The <scp>IQ</scp> ‐compete assay for measuring mitochondrial protein import efficiencies in living yeast cells

Most mitochondrial proteins are synthesized in the cytosol and imported into the organelle. Here, we describe a novel Import and de-Quenching Competition (IQ-compete) assay which monitors the import efficiency of model proteins by fluorescence in living cells. For this method, the sequence of the tobacco etch virus (TEV) protease is fused to a mitochondrial precursor and coexpressed with a cytosolic reporter which becomes fluorescent upon TEV cleavage. Thus, inefficient import of the fusion protein leads to a fluorescent signal. With the IQ-compete assay, the import efficiency of proteins can be reliably analyzed in fluorescence readers, by flow cytometry, by microscopy, and by western blotting. We are convinced that the IQ-compete assay will be a powerful strategy for many different applications. Impact statement This article describes a novel method to monitor the mitochondrial import efficiency for a given protein in living yeast cells. With this IQ-compete assay, protein import efficiencies can be quantified by fluorescent microscopy, flow cytometry, fluorescence spectrometry or western blotting.

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Publication Details

Journal
FEBS Letters
Published
2025-10-25
DOI
https://doi.org/10.1002/1873-3468.70206
Citations
1
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.81

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article

The IQ ‐compete assay for measuring mitochondrial protein import efficiencies in living yeast cells

Johannes M. Herrmann, Saskia Rödl, Annika Egeler, Yasmin Hoffman
1 citations
FEBS Letters
Mitochondrial Function and Pathology
0.81
article

The IQ ‐compete assay for measuring mitochondrial protein import efficiencies in living yeast cells

Johannes M. Herrmann, Saskia Rödl, Annika Egeler, Yasmin Hoffman
article en
1 citations

Abstract

Most mitochondrial proteins are synthesized in the cytosol and imported into the organelle. Here, we describe a novel Import and de-Quenching Competition (IQ-compete) assay which monitors the import efficiency of model proteins by fluorescence in living cells. For this method, the sequence of the tobacco etch virus (TEV) protease is fused to a mitochondrial precursor and coexpressed with a cytosolic reporter which becomes fluorescent upon TEV cleavage. Thus, inefficient import of the fusion protein leads to a fluorescent signal. With the IQ-compete assay, the import efficiency of proteins can be reliably analyzed in fluorescence readers, by flow cytometry, by microscopy, and by western blotting. We are convinced that the IQ-compete assay will be a powerful strategy for many different applications. Impact statement This article describes a novel method to monitor the mitochondrial import efficiency for a given protein in living yeast cells. With this IQ-compete assay, protein import efficiencies can be quantified by fluorescent microscopy, flow cytometry, fluorescence spectrometry or western blotting.

FEBS LettersVol. 600(1)
University of Kaiserslautern (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 22%
Mitochondrial Function and Pathology
0.81
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The <scp>IQ</scp> ‐compete assay for measuring mitochondrial protein import efficiencies in living yeast cells — Johannes M. Herrmann, Saskia Rödl, et al. · FEBS Letters (2025) | TGRS Research Map | TGRS