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Spherically Directed Synthesis and Enhanced Cellular Internalization of Metal-Crosslinked DNA Micelles
- Source :
- Chem. 5:913-928
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- Summary Using spherically directed reduction of metal ions, a facile and universal method for in situ crosslinking of DNA micelles is described. By incorporating a series of specific template domains into lipid-DNA monomers, copper-, silver-, and gold-crosslinked DNA micelles are formed. By combining characterization results and simulation algorithms, accurate structural profiling of DNA micelles is achieved for the first time. The prepared metal-crosslinked DNA micelles show obvious merits, including one-step formation of core structure and ligand corona, facile size tunability, monodispersity, stability against salt-induced aggregation, high utilization of DNA ligand, mild synthesis conditions, and less time consumption and better internalization. Based on our spherically directed synthesis, metal-crosslinked DNA micelle flares were further prepared for effective intracellular imaging by integrating an aptamer-toehold strategy. In addition, we extended the strategy to cholesterol-based double-stranded DNA micelles, giving strong evidence that our method is not only universal but also flexible.
- Subjects :
- In situ
General Chemical Engineering
media_common.quotation_subject
Metal ions in aqueous solution
chemistry.chemical_element
02 engineering and technology
010402 general chemistry
01 natural sciences
Biochemistry
Micelle
Metal
chemistry.chemical_compound
Materials Chemistry
Environmental Chemistry
Internalization
media_common
Biochemistry (medical)
General Chemistry
021001 nanoscience & nanotechnology
Copper
Combinatorial chemistry
0104 chemical sciences
Monomer
chemistry
visual_art
visual_art.visual_art_medium
0210 nano-technology
DNA
Subjects
Details
- ISSN :
- 24519294
- Volume :
- 5
- Database :
- OpenAIRE
- Journal :
- Chem
- Accession number :
- edsair.doi...........26f793591f1ec34c18c4dbc90db188ba
- Full Text :
- https://doi.org/10.1016/j.chempr.2019.02.004