Evidence map›Paper›PMID 35398095›Full record

ArticleThe Journal of biological chemistry2022

Mechanism of proteasome gate modulation by assembly chaperones Pba1 and Pba2.

Helena M Schnell, Jessie Ang, Shaun Rawson, Richard M Walsh, Yagmur Micoogullari, John Hanna

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

6 authors.

Helena M SchnellDepartment of Pathology, Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts, USA.
Jessie AngDepartment of Pathology, Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts, USA.
Shaun RawsonHarvard Cryo-Electron Microscopy Center for Structural Biology, Harvard Medical School, Boston, Massachusetts, USA; Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, Massachusetts, USA.
Richard M WalshHarvard Cryo-Electron Microscopy Center for Structural Biology, Harvard Medical School, Boston, Massachusetts, USA; Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, Massachusetts, USA.
Yagmur MicoogullariDepartment of Pathology, Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts, USA.
John HannaDepartment of Pathology, Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts, USA. Electronic address: jwhanna@bwh.harvard.edu.

Funding

New Ubiquitin-Proteasome System Components that Protect against ProteotoxicityDP5OD019800 · OD · BRIGHAM AND WOMEN'S HOSPITAL · PI HANNA, JOHN W · 2014 to 2018
$2.2M
Structural and Functional Analysis of Proteasome Core Particle BiogenesisR01GM144367 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI HANNA, JOHN W · 2022 to 2025
$1.6M
NIGMS NIH HHS R01 GM144367NIH HHS DP5 OD019800
6 · The paper itself

Abstract

The active sites of the proteasome are housed within its central core particle (CP), a barrel-shaped chamber of four stacked heptameric rings, and access of substrates to the CP interior is mediated by gates at either axial end. These gates are constitutively closed and may be opened by the regulatory particle (RP), which binds the CP and facilitates substrate degradation. We recently showed that the heterodimeric CP assembly chaperones Pba1/2 also mediate gate opening through an unexpected structural arrangement that facilitates the insertion of the N terminus of Pba1 into the CP interior; however, the full mechanism of Pba1/2-mediated gate opening is unclear. Here, we report a detailed analysis of CP gate modulation by Pba1/2. The clustering of key residues at the interface between neighboring α-subunits is a critical feature of RP-mediated gate opening, and we find that Pba1/2 recapitulate this strategy. Unlike RP, which inserts at six α-subunit interfaces, Pba1/2 insert at only two α-subunit interfaces. Nevertheless, Pba1/2 are able to regulate six of the seven interfacial clusters, largely through direct interactions. The N terminus of Pba1 also physically interacts with the center of the gate, disrupting the intersubunit contacts that maintain the closed state. This novel mechanism of gate modulation appears to be unique to Pba1/2 and therefore likely occurs only during proteasome assembly. Our data suggest that release of Pba1/2 at the conclusion of assembly is what allows the nascent CP to assume its mature gate conformation, which is primarily closed, until activated by RP.

Indexed as

Proteasome Endopeptidase ComplexSaccharomyces cerevisiae ProteinsCytoplasmMolecular ChaperonesSaccharomyces cerevisiaeMolecular ChaperonesPba1 protein, S cerevisiaePba2 protein, S cerevisiaeProteasome Endopeptidase ComplexSaccharomyces cerevisiae Proteinscore particlegateHbYXPba1Pba2proteasome

Identifiers

PMID35398095
PMCPMC9065996

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.