Evidence map›Paper›PMID 6227627›Full record

ArticleThe Journal of cell biology1983

Interconversion of structural and contractile actin gels by insertion of myosin during assembly.

R E Kane

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1983. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. The role of the Arp2/3 complex in shaping the dynamics and structures of branched actomyosin networks.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  3. Forcing cells into shape: the mechanics of actomyosin contractility.Nature reviews. Molecular cell biology · 2015
    Review
  4. Article
  5. Active contractility in actomyosin networks.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Calcium-responsive contractility during fertilization in sea urchin eggs.Developmental dynamics : an official publication of the American Association of Anatomists · 2006
    Article
  11. Article
  12. Article
  13. Article
  14. Review
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

1 author.

R E Kane

Funding

CELL PROTEINS IN DIVISION AND EARLY DEVELOPMENTR01GM014363 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI KANE, ROBERT E · 1985 to 1985
–
NIGMS NIH HHS GM 14363
6 · The paper itself

Abstract

Extracts of the soluble cytoplasmic proteins of the sea urchin egg form gels of different composition and properties depending on the temperature used to induce actin polymerization. At temperatures that inactivate myosin, a gel composed of actin, fascin, and a 220,000-mol-wt protein is formed. Fascin binds actin into highly organized units with a characteristic banding pattern, and these actin-fascin units are the structural core of the sea urchin microvilli formed after fertilization and of the urchin coelomocyte filopods. Under milder conditions a more complex myosin-containing gel is formed, which contracts to a small fraction of its original volume within an hour after formation. What has been called "structural" gel can be assembled by combining actin, fascin, and the 220,000-mol-wt protein in 50-100 mM KCl; the aim of the experiments reported here was to determine whether myosin could be included during assembly, thereby interconverting structural and contractile gel. This approach is limited by the aggregation of sea urchin myosin at the low salt concentrations utilized in gel assembly. A method has been devised for the sequential combination of these components under controlled KCl and ATP concentrations that allows the formation of a gel containing dispersed myosin at a final concentration of 60-100 mM KCl. These gels are stable at low (approximately 10 micron) ATP concentrations, but contract to a small volume in the presence of higher (approximately 100 micron) ATP. Contraction can be controlled by forming a stable gel at low ATP and then overlaying it with a solution containing sufficient ATP to induce contraction. This system may provide a useful model for the study of the interrelations between cytoplasmic structure and motility.

Indexed as

ActinsAdenosine TriphosphatasesAnimalsElectrophoresis, Polyacrylamide GelFemaleFertilizationGelsKineticsMacromolecular SubstancesMaleMolecular WeightMusclesMyosinsOsmolar ConcentrationOvumSea UrchinsActinsAdenosine TriphosphatasesGelsMacromolecular SubstancesMyosins

Identifiers

PMID6227627
PMCPMC2112710
OpenAlexW2158769250

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.