DNA
纳米结构
纳米技术
基础(线性代数)
化学
生物物理学
材料科学
结晶学
化学物理
生物
生物化学
数学
几何学
作者
M. Andrey Joaqui‐Joaqui,Srikanth Dasari,Poornenth Pushpanandan,Valérie C. Pierre
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-10-10
卷期号:25 (42): 15264-15271
标识
DOI:10.1021/acs.nanolett.5c03742
摘要
Biomedical applications of DNA nanostructures are severely limited by the instability of DNA in serum due to nuclease activity. The self-assembly of metallointercalators in a DNA tetrahedron significantly enhances both the serum stability and the cellular uptake of the DNA nanostructure. Ancillary ligands and metal ions also significantly influence the stability of these nanoassemblies. Three complexes were synthesized, and the stability of the metallointercalator@DNA tetrahedron assembly in serum decreases in the order [PtII-(dppz)(py-4NH2)2]2+ > [PtII-(dppz)(en)]2+ > [EuIII-(dppz)(EDTA-BMA)]+, a trend that mirrors the affinity of the metallointercalator for the DNA nanostructure and the increase in the melting point of the assembly upon metallointercalation. [PtII-(dppz)(py-4NH2)2]2+ has hydrophobic 4-aminopyridine as the ancillary ligand that likely interacts with the minor groove of DNA. An efficient metallointercalator with ancillary ligands that can occupy the major groove pockets or minor groove provides greater stabilization of DNA nanostructures in serum necessary for biomedical applications.
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