Evidence map›Paper›PMID 23862673›Full record

ArticleBiochemistry2013

Assembly of high molecular weight complexes of lipin on a supported lipid bilayer observed by atomic force microscopy.

Carl E Creutz, James M Eaton, Thurl E Harris

Erratum issuedAbstract read
In one paragraph

Article in Biochemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 34% 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, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Carl E CreutzDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia 22908, United States. creutz@virginia.edu
James M Eaton
Thurl E Harris
University of Virginia · US

Funding

TRAINING IN THE PHARMACOLOGICAL SCIENCEST32GM007055 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LYNCH, KEVIN R. · 1985 to 2022
$7.2M
Atomic Force MicroscopeS10RR026490 · NCRR · UNIVERSITY OF VIRGINIA · PI CREUTZ, CARL E · 2010 to 2010
$203k
NCRR NIH HHS S10 RR026490NCRR NIH HHS S10-RR026490NIGMS NIH HHS T32 GM007055
6 · The paper itself

Abstract

Lipins are phosphatidic acid phosphatases involved in the biosynthesis of triacylglycerols and phospholipids. They are associated with the endoplasmic reticulum but can also travel into the nucleus and alter gene expression. Previous studies indicate lipins in solution form high molecular weight complexes, possibly tetramers. This study was undertaken to determine if lipins form complexes on membranes as well. Murine lipin 1b was applied to a supported bilayer of phosphatidylcholine, phosphatidylserine, and cholesterol and examined by atomic force microscopy (AFM) over time. Lipin on bare mica appeared as a symmetric particle with a volume consistent with the size of a monomer. On the bilayer, lipin initially bound as asymmetric, curved particles that sometimes assembled into circular structures with an open center. Subsequently, lipin assemblies grew into large, symmetric particles with an average volume 12 times that of the monomer. Over time, some of the lipin assemblies were removed from the bilayer by the AFM probe leaving behind "footprints" composed of complex patterns that may reflect the substructure of the lipin assemblies. The lipin complexes appeared very flat, with a diameter 20 times their height. The footprints had a similar diameter, providing confirmation of the extensive deformation of the protein under the AFM probe. The ability of lipin to form large complexes on membranes may have significant implications for the local concentrations of the product, diacylglycerol, formed during hydrolysis of phosphatidic acid and for cooperative hormonal regulation of lipin activity through phosphorylation of one or more monomers in the complexes.

Indexed as

AnimalsCalcium ChlorideCholesterolIndicators and ReagentsKineticsLipid BilayersMiceMicroscopy, Atomic ForceMolecular WeightNuclear ProteinsPhosphatidate PhosphatasePhosphatidylcholinesPhosphatidylserinesProtein ConformationProtein DenaturationRecombinant ProteinsCalcium ChlorideCholesterolIndicators and ReagentsLipid BilayersLpin1 protein, mouseNuclear ProteinsPhosphatidate PhosphatasePhosphatidylcholinesPhosphatidylserinesRecombinant Proteins

Identifiers

PMID23862673
PMCPMC4041088
OpenAlexW2052847246

What OpenQuestion holds

Textmetadata
LicenceTDM
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.