetic residue and a 21-base long nucleic acid strand, spontaneously self-associates and co-associates with other lipids into nucleic acid-grafted vesicular structures. Abstract : Vesicular spherical nucleic acids are dynamic nucleic acid-based supramolecular structures that are held together via non-covalent bonds. They have promising applications as drug and nucleic acid delivery materials, diagnostic and imaging tools and platforms for development of various therapeutic schemes. In this contribution, we report on vesicular spherical nucleic acids, constructed from a non-phospholipid nucleolipid – an original hybrid biomacromolecule, composed of a hydrophobic residue, resembling that of the naturally occurring phospholipids, and a DNA oligonucleotide strand. The nucleolipid was synthesized by coupling of dibenzocyclooctyne-functionalized oligonucleotide and azidated 1, 3-dihexadecyloxy-propane-2-ol via an azide–alkyne click reaction. In aqueous solution it spontaneously self-associated into nanosized supramolecular structures, identified as unilamellar vesicles composed of a self-closed interdigitated bilayer. Vesicular structures were also formed upon intercalation of the nucleolipid via its lipid-mimetic residue in the phospholipid bilayer membrane of liposomes prepared from readily available and FDA-approved lipids (1, 2-dipalmitoyl- rac-glycero -3-phosphocholine and cholesterol). The vesicular structures are thoroughly investigated by light scattering (dynamic, static, and electrophoretic) and cryogenic TEM and the physical characteristics, in particular, number of strands per particle, grafting density, and conformation of the strands, were compared to those of reference spherical nucleic acids. Finally, the vesicular structures were shown to exhibit cellular internalization with no need of transfection agents and enhanced colloidal and nuclease stability.