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相关单分子 FRET 和 DNA-PAINT 成像。

Correlative Single-Molecule FRET and DNA-PAINT Imaging.

机构信息

Single Molecule Biophysics, Institute of Physical and Theoretical Chemistry , Goethe-University Frankfurt , Max-von-Laue-Strasse 7 , 60438 Frankfurt , Germany.

Department of Physics and Center for Nanoscience , Ludwig Maximilian University , 80539 Munich , Germany.

出版信息

Nano Lett. 2018 Jul 11;18(7):4626-4630. doi: 10.1021/acs.nanolett.8b02185. Epub 2018 Jun 29.

Abstract

DNA-PAINT is an optical super-resolution microscopy method that can visualize nanoscale protein arrangements and provide spectrally unlimited multiplexing capabilities. However, current multiplexing implementations based on, for example, DNA exchange (such as Exchange-PAINT) achieves multitarget detection by sequential imaging, limiting throughput. Here, we combine DNA-PAINT with single-molecule FRET and use the FRET efficiency as parameter for multiplexed imaging with high specificity. We demonstrate correlated single-molecule FRET and super-resolution on DNA origami structures, which are equipped with binding sequences that are targeted by pairs of dye-labeled oligonucleotides generating the FRET signal. We futher extract FRET values from single binding sites that are spaced just ∼55 nm apart, demonstrating super-resolution FRET imaging. This combination of FRET and DNA-PAINT allows for multiplexed super-resolution imaging with low background and opens the door for accurate distance readout in the 1-10 nm range.

摘要

DNA-PAINT 是一种光学超分辨率显微镜方法,可以可视化纳米级蛋白质排列,并提供光谱上无限的多重标记能力。然而,目前基于 DNA 交换的多重标记实现(如 Exchange-PAINT)通过顺序成像实现多目标检测,限制了通量。在这里,我们将 DNA-PAINT 与单分子 FRET 结合,并使用 FRET 效率作为高特异性多重标记成像的参数。我们在 DNA 折纸结构上演示了相关的单分子 FRET 和超分辨率,这些结构配备了结合序列,这些结合序列被靶向一对用染料标记的寡核苷酸,产生 FRET 信号。我们进一步从仅相隔约 55nm 的单个结合位点中提取 FRET 值,证明了超分辨率 FRET 成像。FRET 和 DNA-PAINT 的这种组合允许进行具有低背景的多重超分辨率成像,并为在 1-10nm 范围内进行准确的距离读出开辟了道路。

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