Evidence map›Paper›PMID 34772928›Full record

ArticleNature communications2021

An integrative proteomics method identifies a regulator of translation during stem cell maintenance and differentiation.

Pierre Sabatier, Christian M Beusch, Amir A Saei, Mike Aoun, Noah Moruzzi, Ana Coelho, Niels Leijten, Magnus Nordenskjöld, Patrick Micke, Diana Maltseva and 13 more

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

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  15. Stability-based approaches in chemoproteomics.Expert reviews in molecular medicine · 2024
    Review
  16. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Pierre SabatierChemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.ORCID 0000-0002-2734-1791
Christian M BeuschChemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.ORCID 0000-0001-9100-8283
Amir A SaeiChemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.ORCID 0000-0002-2639-6328
Mike AounDivision of Medical Inflammation Research, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.
Noah MoruzziThe Rolf Luft Research Center for Diabetes and Endocrinology, Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, 17176, Sweden.
Ana CoelhoDivision of Medical Inflammation Research, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.
Niels LeijtenBiomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Padualaan 8, Utrecht, 3584 CH, The Netherlands.ORCID 0000-0002-7305-7249
Magnus NordenskjöldCenter for Molecular Medicine, Karolinska University Hospital, Stockholm, 171 76, Sweden.
Patrick MickeImmunology, Genetics and Pathology, Rudbecklaboratoriet, Uppsala University, Uppsala, 751 85, Sweden.ORCID 0000-0003-1210-5961
Diana MaltsevaFaculty of biology and biotechnology, National Research University Higher School of Economics, Myasnitskaya Street, 13/4, Moscow, 117997, Russia.ORCID 0000-0002-4960-5348
Alexander G TonevitskyFaculty of biology and biotechnology, National Research University Higher School of Economics, Myasnitskaya Street, 13/4, Moscow, 117997, Russia.
Vincent MillischerDepartment of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, 17177, Sweden.
J Carlos VillaescusaNeurogenetic Unit, Department of Molecular Medicine and Surgery, Karolinska University Hospital, Stockholm, 171 76, Sweden.
Sandeep KadekarDepartment of Surgical Sciences, Uppsala University, Uppsala, 752 37, Sweden.
Massimiliano GaetaniChemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.ORCID 0000-0001-5610-0797
Kamilya AltynbekovageneXplain GmbH, Am Exer 19B, 38302, Wolfenbuettel, Germany.
Alexander KelgeneXplain GmbH, Am Exer 19B, 38302, Wolfenbuettel, Germany.
Per-Olof BerggrenThe Rolf Luft Research Center for Diabetes and Endocrinology, Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, 17176, Sweden.
Oscar SimonsonDepartment of Surgical Sciences, Uppsala University, Uppsala, 752 37, Sweden.
Karl-Henrik GrinnemoDepartment of Surgical Sciences, Uppsala University, Uppsala, 752 37, Sweden.
Rikard HolmdahlDivision of Medical Inflammation Research, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden.ORCID 0000-0002-4969-2576
Sergey RodinChemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden. sergey.rodin@surgsci.uu.se.ORCID 0000-0002-6954-1986
Roman A ZubarevChemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, 17177, Sweden. roman.zubarev@ki.se.ORCID 0000-0001-9839-2089

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detailed characterization of cell type transitions is essential for cell biology in general and particularly for the development of stem cell-based therapies in regenerative medicine. To systematically study such transitions, we introduce a method that simultaneously measures protein expression and thermal stability changes in cells and provide the web-based visualization tool ProteoTracker. We apply our method to study differences between human pluripotent stem cells and several cell types including their parental cell line and differentiated progeny. We detect alterations of protein properties in numerous cellular pathways and components including ribosome biogenesis and demonstrate that modulation of ribosome maturation through SBDS protein can be helpful for manipulating cell stemness in vitro. Using our integrative proteomics approach and the web-based tool, we uncover a molecular basis for the uncoupling of robust transcription from parsimonious translation in stem cells and propose a method for maintaining pluripotency in vitro.

Indexed as

Cell DifferentiationCell LineHumansPluripotent Stem CellsProteomics

Identifiers

PMID34772928
PMCPMC8590018

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.