Department of Cell Biology, Yale University, New Haven, CT, USA.
Nanobiology Institute, Yale University, West Haven, CT, USA.
Nat Methods. 2022 May;19(5):554-559. doi: 10.1038/s41592-022-01464-9. Epub 2022 May 2.
DNA-based points accumulation for imaging in nanoscale topography (DNA-PAINT) is a powerful super-resolution microscopy method that can acquire high-fidelity images at nanometer resolution. It suffers, however, from high background and slow imaging speed, both of which can be attributed to the presence of unbound fluorophores in solution. Here we present two-color fluorogenic DNA-PAINT, which uses improved imager probe and docking strand designs to solve these problems. These self-quenching single-stranded DNA probes are conjugated with a fluorophore and quencher at the terminals, which permits an increase in fluorescence by up to 57-fold upon binding and unquenching. In addition, the engineering of base pair mismatches between the fluorogenic imager probes and docking strands allowed us to achieve both high fluorogenicity and the fast binding kinetics required for fast imaging. We demonstrate a 26-fold increase in imaging speed over regular DNA-PAINT and show that our new implementation enables three-dimensional super-resolution DNA-PAINT imaging without optical sectioning.
基于 DNA 的点积累用于纳米形貌成像(DNA-PAINT)是一种强大的超分辨率显微镜方法,可在纳米分辨率下获得高保真度的图像。然而,它存在高背景和成像速度慢的问题,这两者都可以归因于溶液中未结合的荧光团的存在。在这里,我们提出了双色荧光 DNA-PAINT,它使用改进的成像探针和对接链设计来解决这些问题。这些自猝灭的单链 DNA 探针在末端连接有荧光团和猝灭剂,使得结合和解猝灭后荧光可增强高达 57 倍。此外,在荧光成像探针和对接链之间设计碱基对错配,使我们能够实现高荧光性和快速成像所需的快速结合动力学。我们证明了成像速度比常规 DNA-PAINT 提高了 26 倍,并表明我们的新方法能够实现无需光学切片的三维超分辨率 DNA-PAINT 成像。