Copper-free click chemistry as an emerging tool for the programmed ligation of DNA-functionalised gold nanoparticles

被引:51
|
作者
Heuer-Jungemann, Amelie [1 ]
Kirkwood, Robert [1 ]
El-Sagheer, Afaf H. [2 ,3 ]
Brown, Tom [2 ,4 ]
Kanaras, Antonios G. [1 ,4 ]
机构
[1] Univ Southampton, Fac Phys Sci & Engn, Southampton SO17 1BJ, Hants, England
[2] Univ Southampton, Fac Nat & Environm Sci, Southampton SO17 1BJ, Hants, England
[3] Suez Univ, Chem Branch, Dept Sci & Math, Fac Petr & Min Engn, Suez 43721, Egypt
[4] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
SPHERICAL NUCLEIC-ACIDS; TERMINAL ALKYNES; NANOSTRUCTURES; TEMPLATES; NANORODS; AZIDES;
D O I
10.1039/c3nr02362a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate a new method to program the ligation of single stranded DNA-modified gold nanoparticles using copper-free click chemistry. Gold nanoparticles functionalized with a discrete number of 3'-azide or 5'-alkyne modified oligonucleotides, can be brought together via a splint strand and covalently 'clicked', in a simple one-pot reaction. This new approach to the assembly of gold nanoparticles is inherently advantageous in comparison to the traditional enzymatic ligation. The chemical ligation is specific and takes place at room temperature by simply mixing the particles without the need for special enzymatic conditions. The yield of 'clicked' nanoparticles can be as high as 92%. The ease of the copper-free, 'click-ligation' method allows for its universal applicability and opens up new avenues in programmed nanoparticle organization.
引用
收藏
页码:7209 / 7212
页数:4
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