Department of Physics, University of Illinois at Urbana-Champaign, Urbana, 61801, USA.
Center for the Physics of the Living Cell, University of Illinois at Urbana-Champaign, Urbana, 61801, USA.
Small Methods. 2023 Apr;7(4):e2201181. doi: 10.1002/smtd.202201181. Epub 2023 Feb 3.
Point accumulation for imaging in nanoscale topography (PAINT) is a single-molecule technique for super-resolution microscopy, which uses exchangeable single stranded DNA oligos or peptide-pairs to create blinking phenomenon and achieves ≈5-25 nanometer resolution. Here, it is shown that by transfecting the protein-of-interest with a docker-coil, rather than by adding the docker externally-as is the norm when using DNA tethers or antibodies as dockers-similar localization can be achieved, ≈10 nm. However, using a transfected docker has several experimental advances and simplifications. Most importantly, it allows Peptide-PAINT to be applied to transfected live cells for imaging surface proteins in mammalian cells and neurons under physiological conditions. The enhanced resolution of Peptide-PAINT is also shown for organelles in fixed cells to unravel structural details including ≈40-nm and ≈60-nm axial repeats in vimentin filaments in the cytoplasm, and fiber shapes of sub-100-nm histone-rich regions in the nucleus.
用于纳米级形貌成像的点累积(PAINT)是一种单分子超分辨率显微镜技术,它使用可交换的单链 DNA 寡核苷酸或肽对来产生闪烁现象,并实现 ≈5-25 纳米的分辨率。在这里,我们展示了通过转染与 docker-coil 的目的蛋白,而不是像使用 DNA 系链或抗体作为 dockers 时那样通过外部添加 docker 来实现类似的定位,≈10nm。然而,使用转染的 docker 具有几个实验上的改进和简化。最重要的是,它允许 Peptide-PAINT 应用于转染的活细胞,以在生理条件下对哺乳动物细胞和神经元表面蛋白进行成像。固定细胞中细胞器的分辨率也得到了提高,以揭示结构细节,包括细胞质中纤维蛋白丝中的 ≈40nm 和 ≈60nm 轴向重复,以及核中富含组蛋白的亚 100nm 纤维形状。