Jakobsen Ulla, Simonsen Adam C, Vogel Stefan
Department of Physics and Chemistry, University of Southern Denmark, Nucleic Acid Center, Campusvej 55, 5230 Odense, Denmark.
J Am Chem Soc. 2008 Aug 13;130(32):10462-3. doi: 10.1021/ja8030054. Epub 2008 Jul 22.
Immobilization of DNA (encoding) on solid nanoparticles requires surface chemistry, which is well established for gold surfaces but often tedious and not generally applicable for many other inorganic surface materials. While substantial effort has been devoted to expanding surface chemistry techniques for solid nanoparticles, considerably less attention has been given to the development of noncovalent attachment of DNA to soft nanoparticles, like liposomes. Here we report a DNA-controlled assembly of liposomes in solution and on solid supported membranes, this process displays remarkably sharp thermal transitions from an assembled to a disassembled state, allowing application of DNA-controlled liposome assembly for the detection of polynucleotides (e.g., DNA) with single mismatch discrimination power. The method is based on a single DNA strand (contains two lipid membrane anchors), which is able to noncovalently attach to a liposome surface. This design enables detection of biological polynucleotide targets as the complementary strand can be unmodified DNA and RNA strands.
将(编码)DNA固定在固体纳米颗粒上需要表面化学技术,这在金表面已经成熟,但通常很繁琐,且不适用于许多其他无机表面材料。尽管人们在扩展固体纳米颗粒的表面化学技术方面付出了巨大努力,但对于DNA与软纳米颗粒(如脂质体)的非共价连接的开发关注较少。在此,我们报道了脂质体在溶液中和固体支持膜上的DNA控制组装,该过程显示出从组装状态到解体状态的明显尖锐热转变,从而使得DNA控制的脂质体组装可用于具有单碱基错配识别能力的多核苷酸(如DNA)检测。该方法基于一条单链DNA(包含两个脂质膜锚定基团),它能够非共价地附着在脂质体表面。这种设计能够检测生物多核苷酸靶标,因为互补链可以是未修饰的DNA和RNA链。