Protocol for SUM-PAINT spatial proteomic imaging generating neuronal architecture maps in rat hippocampal neurons

To unravel the complexity of biological processes, it is necessary to resolve the underlying protein organization down to single proteins. Here, we present a protocol for secondary label-based unlimited multiplexed DNA-PAINT (SUM-PAINT), a DNA-PAINT-based super-resolution microscopy technique that is capable of resolving virtually unlimited protein species with single-protein resolution. We describe the steps to prepare neuronal cultures, troubleshoot and conduct SUM-PAINT experiments, and analyze the resulting feature-rich neuronal cell atlases using unsupervised machine learning approaches. For complete details on the use and execution of this protocol, please refer to Unterauer et al.<sup>1</sup>.

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Publication Details

Journal
STAR Protocols
Published
2025-03-01
DOI
https://doi.org/10.1016/j.xpro.2025.103637
Citations
1
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
1.63
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article

Protocol for SUM-PAINT spatial proteomic imaging generating neuronal architecture maps in rat hippocampal neurons

Eduard M. Unterauer, Eva-Maria Schentarra, Sayedali Shetab Boushehri, Eugenio F. Fornasiero et al.
1 citations
STAR Protocols
Advanced Fluorescence Microscopy Techniques
1.63
article

Protocol for SUM-PAINT spatial proteomic imaging generating neuronal architecture maps in rat hippocampal neurons

Eduard M. Unterauer, Eva-Maria Schentarra, Sayedali Shetab Boushehri, Eugenio F. Fornasiero, Carsten Marr, Ralf Jungmann, Kristina Jevdokimenko, Felipe Opazo
article en
1 citations

Abstract

To unravel the complexity of biological processes, it is necessary to resolve the underlying protein organization down to single proteins. Here, we present a protocol for secondary label-based unlimited multiplexed DNA-PAINT (SUM-PAINT), a DNA-PAINT-based super-resolution microscopy technique that is capable of resolving virtually unlimited protein species with single-protein resolution. We describe the steps to prepare neuronal cultures, troubleshoot and conduct SUM-PAINT experiments, and analyze the resulting feature-rich neuronal cell atlases using unsupervised machine learning approaches. For complete details on the use and execution of this protocol, please refer to Unterauer et al.<sup>1</sup>.

STAR ProtocolsVol. 6(1)
University of Trieste (IT), Center for NanoScience (DE), Helmholtz Zentrum München (DE), Universitätsmedizin Göttingen (DE), Max Planck Institute of Biochemistry (DE), University of Göttingen (DE), Ludwig-Maximilians-Universität München (DE)
Openalex Percentile: Top 16%
Advanced Fluorescence Microscopy Techniques
1.63
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Protocol for SUM-PAINT spatial proteomic imaging generating neuronal architecture maps in rat hippocampal neurons — Eduard M. Unterauer, Eva-Maria Schentarra, et al. · STAR Protocols (2025) | TGRS Research Map | TGRS