期刊
ACS NANO
卷 3, 期 9, 页码 2751-2759出版社
AMER CHEMICAL SOC
DOI: 10.1021/nn9005768
关键词
gold nanoparticles; silver nanoparticles; colorimetric assay; peptide nucleic acids; DNA hybridization; single-base-mismatch discrimination
We have demonstrated that mixed-base PNA oligomers are effective coagulants of citrate ion-coated gold and silver nanoparticles (AuNPs and AgNPs), and PNA-induced particle aggregation can be disrupted by hybridization of PNA with a specific DNA. Using particles' aggregation/dispersion as a measure, we have investigated how PNA and PNA-DNA complexes bind to AuNPs and AgNPs and modulate particles' stability differently relative to their DNA counterparts, We have made the following original discoveries: (1) mix-base PNA oligomers can induce immediate particle aggregation in a concentration- and chain-length-dependent manner; (2) PNA oligomers have a higher affinity to AuNPs and AgNPs than its ssDNA counterpart; (3) PNA-DNA complexes, although having a stable double helix structure similar to dsDNA, can effectively protect the particles from salt induced aggregation, and the protection effect of different nucleic acids are in the order of PNA-DNA complex > ssDNA > dsDNA; (4) all the characteristics are identical for AuNPs and AgNPs; and (5) AgNPs is more sensitive in response to destabilization effect and is proven a more sensitive platform for colorimetric assays. The control of particle aggregation and dispersion by PNA and PNA-DNA complexes has been used to detect a specific DNA sequence with single-base-mismatch resolution. zeta potential measurements have been conducted to reveal how distinct backbone properties of PNA and PNA-DNA complexes relative to their DNA counterparts contribute to the distinct binding characteristics.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据