Phospho-seq: integrated, multi-modal profiling of intracellular protein dynamics in single cells

Cell signaling plays a critical role in neurodevelopment, regulating cellular behavior and fate. While multimodal single-cell sequencing technologies are rapidly advancing, scalable and flexible profiling of cell signaling states alongside other molecular modalities remains challenging. Here we present Phospho-seq, an integrated approach that aims to quantify cytoplasmic and nuclear proteins, including those with post-translational modifications, and to connect their activity with cis-regulatory elements and transcriptional targets. We utilize a simplified benchtop antibody conjugation method to create large custom neuro-focused antibody panels for simultaneous protein and scATAC-seq profiling on whole cells, alongside both experimental and computational strategies to incorporate transcriptomic measurements. We apply our workflow to cell lines, induced pluripotent stem cells, and months-old retinal and brain organoids to demonstrate its broad applicability. We show that Phospho-seq can provide insights into cellular states and trajectories, shed light on gene regulatory relationships, and help explore the causes and effects of diverse cell signaling in neurodevelopment.

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Publication Details

Journal
Nature Communications
Published
2025-02-04
DOI
https://doi.org/10.1038/s41467-025-56590-7
Citations
5
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
4.03
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article

Phospho-seq: integrated, multi-modal profiling of intracellular protein dynamics in single cells

Austin Hartman, Philipp Wahle, Barbara Treutlein, Fides Zenk et al.
5 citations
Nature Communications
Single-cell and spatial transcriptomics
4.03
article

Phospho-seq: integrated, multi-modal profiling of intracellular protein dynamics in single cells

Austin Hartman, Philipp Wahle, Barbara Treutlein, Fides Zenk, Giovanna Brancati, Carol Dalgarno, John D. Blair, Rahul Satija
article en
5 citations

Abstract

Cell signaling plays a critical role in neurodevelopment, regulating cellular behavior and fate. While multimodal single-cell sequencing technologies are rapidly advancing, scalable and flexible profiling of cell signaling states alongside other molecular modalities remains challenging. Here we present Phospho-seq, an integrated approach that aims to quantify cytoplasmic and nuclear proteins, including those with post-translational modifications, and to connect their activity with cis-regulatory elements and transcriptional targets. We utilize a simplified benchtop antibody conjugation method to create large custom neuro-focused antibody panels for simultaneous protein and scATAC-seq profiling on whole cells, alongside both experimental and computational strategies to incorporate transcriptomic measurements. We apply our workflow to cell lines, induced pluripotent stem cells, and months-old retinal and brain organoids to demonstrate its broad applicability. We show that Phospho-seq can provide insights into cellular states and trajectories, shed light on gene regulatory relationships, and help explore the causes and effects of diverse cell signaling in neurodevelopment.

Nature CommunicationsVol. 16(1)
ETH Zurich (CH), New York Genome Center (US), New York University (US)
Openalex Percentile: Top 7%
Single-cell and spatial transcriptomics
4.03
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Phospho-seq: integrated, multi-modal profiling of intracellular protein dynamics in single cells — Austin Hartman, Philipp Wahle, et al. · Nature Communications (2025) | TGRS Research Map | TGRS