Evidence map›Paper›PMID 21381722›Full record

ArticleBiochemistry2011

Mitsugumin 23 forms a massive bowl-shaped assembly and cation-conducting channel.

Elisa Venturi, Kazuhiro Mio, Miyuki Nishi, Toshihiko Ogura, Toshio Moriya, Samantha J Pitt, Kazutaka Okuda, Sho Kakizawa, Rebecca Sitsapesan, Chikara Sato and 1 more

Abstract read
In one paragraph

Article in Biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The ion channels of endomembranes.Physiological reviews · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Dysregulated ZnThe Journal of biological chemistry · 2017
    Article
  11. Review
  12. 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

11 authors at 4 institutions in 2 countries.

Elisa VenturiSchool of Physiology and Pharmacology, Bristol Heart Institute and Centre for Nanoscience and Quantum Information, University of Bristol, Bristol, United Kingdom.
Kazuhiro Mio
Miyuki Nishi
Toshihiko Ogura
Toshio Moriya
Samantha J Pitt
Kazutaka Okuda
Sho Kakizawa
Rebecca Sitsapesan
Chikara Sato
Hiroshi Takeshima
National Institute of Advanced Industrial Science and Technology · JPUniversity of Bristol · GBKyoto Pharmaceutical University · JPKyoto University · JP

Funding

British Heart Foundation
6 · The paper itself

Abstract

Mitsugumin 23 (MG23) is a 23 kDa transmembrane protein localized to the sarcoplasmic/endoplasmic reticulum and nuclear membranes in a wide variety of cells. Although the characteristics imply the participation in a fundamental function in intracellular membrane systems, the physiological role of MG23 is unknown. Here we report the biochemical and biophysical characterization of MG23. Hydropathicity profile and limited proteolytic analysis proposed three transmembrane segments in the MG23 primary structure. Chemical cross-linking analysis suggested a homo-oligomeric assembly of MG23. Ultrastructural observations detected a large symmetrical particle as the predominant component and a small asymmetric assembly as the second major component in highly purified MG23 preparations. Single-particle three-dimensional reconstruction revealed that MG23 forms a large bowl-shaped complex equipped with a putative central pore, which is considered an assembly of the small asymmetric subunit. After reconstitution into planar phospholipid bilayers, purified MG23 behaved as a voltage-dependent, cation-conducting channel, permeable to both K(+) and Ca(2+). A feature of MG23 gating was that multiple channels always appeared to be gating together in the bilayer. Our observations suggest that the bowl-shaped MG23 can transiently assemble and disassemble. These building transitions may underlie the unusual channel gating behavior of MG23 and allow rapid cationic flux across intracellular membrane systems.

Indexed as

AnimalsCalciumCross-Linking ReagentsEndoplasmic ReticulumHumansHydrophobic and Hydrophilic InteractionsImaging, Three-DimensionalIon ChannelsLipid BilayersMembrane ProteinsMicroscopy, ElectronPeptide FragmentsPotassiumProtein ConformationProtein SubunitsRabbitsCalciumCross-Linking ReagentsIon ChannelsLipid BilayersMembrane Proteinsmitsugumin23 protein, humanPeptide FragmentsPotassiumProtein SubunitsRecombinant Proteins

Identifiers

PMID21381722
PMCPMC3065873
OpenAlexW2043330139

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.