Chanyoung Noh, Taebin Yun, Minseo Kang, Kyubong Jo
Direct mapping of protein positions along long, stretched DNA molecules requires simultaneous visualization of the DNA backbone and associated protein signals. We recently established a heavy-metal- and polymer-assisted scanning electron microscopy (SEM) approach for imaging stretched DNA molecules and associated protein signals on silicon wafers. Here, we present a practical protocol for implementing this workflow using λ DNA and streptavidin-fluorescent protein-labeled λ DNA as model DNA samples. The protocol encompasses silicon wafer preparation, microchannel-guided DNA deposition, heavy-metal staining with UranyLess, polyvinylpyrrolidone (PVP) treatment of the deposited DNA sample, SEM imaging, and image analysis. UranyLess provides heavy-metal staining to enhance SEM contrast, whereas the PVP concentration modulates the relative visibility of DNA backbones and protein-associated signals. Low-PVP conditions facilitate protein-signal visualization, while high-PVP conditions enhance DNA-backbone imaging. We also describe optional in-channel and droplet-based methods for delivering UranyLess and PVP. Finally, the protocol covers DNA backbone tracing, intensity-profile analysis, and machine-learning-based determination of protein positions from SEM images. Representative dCas9-bound DNA samples further demonstrate the applicability of the workflow to different protein-binding patterns, including closely spaced binding across a repetitive target array and localized binding on genomic DNA. This workflow provides a practical framework for preparing stretched DNA samples on silicon wafers and analyzing DNA backbones and associated protein signals by SEM.