Evidence map›Paper›PMID 38635626›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

A chemical inhibitor of IST1-CHMP1B interaction impairs endosomal recycling and induces noncanonical LC3 lipidation.

Anastasia Knyazeva, Shuang Li, Dale P Corkery, Kasturika Shankar, Laura K Herzog, Xuepei Zhang, Birendra Singh, Georg Niggemeyer, David Grill, Jonathan D Gilthorpe and 4 more

RetractedErratum issuedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Exosomal-complement system activation in preeclampsia.The journal of obstetrics and gynaecology research · 2025
    Review
  10. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Anastasia Knyazeva *Department of Chemistry, Umeå University, 901 87 Umeå, Sweden.
Shuang Li *Department of Chemistry, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0001-7708-0166
Dale P CorkeryDepartment of Chemistry, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0001-7930-0134
Kasturika ShankarUmeå Centre for Microbial Research, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0002-0011-3756
Laura K HerzogDepartment of Chemistry, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0002-3322-7864
Xuepei ZhangChemical Proteomics Core Facility, Division of Chemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, 171 77 Stockholm, Sweden.
Birendra SinghDepartment of Surgical and Perioperative Sciences, Unit of Anesthesiology and Intensive Care Medicine, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0002-7246-1442
Georg NiggemeyerDepartment of Chemical Biology, Max Planck Institute of Molecular Physiology, 44227, Dortmund, Germany.
David GrillDepartment of Chemical Biology, Max Planck Institute of Molecular Physiology, 44227, Dortmund, Germany.
Jonathan D GilthorpeDepartment of Integrative Medical Biology, Umeå University, 901 87, Umeå, Sweden.ORCID 0000-0002-6884-4774
Massimiliano GaetaniChemical Proteomics Core Facility, Division of Chemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, 171 77 Stockholm, Sweden.ORCID 0000-0001-5610-0797
Lars-Anders CarlsonUmeå Centre for Microbial Research, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0003-2342-6488
Herbert WaldmannDepartment of Chemical Biology, Max Planck Institute of Molecular Physiology, 44227, Dortmund, Germany.ORCID 0000-0002-9606-7247
Yao-Wen WuDepartment of Chemistry, Umeå University, 901 87 Umeå, Sweden.ORCID 0000-0002-2573-8736
Science for Life Laboratory · SEUmeå University · SEMax Planck Institute of Molecular Physiology · DETU Dortmund University · DE

Funding

EC | European Research Council (ERC) ChemBioAPGoran Gustafsson Foundation for Research in Natural Sciences and Medicine GG prizeKnut och Alice Wallenbergs Stiftelse (Knut and Alice Wallenberg Foundation) WAF2016Vetenskapsrådet (VR) 2018-04585 2022-02932
6 · The paper itself

Abstract

The endosomal sorting complex required for transport (ESCRT) machinery constitutes multisubunit protein complexes that play an essential role in membrane remodeling and trafficking. ESCRTs regulate a wide array of cellular processes, including cytokinetic abscission, cargo sorting into multivesicular bodies (MVBs), membrane repair, and autophagy. Given the versatile functionality of ESCRTs, and the intricate organizational structure of the ESCRT machinery, the targeted modulation of distinct ESCRT complexes is considerably challenging. This study presents a pseudonatural product targeting IST1-CHMP1B within the ESCRT-III complexes. The compound specifically disrupts the interaction between IST1 and CHMP1B, thereby inhibiting the formation of IST1-CHMP1B copolymers essential for normal-topology membrane scission events. While the compound has no impact on cytokinesis, MVB sorting, or biogenesis of extracellular vesicles, it rapidly inhibits transferrin receptor recycling in cells, resulting in the accumulation of transferrin in stalled sorting endosomes. Stalled endosomes become decorated by lipidated LC3, suggesting a link between noncanonical LC3 lipidation and inhibition of the IST1-CHMP1B complex.

Indexed as

Endosomal Sorting Complexes Required for TransportEndosomesMultivesicular BodiesProtein TransportEndosomal Sorting Complexes Required for Transportendosomal recyclingESCRTIST1-CHMP1Bnoncanonical LC3 lipidationTantalosin

Identifiers

PMID38635626
PMCPMC11047075
OpenAlexW4394933370

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.