Evidence map›Paper›PMID 22451649›Full record

ArticleThe Journal of biological chemistry2012

The role of ERp44 in maturation of serotonin transporter protein.

Samuel Freyaldenhoven, Yicong Li, Arif M Kocabas, Enrit Ziu, Serra Ucer, Raman Ramanagoudr-Bhojappa, Grover P Miller, Fusun Kilic

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in The Journal of biological chemistry, 2012. 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 It has been retracted, and should not be counted.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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. GDM-associated insulin deficiency hinders the dissociation of SERT from ERp44 and down-regulates placental 5-HT uptake.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Trial
  3. Article
  4. Article
  5. Frontiers of Serotonin Beyond the Brain.Pharmacological research · 2019
    Article
  6. Article
  7. Structural basis of pH-dependent client binding by ERp44, a key regulator of protein secretion at the ER-Golgi interface.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  8. Article
  9. Article
  10. Ero1-PDI interactions, the response to redox flux and the implications for disulfide bond formation in the mammalian endoplasmic reticulum.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2013
    Article
  11. Missing links in antibody assembly control.International journal of cell biology · 2013
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Samuel FreyaldenhovenDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Yicong LiDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Arif M KocabasDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Enrit ZiuDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Serra UcerDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Raman Ramanagoudr-BhojappaDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Grover P MillerDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205.
Fusun KilicDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205. Electronic address: kilicfusun@uams.edu.
University of Arkansas for Medical Sciences · US

Funding

Communication between platelet SERT and plasma 5HTR01HL091196 · NHLBI · UNIV OF ARKANSAS FOR MED SCIS · PI KILIC, FUSUN · 2009 to 2014
$2.2M
Placental serotonin transporter uses ERp44 and Ero1-L for maturation.R03HD058697 · NICHD · UNIV OF ARKANSAS FOR MED SCIS · PI KILIC, FUSUN · 2009 to 2010
$143k
Impact of Diabetes on Placental Serotonin TransporterR03HD053477 · NICHD · UNIV OF ARKANSAS FOR MED SCIS · PI KILIC, FUSUN · 2006 to 2007
$140k
NHLBI NIH HHS HL091196NHLBI NIH HHS HL091196-01A2W1NHLBI NIH HHS R01 HL091196NICHD NIH HHS HD053477NICHD NIH HHS HD058697NICHD NIH HHS R03 HD053477NICHD NIH HHS R03 HD058697
6 · The paper itself

Abstract

In heterologous and endogenous expression systems, we studied the role of ERp44 and its complex partner endoplasmic reticulum (ER) oxidase 1-α (Ero1-Lα) in mechanisms regulating disulfide bond formation for serotonin transporter (SERT), an oligomeric glycoprotein. ERp44 is an ER lumenal chaperone protein that favors the maturation of disulfide-linked oligomeric proteins. ERp44 plays a critical role in the release of proteins from the ER via binding to Ero1-Lα. Mutation in the thioredoxin-like domain hampers the association of ERp44C29S with SERT, which has three Cys residues (Cys-200, Cys-209, and Cys-109) on the second external loop. We further explored the role of the protein chaperones through shRNA knockdown experiments for ERp44 and Ero1-Lα. Those efforts resulted in increased SERT localization to the plasma membrane but decreased serotonin (5-HT) uptake rates, indicating the importance of the ERp44 retention mechanism in the proper maturation of SERT proteins. These data were strongly supported with the data received from the N-biotinylaminoethyl methanethiosulfonate (MTSEA-biotin) labeling of SERT on ERp44 shRNA cells. MTSEA-biotin only interacts with the free Cys residues from the external phase of the plasma membrane. Interestingly, it appears that Cys-200 and Cys-209 of SERT in ERp44-silenced cells are accessible to labeling by MTSEA-biotin. However, in the control cells, these Cys residues are occupied and produced less labeling with MTSEA-biotin. Furthermore, ERp44 preferentially associated with SERT mutants (C200S, C209S, and C109A) when compared with wild type. These interactions with the chaperone may reflect the inability of Cys-200 and Cys-209 SERT mutants to form a disulfide bond and self-association as evidenced by immunoprecipitation assays. Based on these collective findings, we hypothesize that ERp44 together with Ero1-Lα plays an important role in disulfide formation of SERT, which may be a prerequisite step for the assembly of SERT molecules in oligomeric form.

Indexed as

Cell LineCell MembraneDisulfidesFemaleGene SilencingHumansMembrane GlycoproteinsMembrane ProteinsMolecular ChaperonesMutationOxidoreductasesProtein MultimerizationProtein Structure, TertiarySerotonin Plasma Membrane Transport ProteinsDisulfidesERO1A protein, humanERP44 protein, humanMembrane GlycoproteinsMembrane ProteinsMolecular ChaperonesOxidoreductasesSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID22451649
PMCPMC3366855
OpenAlexW2062840903

What OpenQuestion 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 OpenQuestion graph.