Evidence map›Paper›PMID 32997735›Full record

ArticleThe Journal of cell biology2020

Combinatorial multivalent interactions drive cooperative assembly of the COPII coat.

Viktoriya G Stancheva, Xiao-Han Li, Joshua Hutchings, Natalia Gomez-Navarro, Balaji Santhanam, M Madan Babu, Giulia Zanetti, Elizabeth A Miller

Abstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Review
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  6. SHARK enables sensitive detection of evolutionary homologs and functional analogs in unalignable and disordered sequences.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. ULK/Atg1: phasing in and out of autophagy.Trends in biochemical sciences · 2024
    Review
  9. Article
  10. ER exit in physiology and disease.Frontiers in molecular biosciences · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. An in vitro vesicle formation assay reveals cargo clients and factors that mediate vesicular trafficking.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. Article
  20. Article
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

8 authors.

Viktoriya G StanchevaMRC Laboratory of Molecular Biology, Cambridge, UK.
Xiao-Han LiMRC Laboratory of Molecular Biology, Cambridge, UK.
Joshua HutchingsInstitute of Structural and Molecular Biology, Birkbeck College, London, UK.
Natalia Gomez-NavarroMRC Laboratory of Molecular Biology, Cambridge, UK.
Balaji SanthanamMRC Laboratory of Molecular Biology, Cambridge, UK.
M Madan BabuMRC Laboratory of Molecular Biology, Cambridge, UK.
Giulia ZanettiInstitute of Structural and Molecular Biology, Birkbeck College, London, UK.
Elizabeth A MillerMRC Laboratory of Molecular Biology, Cambridge, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/T002670/1Medical Research Council MC_U105185859Medical Research Council MC_UP_1201/10
6 · The paper itself

Abstract

Protein secretion is initiated at the endoplasmic reticulum by the COPII coat, which self-assembles to form vesicles. Here, we examine the mechanisms by which a cargo-bound inner coat layer recruits and is organized by an outer scaffolding layer to drive local assembly of a stable structure rigid enough to enforce membrane curvature. An intrinsically disordered region in the outer coat protein, Sec31, drives binding with an inner coat layer via multiple distinct interfaces, including a newly defined charge-based interaction. These interfaces combinatorially reinforce each other, suggesting coat oligomerization is driven by the cumulative effects of multivalent interactions. The Sec31 disordered region could be replaced by evolutionarily distant sequences, suggesting plasticity in the binding interfaces. Such a multimodal assembly platform provides an explanation for how cells build a powerful yet transient scaffold to direct vesicle traffic.

Indexed as

COP-Coated VesiclesEndoplasmic ReticulumGTPase-Activating ProteinsProtein BindingProtein TransportSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsVesicular Transport ProteinsGTPase-Activating ProteinsSaccharomyces cerevisiae ProteinsSEC23 protein, S cerevisiaeVesicular Transport Proteins

Identifiers

PMID32997735
PMCPMC7594496

What OpenQuestion holds

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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 OpenQuestion graph.