Single-Molecule Kinetics and Super-Resolution Microscopy by Fluorescence Imaging of Transient Binding on DNA Origami

被引:651
作者
Jungmann, Ralf [1 ,2 ,3 ]
Steinhauer, Christian [1 ,3 ]
Scheible, Max [2 ]
Kuzyk, Anton [2 ]
Tinnefeld, Philip [1 ,3 ]
Simmel, Friedrich C. [1 ,2 ]
机构
[1] Univ Munich, Ctr NanoSci, D-80799 Munich, Germany
[2] Tech Univ Munich, Dept Phys, Lehrstuhl Bioelekt, D-85748 Garching, Germany
[3] Tech Univ Carolo Wilhelmina Braunschweig, D-38106 Braunschweig, Germany
关键词
Nanobiotechnology; biophysics; DNA origami; fluorescence microscopy; super-resolution; single-molecule kinetics; HYBRIDIZATION; RESOLUTION;
D O I
10.1021/nl103427w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DNA origami is a powerful method for the programmable assembly of nanoscale molecular structures. For applications of these structures as functional biomaterials, the study of reaction kinetics and dynamic processes in real time and with high spatial resolution becomes increasingly important. We present a single-molecule assay For the study of binding and unbinding kinetics on DNA origami. We find that the kinetics of hybridization to single-stranded extensions on DNA origami is similar to isolated substrate-immobilized DNA with a slight position dependence on the origami. On the basis of the knowledge of the kinetics, we exploit reversible specific binding of labeled oligonucleotides to DNA nanostructures for PAINT (points accumulation for imaging in nanoscale topography) imaging with <30 nm resolution. The method is demonstrated For flat monomeric DNA structures as well as multimeric, ribbon-like DNA structures.
引用
收藏
页码:4756 / 4761
页数:6
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