纳米颗粒
纳米医学
生物分子
胶体金
共价键
纳米技术
DNA
配体(生物化学)
寡核苷酸
聚合物
化学
生物相容性
DNA折纸
碱基对
材料科学
纳米结构
有机化学
受体
生物化学
作者
José M. Carnerero,Aila Jimenez‐Ruiz,Paula M. Castillo,Rafael Prado‐Gotor
出处
期刊:ChemPhysChem
[Wiley]
日期:2016-10-13
卷期号:18 (1): 17-33
被引量:104
标识
DOI:10.1002/cphc.201601077
摘要
The interactions of DNA, whether long, hundred base pair chains or short-chained oligonucleotides, with ligands play a key role in the field of structural biology. Its biological activity not only depends on the thermodynamic properties of DNA-ligand complexes, but can and often is conditioned by the formation kinetics of those complexes. On the other hand, gold nanoparticles have long been known to present excellent biocompatibility with biomolecules and are themselves remarkable for their structural, electronic, magnetic, optical and catalytic properties, radically different from those of their counterpart bulk materials, and which make them an important asset in multiple applications. Therefore, thermodynamic and kinetic studies of the interactions of DNA with nanoparticles acting as small ligands are key for a better understanding of those interactions to allow for their control and modulation and for the opening of new venues of research in nanomedicine, analytic and biologic fields. The interactions of gold nanoparticles with both DNA polymers and their smaller subunits; special focus is placed on those interactions taking place with nonfunctionalized gold nanoparticles are reviewed in the present work.
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