Protocol for simultaneous detection of mRNAs and (phospho-)proteins with ARTseq-FISH in mouse embryonic stem cells

Understanding the molecular signatures of individual cells within complex biological systems is crucial for deciphering cellular heterogeneity and uncovering regulatory mechanisms. Here, we present a protocol for simultaneous multiplexed detection of selected mRNAs and (phospho-)proteins in mouse embryonic stem cells using spatial single-cell profiling. We describe steps for employing single-stranded DNA (ssDNA)-labeled antibo'dies, padlock probes, and rolling circle amplification to achieve simultaneous visualization of mRNAs and (phospho-)proteins at subcellular resolution. This protocol has potential application in identifying cells in heterogeneous biological microenvironments. For complete details on the use and execution of this protocol, please refer to Hu et al.<sup>1</sup>.

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Publication Details

Journal
STAR Protocols
Published
2024-10-01
DOI
https://doi.org/10.1016/j.xpro.2024.103336
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.23

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article

Protocol for simultaneous detection of mRNAs and (phospho-)proteins with ARTseq-FISH in mouse embryonic stem cells

Maike M. K. Hansen, Óscar García‐Blay, Wilhelm T. S. Huck, Xinyu Hu et al.
1 citations
STAR Protocols
Single-cell and spatial transcriptomics
0.23
article

Protocol for simultaneous detection of mRNAs and (phospho-)proteins with ARTseq-FISH in mouse embryonic stem cells

Maike M. K. Hansen, Óscar García‐Blay, Wilhelm T. S. Huck, Xinyu Hu, Bob van Sluijs
article en
1 citations

Abstract

Understanding the molecular signatures of individual cells within complex biological systems is crucial for deciphering cellular heterogeneity and uncovering regulatory mechanisms. Here, we present a protocol for simultaneous multiplexed detection of selected mRNAs and (phospho-)proteins in mouse embryonic stem cells using spatial single-cell profiling. We describe steps for employing single-stranded DNA (ssDNA)-labeled antibo'dies, padlock probes, and rolling circle amplification to achieve simultaneous visualization of mRNAs and (phospho-)proteins at subcellular resolution. This protocol has potential application in identifying cells in heterogeneous biological microenvironments. For complete details on the use and execution of this protocol, please refer to Hu et al.<sup>1</sup>.

STAR ProtocolsVol. 5(4)
HAN University of Applied Sciences (NL), Radboud University Nijmegen (NL)
European Commission, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, China Scholarship Council, KWF Kankerbestrijding, Radboud Universitair Medisch Centrum, Oncode Institute, European Research Council, H2020 European Research Council
Life below water
Openalex Percentile: Top 42%
Single-cell and spatial transcriptomics
0.23
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