All Probes Plasmids (APPs) for multicolor and long-term tracking of single-mRNA translation dynamics

Live-cell single-mRNA imaging of translation is inherently challenging, demanding precise optimization of multiple imaging components. To simplify these experiments, we developed All Probes Plasmids (APPs)-a panel of plasmids encoding all the necessary probes for imaging at optimized relative expression levels. APPs incorporate widely used translation tags, fluorescent proteins, and mRNA labeling systems, streamlining both multiplexed imaging and reporter immobilization. By cotransfecting just two plasmids-a reporter and an APP-individual translation sites can be visualized in living cells with high signal-to-noise. We demonstrate how APPs facilitate high-fidelity multicolor translation imaging, long-term single-mRNA tracking, and fluorescence correlation spectroscopy to quantify ribosome kinetics. By lowering technical barriers and enhancing experimental flexibility, APPs provide a versatile platform for advancing single-mRNA translation research in living cells.

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Publication Details

Journal
Molecular Biology of the Cell
Published
2025-05-14
DOI
https://doi.org/10.1091/mbc.e25-02-0091
Citations
2
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
1.61
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All Probes Plasmids (APPs) for multicolor and long-term tracking of single-mRNA translation dynamics

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article

All Probes Plasmids (APPs) for multicolor and long-term tracking of single-mRNA translation dynamics

Agustín B. de Heredia, Tatsuya Morisaki, Gabriel Galindo, Timothy J. Stasevich, Gretchen M. Fixen
article en
2 citations

Abstract

Live-cell single-mRNA imaging of translation is inherently challenging, demanding precise optimization of multiple imaging components. To simplify these experiments, we developed All Probes Plasmids (APPs)-a panel of plasmids encoding all the necessary probes for imaging at optimized relative expression levels. APPs incorporate widely used translation tags, fluorescent proteins, and mRNA labeling systems, streamlining both multiplexed imaging and reporter immobilization. By cotransfecting just two plasmids-a reporter and an APP-individual translation sites can be visualized in living cells with high signal-to-noise. We demonstrate how APPs facilitate high-fidelity multicolor translation imaging, long-term single-mRNA tracking, and fluorescence correlation spectroscopy to quantify ribosome kinetics. By lowering technical barriers and enhancing experimental flexibility, APPs provide a versatile platform for advancing single-mRNA translation research in living cells.

Molecular Biology of the CellVol. 36(6)
Colorado State University (US)
Openalex Percentile: Top 17%
RNA and protein synthesis mechanisms
1.61
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