Fraunhofer Institute for Biomedical Engineering, Branch Potsdam-Golm, Department of Nanobiotechnology & Nanomedicine ,Am Mühlenberg 13, 14476 Potsdam, Germany.
Small. 2009 Oct;5(20):2316-22. doi: 10.1002/smll.200900319.
Enzymatic isothermal rolling circle amplification (RCA) produces long concatemeric single-stranded DNA (ssDNA) molecules if a small circular ssDNA molecule is applied as the template. A method is presented here in which the RCA reaction is carried out in a flow-through system, starting from isolated surface-tethered DNA primers. This approach combines gentle fluidic handling of the single-stranded RCA products, such as staining or stretching via a receding meniscus, with the option of simultaneous (fluorescence) microscopic observation. It is shown that the stretched and surface-attached RCA products are accessible for hybridization of complementary oligonucleotides, which demonstrates their addressability by complementary base pairing. The long RCA products should be well suited to bridge the gap between biomolecular nanoscale building-blocks and structures at the micro- and macroscale, especially at the single-molecule level presented here.
酶促等温滚环扩增(RCA)如果以小的环状单链 DNA (ssDNA)分子作为模板,就会产生长的串联的单链 DNA 分子。本文提出了一种在流动系统中进行 RCA 反应的方法,从分离的表面固定化 DNA 引物开始。这种方法将温和的流体处理单链 RCA 产物(例如,通过后退的弯月面进行染色或拉伸)与同时进行(荧光)显微镜观察的功能相结合。结果表明,拉伸和表面附着的 RCA 产物可用于互补寡核苷酸的杂交,这证明了它们通过互补碱基配对的可寻址性。长的 RCA 产物应该非常适合桥接生物分子纳米级构建块与微尺度和宏观尺度结构之间的差距,特别是在本文中呈现的单分子水平上。