Correlating DNA-PAINT and single-molecule FRET for multiplexed super-resolution imaging

被引:3
作者
Deussner-Helfmann, Nina S. [1 ]
Auer, Alexander [2 ,3 ,4 ]
Strauss, Maximilian T. [2 ,3 ,4 ]
Donlin-Asp, Paul [5 ]
Malkusch, Sebastian [1 ]
Dietz, Marina S. [1 ]
Barth, Hans-Dieter [1 ]
Schuman, Erin [5 ]
Jungmann, Ralf [2 ,3 ,4 ]
Heilemann, Mike [1 ]
机构
[1] Goethe Univ Frankfurt, Inst Phys & Theoret Chem, Frankfurt, Germany
[2] Ludwig Maximilians Univ Munchen, Dept Phys, Munich, Germany
[3] Ludwig Maximilians Univ Munchen, Ctr Nanosci, Munich, Germany
[4] Max Planck Inst Biochem, Martinsried, Germany
[5] Max Planck Inst Brain Res, Frankfurt, Germany
来源
SINGLE MOLECULE SPECTROSCOPY AND SUPERRESOLUTION IMAGING XIII | 2020年 / 11246卷
关键词
Single-molecule FRET; DNA-PAINT; super-resolution microscopy; DNA origami; multiplexing; LOCALIZATION MICROSCOPY; RESOLUTION; BINDING;
D O I
10.1117/12.2550629
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Correlating DNA-PAINT (point accumulation for imaging in nanoscale topography) and single-molecule FRET (Forster resonance energy transfer) enables the multiplexed detection with sub-diffraction optical resolution. We designed pairs of short oligonucleotides, labeled with donor and acceptor fluorophores with various distances generating different FRET efficiencies. The strands can transiently bind to a target docking strand, simultaneous binding of both strands results in FRET signals which yield a super-resolved image via DNA-PAINT imaging. We demonstrate FRET-PAINT by designing and imaging DNA origami, which is a useful tool to establish super-resolution methods. The DNA origami structures were equipped with three target binding sites spaced by 55 nm, a sub-diffraction limited distance, however ensuring that no FRET between the target sites occurs. We resolved the individual binding sites in the donor and acceptor channels, and in addition extracted the FRET efficiency for each site in single and mixed populations. The combination of FRET and DNA-PAINT allows for multiplexed super-resolution imaging in conjunction with distance-sensitive readout in the 1 to 10 nm range.
引用
收藏
页数:7
相关论文
共 18 条
[1]   Fast, Background-Free DNA-PAINT Imaging Using FRET-Based Probes [J].
Auer, Alexander ;
Strauss, Maximilian T. ;
Schlichthaerle, Thomas ;
Jungmann, Ralf .
NANO LETTERS, 2017, 17 (10) :6428-6434
[2]   Imaging intracellular fluorescent proteins at nanometer resolution [J].
Betzig, Eric ;
Patterson, George H. ;
Sougrat, Rachid ;
Lindwasser, O. Wolf ;
Olenych, Scott ;
Bonifacino, Juan S. ;
Davidson, Michael W. ;
Lippincott-Schwartz, Jennifer ;
Hess, Harald F. .
SCIENCE, 2006, 313 (5793) :1642-1645
[3]   Super-resolution imaging and estimation of protein copy numbers at single synapses with DNA-PAINT [J].
Boeger, Carolin ;
Hafner, Anne-Sophie ;
Schlichthaerle, Thomas ;
Strauss, Maximilian T. ;
Malkusch, Sebastian ;
Endesfelder, Ulrike ;
Jungmann, Ralf ;
Schuman, Erin M. ;
Heilemann, Mike .
NEUROPHOTONICS, 2019, 6 (03)
[4]   Surface Passivation for Single-molecule Protein Studies [J].
Chandradoss, Stanley D. ;
Haagsma, Anna C. ;
Lee, Young Kwang ;
Hwang, Jae-Ho ;
Nam, Jwa-Min ;
Joo, Chirlmin .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2014, (86)
[5]   Correlative Single-Molecule FRET and DNA-PAINT Imaging [J].
Deussner-Helfmann, Nina S. ;
Auer, Alexander ;
Strauss, Maximilian T. ;
Malkusch, Sebastian ;
Dietz, Marina S. ;
Barth, Hans -Dieter ;
Jungmann, Ralf ;
Heilemann, Mike .
NANO LETTERS, 2018, 18 (07) :4626-4630
[6]   Competitive Binding Study Revealing the Influence of Fluorophore Labels on Biomolecular Interactions [J].
Dietz, Marina S. ;
Wehrheim, S. Sophia ;
Harwardt, Marie-Lena I. E. ;
Niemann, Hartmut H. ;
Heilemann, Mike .
NANO LETTERS, 2019, 19 (11) :8245-8249
[7]   Optical super-resolution microscopy unravels the molecular composition of functional protein complexes [J].
Dietz, Marina S. ;
Heilemann, Mike .
NANOSCALE, 2019, 11 (39) :17981-17991
[8]   A simple method to estimate the average localization precision of a single-molecule localization microscopy experiment [J].
Endesfelder, Ulrike ;
Malkusch, Sebastian ;
Fricke, Franziska ;
Heilemann, Mike .
HISTOCHEMISTRY AND CELL BIOLOGY, 2014, 141 (06) :629-638
[9]   Single-molecule localization microscopy - near-molecular spatial resolution in light microscopy with photoswitchable fluorophores [J].
Fuerstenberg, Alexandre ;
Heilemann, Mike .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (36) :14919-14930
[10]   Subdiffraction-resolution fluorescence imaging with conventional fluorescent probes [J].
Heilemann, Mike ;
van de Linde, Sebastian ;
Schuttpelz, Mark ;
Kasper, Robert ;
Seefeldt, Britta ;
Mukherjee, Anindita ;
Tinnefeld, Philip ;
Sauer, Markus .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (33) :6172-6176