Dipartimento di Chimica "Ugo Schiff", Università di Firenze, Via della Lastruccia 3-13, 50019 Sesto Fiorentino (FI), Italy.
Laboratoire de Réactivité de Surfaces, UMR CNRS 7197, Université Pierre & Marie Curie - Paris VI, Site d'Ivry - Le Raphae¨l, 94200 Ivry-sur-Seine, France; Laboratoire CSPBAT UMR7244, UFR Santé, Médecine et Biologie Humaine, Université Paris 13, 74 rue Marcel Cachin, 93017 Bobigny, France.
Biosens Bioelectron. 2015 Dec 15;74:981-8. doi: 10.1016/j.bios.2015.07.071. Epub 2015 Aug 1.
A Surface Plasmon Resonance imaging (SPRi) based DNA sensors for the selective and ultrasensitive human genomic DNA detection, directly extracted from lymphocytes (bypassing PCR amplification), is reported. To achieve DNA detection, a rationally chosen star-shaped nanoparticle (NP), namely gold nanostar (AuNS), has been applied, for the first time, in a sandwich-like assay based on the selective capturing of specific DNA targets and the subsequent signal amplification by a secondary DNA probe linked to AuNS. The plasmonic profile, size and electric field enhancements at the star tips contributed to the maximization of plasmon coupling between LSPs and SPs as aimed for analytical signal magnification. The system was first tested using short synthetic DNA target sequences and applied to DNA biosensing, lowering 610-fold the detection limit from 6.1 nM (without NSs labeling) to 10 pM (with NSs labeling). Then the biosensor was applied to genomic DNA samples, extracted from human lymphocytes and undergoing only to a simple ultrasonic fragmentation, lowering (~435 fold) the detection limit from 3.0 fM (without NSs labeling) to 6.9 aM (with NSs labeling). Thanks to the assay optimization, we proved that tuning the NSs surface coverage with DNA linked to nanoparticles is crucial not only for the increase of signals but also for the regenerability/reusability of the biosensor for tens of measurement cycles.
一种基于表面等离子体共振成像(SPRi)的 DNA 传感器,用于选择性和超灵敏地直接从淋巴细胞中提取的人类基因组 DNA 检测(绕过 PCR 扩增)。为了实现 DNA 检测,首次应用了一种经过合理选择的星形纳米粒子(NP),即金纳米星(AuNS),用于基于选择性捕获特定 DNA 靶标并通过与 AuNS 连接的二次 DNA 探针进行信号放大的夹心样测定。等离子体模式、尺寸和在星尖的电场增强有助于最大化 LSP 和 SP 之间的等离子体耦合,以实现分析信号放大。该系统首先使用短的合成 DNA 靶序列进行测试,并应用于 DNA 生物传感,将检测限从 6.1 nM(无 NSs 标记)降低到 10 pM(有 NSs 标记)。然后将生物传感器应用于从人类淋巴细胞中提取的基因组 DNA 样本,仅经过简单的超声破碎,将检测限从 3.0 fM(无 NSs 标记)降低到 6.9 aM(有 NSs 标记)。通过对该测定进行优化,我们证明了通过与纳米粒子连接的 DNA 来调整 NSs 表面覆盖率不仅对于信号的增加而且对于生物传感器的再生/可重复使用性至关重要,可以进行数十次测量循环。