JacksonLab @CBJacksonLab
Studying cellular signalling and proteostasis in response to mitochondrial dysfunction. jacksonlab.org Helsinki, Finland Joined June 2019-
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🔥This opens a path toward targeting v-ATPase with precision, with implications from cancer to mitochondrial disease.
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Mild v-ATPase inhibition boosts ΔΨm and restores cell fitness under mitochondrial mistranslation stress — even in patient-derived fibroblasts. 🔬A major effort led by Geoffray, revealing how cells deploy extra-organellar control to survive mitochondrial dysfunction.
🚨 New from our lab (est. 2020) — now published in Nature Communications! 🧬We uncover a surprising link between the v-ATPaseand mitochondrial function: Mild v-ATPase inhibition restores cell fitness under mitochondrial mistranslation stress nature.com/articles/s4146… (Thread ⬇️)
JacksonLab retweeted
Together with @mito_oncogene, today we report in Nature Genetics a peculiar + exciting discovery: positive selection of mutations to mitochondrial ribosomal RNA in cancer. Led by Sonia Boscenco, Jacqueline Tait-Mulder, and Minsoo Kim nature.com/articles/s4158…
JacksonLab retweeted
Local de novo synthesis of serine delays mitochondrial muscle disease progression. Tour de force work of Christopher Jackson and @marmyleva_ana Anastasiia Marmyleva. Congrats Anastasiia especially for your first 1st author paper! @ASW_lab cell.com/cell-reports/f…
JacksonLab retweeted
✨Excited to share our new paper in @CellReports! ✨We show how cells rely on self-made serine to protect themselves under mitochondrial stress. Huge thanks to my mentors @CBJacksonLab and @AWartiovaara 🙏 cell.com/cell-reports/f…
JacksonLab retweeted
Unique architectural features of mammalian mitochondrial protein synthesis 30-day free access to our new review at: authors.elsevier.com/a/1jE3u3QxxSux… Thanks to all the authors for their insightful contributions and our editor for their kind invitation and guidance.
JacksonLab retweeted
Please check out out our paper with @CBJacksonLab and @Solocanuck👇 Supernumerary proteins of the human mitochondrial ribosomal small subunit are integral for assembly and translation cell.com/iscience/fullt… @GMonteuuis @KrysiaBroda @ElizabethPyman @_DiegoBalboa_ 1/7
JacksonLab retweeted
In the latest issue! Problem choice and decision trees in science and engineering dlvr.it/T5V7S5
JacksonLab retweeted
Our mapping of the cellular protein #interactome with unprecedented depth is now published @Nature. Leaps in robust #proteomics and analytic workflows enabled us to perform over 4.000 pull-downs in yeast unraveling the social and structural aspects leveraging #alphafold multimer.
Protein interactions are the foundation of functional and healthy cells. We @labs_mann are proud that our work for mapping the cellular yeast #interactome on a global scale is now published @nature. nature.com/articles/s4158… yeast-interactome.org #proteomics #massspectrometry
JacksonLab retweeted
Welcome to the Metabolism seminar on Friday, Oct 13th at 9-11 am, Haartman Institute Lecture Hall 2. Talks on nutrient transporters in cancer and mitochondrial quality control by @Rafabolism and @CBJacksonLab ☕️🍪at 8:30. Spread the word @STEMMProgram @HelsinkiUniMed @BIOTECH_UH
World Mitochondrial Disease Week mitochondrialdiseaseweek.org
in other words: 700 Million people worth of cells.
“… it is estimated, 50m tonnes of her cells have been produced.”
@coffee_lipe Beware of age-induced astigmatism.
JacksonLab retweeted
Our preprint show that knock-in mice with drastically reduced levels respirasomes have normal OXPHOS function and no obvious phenotypes! Very unexpected results indeed! Presented the story at EuroMit. Thanks all coauthors for a very nice collaboration! biorxiv.org/content/10.110…
JacksonLab retweeted
TransitID is out today in Cell! This is a proximity labeling method for unbiased discovery of endogenous proteins that traffick from a defined “source” location to a defined “destination” location. TransitID uses sequential labeling by TurboID in the source, followed by a chase period (minutes to hours) and then 1-minute APEX tagging in the destination compartment. Proteins tagged by both enzymes are enriched with streptavidin and anti-fluorescein antibody, and identified by mass spec. We explore 4 intracellular and intercellular applications of TransitID: - discovery of locally translated mitochondrial proteins (translated at OMM, then imported into mito matrix) - mapping proteins whose cytoplasm-to-nucleus shuttling is dampened by stress - discovery of proteins that transit between nucleolus & stress granules during stress & stress recovery - analysis of proteins that traffic intercellularly bw tumor cells & macrophages Work of amazingly talented co-first authors @WeiQinChemBio and @CheahJoleen, and collaborators Steve Carr @namude & Paul Taylor authors.elsevier.com/a/1hKLcL7PXmcqA
Interested in a postdoctoral project encompassing genome-wide CRISPR/Cas9 screening and mitochondrial metabolism? Let’s apply for a Marie Sklodowska-Curie Postdoctoral Fellowship. Deadline: 13.09.2023 #msca #postdoc #fellowship #funding
PhD position available in our group: project in genome-wide signalling and cell-type-specific susceptibility to mitochondrial translation defects. Please RT and get in touch jacksonlab.org @mitojobs
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