Kukolka Florian, Müller Barbara K, Paternoster Stefan, Arndt Andreas, Niemeyer Christof M, Bräuchle Christoph, Lamb Don C
Fachbereich Chemie Biologisch-Chemische Mikrostrukturtechnik, Universität Dortmund, Otto-Hahn-Strasse 6, 44227 Dortmund, Germany.
Small. 2006 Aug;2(8-9):1083-9. doi: 10.1002/smll.200600202.
The development of nanobiotechnological devices requires the ability to build various components with nanometer accuracy. DNA is a well-established nanoscale building block that self assembles due to specific interactions that are encoded in its sequence. Recently, it has become possible to couple proteins to DNA, thereby expanding the capabilities of DNA for use with molecular photonics and bioelectronics. Here, we present the design and characterization of a supramolecular Förster resonance energy transfer (FRET) system by using a fluorescent protein bound to single-stranded DNA (ssDNA), a fluorophore attached to a second ssDNA molecule, and a complementary strand for hybridizing the two fluorophores together. The FRET efficiency was studied by using both ensemble and single-pair FRET measurements. The distance between the two fluorophores was determined from the single-pair FRET efficiency and could be described by a simple cylindrical model for the DNA. Hence, DNA can be used as a scaffold for positioning fluorescent proteins, as well as traditional fluorophores, with nanometer accuracy and shows great potential for use in the future of nanobiotechnology.
纳米生物技术设备的发展需要具备以纳米精度构建各种组件的能力。DNA是一种成熟的纳米级构建模块,由于其序列中编码的特定相互作用而能自我组装。最近,已能够将蛋白质与DNA偶联,从而扩展了DNA在分子光子学和生物电子学方面的应用能力。在此,我们展示了一种超分子Förster共振能量转移(FRET)系统的设计与表征,该系统使用与单链DNA(ssDNA)结合的荧光蛋白、连接到第二个ssDNA分子上的荧光团以及用于将两个荧光团杂交在一起的互补链。通过使用整体FRET测量和单对FRET测量来研究FRET效率。根据单对FRET效率确定了两个荧光团之间的距离,并且该距离可以用一个简单的DNA圆柱形模型来描述。因此,DNA可用作支架,以纳米精度定位荧光蛋白以及传统荧光团,并且在未来的纳米生物技术中显示出巨大的应用潜力。