Multimodal chromatin profiling using nanobody-based single-cell CUT&Tag

Probing histone modifications at a single-cell level in thousands of cells has been enabled by technologies such as single-cell CUT&Tag. Here we describe nano-CUT&Tag (nano-CT), which allows simultaneous mapping of up to three epigenomic modalities at single-cell resolution using nanobody-Tn5 fusion proteins. Multimodal nano-CT is compatible with starting materials as low as 25,000-200,000 cells and has significantly higher sensitivity and number of fragments per cell than single-cell CUT&Tag. We use nano-CT to simultaneously profile chromatin accessibility, H3K27ac, and H3K27me3 in juvenile mouse brain, allowing for discrimination of more cell types and states than unimodal single-cell CUT&Tag. We also infer chromatin velocity between assay for transposase-accessible chromatin (ATAC) and H3K27ac in the oligodendrocyte lineage and deconvolute H3K27me3 repressive states, finding two sequential waves of H3K27me3 repression at distinct gene modules during oligodendrocyte lineage progression. Given its high resolution, versatility, and multimodal features, nano-CT allows unique insights in epigenetic landscapes in complex biological systems at the single-cell level. Three epigenetic features are mapped at single-cell resolution using Tn5-nanobody fusion proteins

Automated summary

The nano-CUT&Tag (nano-CT) technique enables the mapping of three epigenetic features at single-cell resolution using nanobody-Tn5 fusion proteins. It has higher sensitivity and more fragments per cell compared to single-cell CUT&Tag, allowing for better discrimination of cell types and states. Nano-CT provides unique insights into epigenetic landscapes in complex biological systems at the single-cell level.