Evidence map›Paper›PMID 30910017›Full record

ArticleMethods in enzymology2019

Assays for protein retrotranslocation in ERAD.

Sonya Neal, Sascha H Duttke, Randolph Y Hampton

Open access · greenAbstract read
In one paragraph

Article in Methods in enzymology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Assays for studying normalSTAR protocols · 2021
    Article
  5. 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

3 authors at 1 institution in 1 country.

Sonya NealDivision of Biological Sciences, The Section of Cell and Developmental Biology, University of California San Diego, La Jolla, CA, United States. Electronic address: seneal@ucsd.edu.
Sascha H DuttkeDepartment of Medicine, University of California San Diego, La Jolla, CA, United States.
Randolph Y HamptonDivision of Biological Sciences, The Section of Cell and Developmental Biology, University of California San Diego, La Jolla, CA, United States.
University of California, San Diego · US

Funding

Protein degradation and cholesterol regulationR37DK051996 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMPTON, RANDOLPH Y. · 2012 to 2020
$3.2M
The Discovery of Molecules and Mechanisms of the Rhomboid SuperfamilyR35GM133565 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Sonya Elina Neal · 2019 to 2026
$2.9M
Discovering the machinery and mechanism of ERAD-M retrotranslocationF32GM111024 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NEAL, SONYA ELINA · 2014 to 2016
$164k
NIDDK NIH HHS R37 DK051996NIGMS NIH HHS F32 GM111024NIGMS NIH HHS R35 GM133565
6 · The paper itself

Abstract

Elimination of misfolded proteins by endoplasmic reticulum (ER)-associated protein degradation (ERAD) ensures that proteins proceeding through the secretory pathway are correctly folded and processed, which is critical to minimize ER stress. All ERAD pathways include a protein translocation process termed retrotranslocation, in which ubiquitinated misfolded substrates are extracted from the ER and degraded by the cytosolic 26S proteasome. Despite being integral to ERAD, the retrotranslocation process has been largely obscure. Recently, an explosion of discoveries has provided key mechanistic insights into this novel route of protein transport. These advances were facilitated by the development of in vitro and in vivo assays that utilize components from the yeast Saccharomyces cerevisiae. The assays permit detailed study of the distinct steps in ERAD-linked retrotranslocation, including ubiquitination of selected ERAD substrates, substrate removal from the ER, maintenance of cytosolic substrate solubility in the cytosol, and substrate degradation. Here we provide detailed protocols for these assays that pertain to work on retrotranslocation of integral membrane proteins (ERAD-M substrates), with the expectation that these approaches can be adapted for many related biochemical processes.

Indexed as

Endoplasmic Reticulum-Associated DegradationProteasome Endopeptidase ComplexProtein FoldingProtein TransportProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsUbiquitinationProteasome Endopeptidase ComplexSaccharomyces cerevisiae ProteinsCdc48Dfm1Doa10ERERADHmg2Hrd1RetrochaperoneRetrotranslocation

Identifiers

PMID30910017
PMCPMC10802991
OpenAlexW2912750849

What OpenQuestion holds

Textmetadata
LicenceTDM
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.