Imaging gold nanoparticles for DNA sequence recognition in biomedical applications

被引:19
作者
Eaton, Peter [1 ]
Doria, Goncalo [2 ]
Pereira, Eulalia [1 ]
Baptista, Pedro Viana [2 ]
Franco, Ricardo [3 ]
机构
[1] Univ Porto, Fac Ciencias, Dept Quim, REQUIMTE, P-4169007 Oporto, Portugal
[2] Univ Nova Lisboa, Fac Ciencias & Tecnol, SABT, CIGMH, P-2829516 Caparica, Portugal
[3] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, REQUIMTE, P-2829516 Caparica, Portugal
关键词
atomic force microscopy; biological materials; biomedical transducers; DNA; nanotechnology;
D O I
10.1109/TNB.2007.908985
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The hybridization of single-stranded oligonucleotide-derivatized gold nanoparticles (An nanoprobes) with double stranded complementary DNA was directly observed by atomic force microscopy (AFM). This specific interaction is the basis for an An nanoprobe-based homogeneous assay for specific DNA sequence detection, based on salt-induced particle aggregation that is prevented when a complementary target is present. For long DNA targets (linearized plasmid DNA) complicated hybridized target DNA-Au-nanoprobes structures were formed, that were interpreted as the basis for stability of the An nanoprobes against salt-induced aggregation. For shorter DNA targets (PCR amplified fragments) hybridization with the An nanoprobes occurred, in the majority of cases, in the expected location of the DNA target fragment containing the specific sequence. The formation of the observed DNA hybridized structures provides evidence at the molecular level for specific hybridization to the target sequence as the method of binding of the An nanoprobes.
引用
收藏
页码:282 / 288
页数:7
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