Evidence map›Paper›PMID 1906474›Full record

ArticleThe Journal of cell biology1991

Synapsin I-mediated interaction of brain spectrin with synaptic vesicles.

A F Sikorski, G Terlecki, I S Zagon, S R Goodman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 88 citations in OpenAlex.

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  10. Tissue-type plasminogen activator triggers the synaptic vesicle cycle in cerebral cortical neurons.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2015
    Article
  11. Genome-wide association study of neocortical Lewy-related pathology.Annals of clinical and translational neurology · 2015
    Article
  12. Spectrin's chimeric E2/E3 enzymatic activity.Experimental biology and medicine (Maywood, N.J.) · 2015
    Review
  13. Article
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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

4 authors at 1 institution in 2 countries.

A F SikorskiDepartment of Structural and Cellular Biology, College of Medicine, University of South Alabama, Mobile 36688.
G Terlecki
I S Zagon
S R Goodman
Pennsylvania State University · US

Funding

SPECTRIN-LIKE PROTEIN IN BRAINR01NS019357 · NINDS · UNIVERSITY OF SOUTH ALABAMA · PI GOODMAN, STEVEN RICHARD · 1985 to 1994
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STRUCTURE, LOCATION AND FUNCTION OF BRAIN AMELINR01NS026536 · NINDS · UNIVERSITY OF SOUTH ALABAMA · PI GOODMAN, STEVEN RICHARD · 1988 to 1992
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NINDS NIH HHS NS-19357NINDS NIH HHS NS-26536
6 · The paper itself

Abstract

We have established a new binding assay in which 125I-labeled synaptic vesicles are incubated with brain spectrin covalently immobilized on cellulosic membranes in a microfiltration apparatus. We obtained saturable, high affinity, salt- (optimum at 50-70 mM NaCl) and pH- (optimum at pH 7.5-7.8) dependent binding. Nonlinear regression analysis of the binding isotherm indicated one site binding with a Kd = 59 micrograms/ml and a maximal binding capacity = 1.9 micrograms vesicle protein per microgram spectrin. The fact that the binding of spectrin was via synapsin was demonstrated in three ways. (a) Binding of synaptic vesicles to immobilized spectrin was eliminated by prior extraction with 1 M KCl. When the peripheral membrane proteins in the 1 M KCl extract were separated by SDS-PAGE, transferred to nitrocellulose paper and incubated with 125I-brain spectrin, 96% of the total radioactivity was associated with five polypeptides of 80, 75, 69, 64, and 40 kD. All five polypeptides reacted with an anti-synapsin I polyclonal antibody, and the 80- and 75-kD polypeptides comigrated with authentic synapsin Ia and synapsin Ib. The 69- and 64-kD polypeptides are either proteolytic fragments of synapsin I or represent synapsin IIa and synapsin IIb. (b) Pure synapsin I was capable of competitively inhibiting the binding of radioiodinated synaptic vesicles to immobilized brain spectrin with a Kl = 46 nM. (c) Fab fragments of anti-synapsin I were capable of inhibiting the binding of radioiodinated synaptic vesicles to immobilized brain spectrin. These three observations clearly establish that synapsin I is a primary receptor for brain spectrin on the cytoplasmic surface of the synaptic vesicle membrane.

Indexed as

AnimalsBlotting, WesternBrainBrain ChemistryCattleElectrophoresis, Polyacrylamide GelIntracellular MembranesNerve Tissue ProteinsProtein BindingRegression AnalysisSpectrinSynapsinsSynaptic VesiclesNerve Tissue ProteinsSpectrinSynapsins

Identifiers

PMID1906474
PMCPMC2289068
OpenAlexW2000735919

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.