Stein Johannes, Ericsson Maria, Nofal Michel, Magni Lorenzo, Aufmkolk Sarah, McMillan Ryan B, Breimann Laura, Herlihy Conor P, Lee S Dean, Willemin Andréa, Wohlmann Jens, Arguedas-Jimenez Laura, Yin Peng, Pombo Ana, Church George M, Wu Chao-Ting
Wyss Institute of Biologically Inspired Engineering, Boston, MA, USA.
Department of Genetics, Harvard Medical School, Boston, MA, USA.
bioRxiv. 2025 Feb 13:2024.02.05.576943. doi: 10.1101/2024.02.05.576943.
DNA-PAINT enables nanoscale imaging with virtually unlimited multiplexing and molecular counting. Here, we address challenges, such as variable imaging performance and target accessibility, that can limit its broader applicability. Specifically, we enhance its capacity for robust single-protein imaging and molecular counting by optimizing the integration of TIRF microscopy with physical sectioning, in particular, Tokuyasu cryosectioning. Our method, tomographic & kinetically enhanced DNA-PAINT (tkPAINT), achieves 3 nm localization precision across diverse samples, enhanced imager binding, and improved cellular integrity. tkPAINT can facilitate molecular counting with DNA-PAINT inside the nucleus, as demonstrated through its quantification of the in situ abundance of RNA Polymerase II in both HeLa cells as well as mouse tissues. Anticipating that tkPAINT could become a versatile tool for the exploration of biomolecular organization and interactions across cells and tissues, we also demonstrate its capacity to support multiplexing, multimodal targeting of proteins and nucleic acids, and 3D imaging.
DNA-PAINT技术能够实现具有几乎无限复用性和分子计数功能的纳米级成像。在此,我们应对了一些可能限制其更广泛应用的挑战,如成像性能的变化和靶点可及性。具体而言,我们通过优化全内反射荧光显微镜(TIRF)与物理切片(特别是Tokuyasu冷冻切片)的整合,增强了其对单个蛋白质进行稳健成像和分子计数的能力。我们的方法——断层扫描与动力学增强DNA-PAINT(tkPAINT),在各种样本中实现了3纳米的定位精度,增强了成像剂结合,并改善了细胞完整性。tkPAINT能够促进在细胞核内使用DNA-PAINT进行分子计数,通过对HeLa细胞和小鼠组织中RNA聚合酶II的原位丰度进行定量分析得到了证明。预计tkPAINT可能成为探索细胞和组织中生物分子组织及相互作用的通用工具,我们还展示了它支持复用、蛋白质和核酸的多模态靶向以及三维成像的能力。