Engineering functional nanoparticles for delivery in cells

被引:0
|
作者
Alexaki, Konstantina [1 ]
Kyriazi, Maria Eleni [1 ]
El Sagheer, Afaf H. [3 ,4 ]
Brown, Tom [3 ]
Kanaras, Antonios G. [1 ,2 ]
机构
[1] Univ Southampton, Phys & Astron, Southampton SO17 1BJ, Hants, England
[2] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
[3] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
[4] Suez Univ, Fac Petr & Min Engn, Dept Sci & Math, Chem Branch, Suez 43721, Egypt
来源
COLLOIDAL NANOPARTICLES FOR BIOMEDICAL APPLICATIONS XV | 2020年 / 11255卷
关键词
DNA; peptide; nanoparticles; cells; mRNA detection; MESSENGER-RNA DETECTION; GOLD-NANOPARTICLES; NANO-FLARES; DNA; MECHANISM; SURFACE; PROBES;
D O I
10.1117/12.2538470
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The ability of DNA functionalised gold nanoparticles (AuNPs) to detect specific targets in vitro and in vivo has led to their development as suitable tools for sensing applications. However, endosomal entrapment is a common barrier in various nanoparticle delivery approaches. In this work, we present a new design strategy with the aim to enhance endosomal escape of DNA-coated AuNPs via the incorporation of a peptide that has been found to promote effective escape within cells. AuNPs are firstly modified with thiol terminated DNA strands followed by further surface functionalisation with cysteine terminated peptides. We show that optimized loading of peptides following DNA nanoparticle functionalisation of nanoparticles is feasible. DNA-peptide-coated AuNP hybrids show similar stability towards degradation by endocellular enzymes and similar specificity towards the detection of specific mRNA targets.
引用
收藏
页数:13
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