Summary of Study ST002478

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001601. The data can be accessed directly via it's Project DOI: 10.21228/M8RH99 This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002478
Study TitleThe effect of prions on cellular metabolism: The metabolic impact of the [RNQ+] prion and the native role of Rnq1p
Study SummaryWithin the field of amyloid and prion disease there is a need for a more comprehensive understanding of the fundamentals of disease biology. In order to facilitate the progression treatment and underpin comprehension of toxicity, fundamental understanding of the disruption to normal cellular biochemistry and trafficking is needed. Here, by removing the complex biochemistry of the brain, we have utilised known prion forming strains of Saccharomyces cerevisiae carrying different conformational variants of the Rnq1p to obtain Liquid Chromatography-Mass Spectrometry (LC-MS) metabolic profiles and identify key perturbations of prion presence. These studies reveal that prion containing [RNQ+] cells display a significant reduction in amino acid biosynthesis and distinct perturbations in sphingolipid metabolism, with significant downregulation in metabolites within these pathways. Moreover, that native Rnq1p downregulates ubiquinone biosynthesis pathways within cells, suggesting that Rnq1p may play a lipid/mevalonate-based cytoprotective role as a regulator of ubiquinone production. These findings contribute to the understanding of how prion proteins interact in vivo in both their prion and non-prion confirmations and indicate potential targets for the mitigation of these effects. . We demonstrate specific sphingolipid centred metabolic disruptions due to prion presence and give insight into a potential cytoprotective role of the native Rnq1 protein. This provides evidence of metabolic similarities between yeast and mammalian cells as a consequence of prion presence and establishes the application of metabolomics as a tool to investigate prion/amyloid-based phenomena.
Institute
Canterbury Christ Church University
Last NameHowell-Bray
First NameTyler
Address46 Canterbury Road, Kent
Emailt.l.howellbray@gmail.com
Phone07841631495
Submit Date2022-10-12
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2023-02-26
Release Version1
Tyler Howell-Bray Tyler Howell-Bray
https://dx.doi.org/10.21228/M8RH99
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Yeast; Subject species: Saccharomyces cerevisiae (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA248069rnq-StressPIM50.2mM H202 | Ion mode:negative
SA248070rnq-StressPIM60.2mM H202 | Ion mode:negative
SA248071rnq-StressPIM40.2mM H202 | Ion mode:negative
SA248072rnq-StressNIM30.2mM H202 | Ion mode:negative
SA248073rnq-StressNIM60.2mM H202 | Ion mode:negative
SA248074rnq-StressNIM20.2mM H202 | Ion mode:negative
SA248075rnq-StressNIM10.2mM H202 | Ion mode:negative
SA248076rnq-StressPIM20.2mM H202 | Ion mode:negative
SA248077rnq-StressPIM10.2mM H202 | Ion mode:negative
SA248078rnq-StressNIM50.2mM H202 | Ion mode:negative
SA248079rnq-StressNIM40.2mM H202 | Ion mode:negative
SA248080rnq-StressPIM30.2mM H202 | Ion mode:negative
SA248057RNQ+StressNIM30.2mM H202 | Ion mode:Positive
SA248058RNQ+StressNIM40.2mM H202 | Ion mode:Positive
SA248059RNQ+StressNIM20.2mM H202 | Ion mode:Positive
SA248060RNQ+StressNIM10.2mM H202 | Ion mode:Positive
SA248061RNQ+StressNIM60.2mM H202 | Ion mode:Positive
SA248062RNQ+StressNIM50.2mM H202 | Ion mode:Positive
SA248063RNQ+StressPIM10.2mM H202 | Ion mode:Positive
SA248064RNQ+StressPIM60.2mM H202 | Ion mode:Positive
SA248065RNQ+StressPIM50.2mM H202 | Ion mode:Positive
SA248066RNQ+StressPIM40.2mM H202 | Ion mode:Positive
SA248067RNQ+StressPIM30.2mM H202 | Ion mode:Positive
SA248068RNQ+StressPIM20.2mM H202 | Ion mode:Positive
SA248093rnq-PIM6none | Ion mode:negative
SA248094rnq-PIM5none | Ion mode:negative
SA248095DeltaPIM1none | Ion mode:negative
SA248096rnq-NIM1none | Ion mode:negative
SA248097rnq-NIM2none | Ion mode:negative
SA248098rnq-NIM3none | Ion mode:negative
SA248099rnq-NIM4none | Ion mode:negative
SA248100DeltaNIM6none | Ion mode:negative
SA248101DeltaNIM5none | Ion mode:negative
SA248102DeltaNIM2none | Ion mode:negative
SA248103DeltaNIM3none | Ion mode:negative
SA248104DeltaNIM4none | Ion mode:negative
SA248105rnq-NIM5none | Ion mode:negative
SA248106DeltaNIM1none | Ion mode:negative
SA248107rnq-PIM1none | Ion mode:negative
SA248108rnq-PIM2none | Ion mode:negative
SA248109rnq-PIM3none | Ion mode:negative
SA248110DeltaPIM6none | Ion mode:negative
SA248111DeltaPIM5none | Ion mode:negative
SA248112DeltaPIM2none | Ion mode:negative
SA248113DeltaPIM3none | Ion mode:negative
SA248114DeltaPIM4none | Ion mode:negative
SA248115rnq-PIM4none | Ion mode:negative
SA248081RNQ+PIM3none | Ion mode:Positive
SA248082RNQ+PIM1none | Ion mode:Positive
SA248083RNQ+PIM2none | Ion mode:Positive
SA248084RNQ+NIM3none | Ion mode:Positive
SA248085RNQ+PIM4none | Ion mode:Positive
SA248086RNQ+PIM5none | Ion mode:Positive
SA248087RNQ+PIM6none | Ion mode:Positive
SA248088RNQ+NIM1none | Ion mode:Positive
SA248089RNQ+NIM2none | Ion mode:Positive
SA248090RNQ+NIM5none | Ion mode:Positive
SA248091RNQ+NIM6none | Ion mode:Positive
SA248092RNQ+NIM4none | Ion mode:Positive
Showing results 1 to 59 of 59
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