Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, Canada.
Bioconjug Chem. 2010 Aug 18;21(8):1413-6. doi: 10.1021/bc100160k.
A straightforward strategy to stably anchor one or more gold nanoparticles (AuNPs) at both the internal and terminal positions of single-stranded DNA is presented. Discrete DNA-AuNP conjugates are isolated using a noncovalent extension strand strategy, that helps to resolve prepared species by agarose gel electrophoresis (AGE). These are used to assemble well-defined AuNP squares and rectangles. Two complementary bis-AuNP-labeled DNA conjugates are then prepared. One of these places two smaller (5 nm) AuNPs at defined internal positions within a DNA strand, and the other places two larger (13 nm) AuNPs at each of its terminal positions. We show the self-assembly of these bis-AuNP conjugates into a tapered tetrameric gold nanoparticle "antenna" structures of direct relevance to engineered "hot spots" and surface enhanced Raman scattering (SERS) substrates.
本文提出了一种将一个或多个金纳米粒子(AuNPs)稳定地锚定在单链 DNA 的内部和末端位置的直接策略。使用非共价延伸链策略分离离散的 DNA-AuNP 缀合物,这有助于通过琼脂糖凝胶电泳(AGE)解析制备的物种。这些用于组装具有明确定义的 AuNP 正方形和矩形。然后制备两个互补的双 AuNP 标记的 DNA 缀合物。其中之一在 DNA 链内的定义内部位置放置两个较小的(5nm)AuNPs,另一个在每个末端位置放置两个较大的(13nm)AuNPs。我们展示了这些双 AuNP 缀合物自组装成锥形四聚体金纳米粒子“天线”结构,这些结构与工程“热点”和表面增强拉曼散射(SERS)基底直接相关。