Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast
Abstract Background Translation is an important point of regulation in protein synthesis. However, there is a limited number of methods available to measure global translation activity in yeast. Recently, O-propargyl-puromycin (OPP) labelling has been established for mammalian cells, but unmodified...
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doaj-8860b4e041724f87aa44d1d18c3938932021-04-25T11:22:30ZengBMCBMC Microbiology1471-21802021-04-0121111010.1186/s12866-021-02185-3Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeastJennifer Staudacher0Corinna Rebnegger1Brigitte Gasser2Christian Doppler Laboratory for Growth-decoupled Protein Production in Yeast, Department of Biotechnology, BOKU University of Natural Resources and Life SciencesChristian Doppler Laboratory for Growth-decoupled Protein Production in Yeast, Department of Biotechnology, BOKU University of Natural Resources and Life SciencesChristian Doppler Laboratory for Growth-decoupled Protein Production in Yeast, Department of Biotechnology, BOKU University of Natural Resources and Life SciencesAbstract Background Translation is an important point of regulation in protein synthesis. However, there is a limited number of methods available to measure global translation activity in yeast. Recently, O-propargyl-puromycin (OPP) labelling has been established for mammalian cells, but unmodified yeasts are unsusceptible to puromycin. Results We could increase susceptibility by using a Komagataella phaffii strain with an impaired ergosterol pathway (erg6Δ), but translation measurements are restricted to this strain background, which displayed growth deficits. Using surfactants, specifically Imipramine, instead, proved to be more advantageous and circumvents previous restrictions. Imipramine-supplemented OPP-labelling with subsequent flow cytometry analysis, enabled us to distinguish actively translating cells from negative controls, and to clearly quantify differences in translation activities in different strains and growth conditions. Specifically, we investigated K. phaffii at different growth rates, verified that methanol feeding alters translation activity, and analysed global translation in strains with genetically modified stress response pathways. Conclusions We set up a simple protocol to measure global translation activity in yeast on a single cell basis. The use of surfactants poses a practical and non-invasive alternative to the commonly used ergosterol pathway impaired strains and thus impacts a wide range of applications where increased drug and dye uptake is needed.https://doi.org/10.1186/s12866-021-02185-3Global translation activityKomagataella phaffii (Pichia pastoris)O-propargyl-puromycin (OPP)SurfactantStress response |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jennifer Staudacher Corinna Rebnegger Brigitte Gasser |
spellingShingle |
Jennifer Staudacher Corinna Rebnegger Brigitte Gasser Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast BMC Microbiology Global translation activity Komagataella phaffii (Pichia pastoris) O-propargyl-puromycin (OPP) Surfactant Stress response |
author_facet |
Jennifer Staudacher Corinna Rebnegger Brigitte Gasser |
author_sort |
Jennifer Staudacher |
title |
Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast |
title_short |
Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast |
title_full |
Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast |
title_fullStr |
Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast |
title_full_unstemmed |
Treatment with surfactants enables quantification of translational activity by O-propargyl-puromycin labelling in yeast |
title_sort |
treatment with surfactants enables quantification of translational activity by o-propargyl-puromycin labelling in yeast |
publisher |
BMC |
series |
BMC Microbiology |
issn |
1471-2180 |
publishDate |
2021-04-01 |
description |
Abstract Background Translation is an important point of regulation in protein synthesis. However, there is a limited number of methods available to measure global translation activity in yeast. Recently, O-propargyl-puromycin (OPP) labelling has been established for mammalian cells, but unmodified yeasts are unsusceptible to puromycin. Results We could increase susceptibility by using a Komagataella phaffii strain with an impaired ergosterol pathway (erg6Δ), but translation measurements are restricted to this strain background, which displayed growth deficits. Using surfactants, specifically Imipramine, instead, proved to be more advantageous and circumvents previous restrictions. Imipramine-supplemented OPP-labelling with subsequent flow cytometry analysis, enabled us to distinguish actively translating cells from negative controls, and to clearly quantify differences in translation activities in different strains and growth conditions. Specifically, we investigated K. phaffii at different growth rates, verified that methanol feeding alters translation activity, and analysed global translation in strains with genetically modified stress response pathways. Conclusions We set up a simple protocol to measure global translation activity in yeast on a single cell basis. The use of surfactants poses a practical and non-invasive alternative to the commonly used ergosterol pathway impaired strains and thus impacts a wide range of applications where increased drug and dye uptake is needed. |
topic |
Global translation activity Komagataella phaffii (Pichia pastoris) O-propargyl-puromycin (OPP) Surfactant Stress response |
url |
https://doi.org/10.1186/s12866-021-02185-3 |
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