Evidence map›Paper›PMID 19242783›Full record

ArticleJournal of bioenergetics and biomembranes2009

The fully-active and structurally-stable form of the mitochondrial ATP synthase of Polytomella sp. is dimeric.

Alexa Villavicencio-Queijeiro, Miriam Vázquez-Acevedo, Araceli Cano-Estrada, Mariel Zarco-Zavala, Marietta Tuena de Gómez, Julio A Mignaco, Monica M Freire, Helena M Scofano, Debora Foguel, Pierre Cardol and 2 more

Abstract read
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In one paragraph

Article in Journal of bioenergetics and biomembranes, 2009. 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
0.9field-weighted citation impact, top 26% 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, 23 citations in OpenAlex.

  1. Article
  2. The Peripheral Stalk of Rotary ATPases.Frontiers in physiology · 2018
    Review
  3. Article
  4. 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

12 authors at 3 institutions in 3 countries.

Alexa Villavicencio-QueijeiroInstituto de Fisiología Celular, Universidad Nacional Autónoma de México, México DF, Mexico.
Miriam Vázquez-Acevedo
Araceli Cano-Estrada
Mariel Zarco-Zavala
Marietta Tuena de Gómez
Julio A Mignaco
Monica M Freire
Helena M Scofano
Debora Foguel
Pierre Cardol
Claire Remacle
Diego González-Halphen
Universidad Nacional Autónoma de México · MXUniversidade Federal do Rio de Janeiro · BRUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial F(1)F(O)-ATP synthase of chlorophycean algae is a stable dimeric complex of 1,600 kDa. It lacks the classic subunits that constitute the peripheral stator-stalk and the orthodox polypeptides involved in the dimerization of the complex. Instead, it contains nine polypeptides of unknown evolutionary origin named ASA1 to ASA9. The isolated enzyme exhibited a very low ATPase activity (0.03 Units/mg), that increased upon heat treatment, due to the release of the F(1) sector. Oligomycin was found to stabilize the dimeric structure of the enzyme, providing partial resistance to heat dissociation. Incubation in the presence of low concentrations of several non-ionic detergents increased the oligomycin-sensitive ATPase activity up to 7.0-9.0 Units/mg. Incubation with 3% (w/v) taurodeoxycholate monomerized the enzyme. The monomeric form of the enzyme exhibited diminished activity in the presence of detergents and diminished oligomycin sensitivity. Cross-linking experiments carried out with the dimeric and monomeric forms of the ATP synthase suggested the participation of the ASA6 subunit in the dimerization of the enzyme. The dimeric enzyme was more resistant to heat treatment, high hydrostatic pressures, and protease digestion than the monomeric enzyme, which was readily disrupted by these treatments. We conclude that the fully-active algal mitochondrial ATP synthase is a stable catalytically active dimer; the monomeric form is less active and less stable. Monomer-monomer interactions could be mediated by the membrane-bound subunits ASA6 and ASA9, and may be further stabilized by other polypeptides such as ASA1 and ASA5.

Indexed as

Protein ConformationChlorophytaDimerizationElectrophoresis, Polyacrylamide GelMitochondrial Proton-Translocating ATPasesProtein SubunitsMitochondrial Proton-Translocating ATPasesProtein Subunits

Identifiers

PMID19242783
OpenAlexW2054531333

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.