Evidence map›Paper›PMID 19956408›Full record

ArticleMolecular vision2009

The membrane proteome of the mouse lens fiber cell.

Steven Bassnett, Phillip A Wilmarth, Larry L David

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing 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

89 citing papers in PubMed, 113 citations in OpenAlex.

  1. CatExperimental eye research · 2026
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  18. The aging mouse lens transcriptome.Experimental eye research · 2021
    Article
  19. Article
  20. Article

29 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Steven BassnettOphthalmology & Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA. Bassnett@vision.wustl.edu
Phillip A Wilmarth
Larry L David
Washington University in St. Louis · US

Funding

Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TED S ACOTT · 1995 to 2026
$19.4M
WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Philip Andrew Ruzycki · 1985 to 2026
$18.4M
PROTEIN CLEAVAGE SITES IN EXPERIMENTAL CATARACTOUS LENSR01EY007755 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DAVID, LARRY L · 1995 to 2014
$3.6M
LIM2 AND THE LENS CORE SYNCYTIUMR01EY018185 · NEI · WASHINGTON UNIVERSITY · PI BASSNETT, STEVEN · 2008 to 2012
$1.9M
NEI NIH HHS P30EY00268NEI NIH HHS P30 EY002687NEI NIH HHS P30 EY010572NEI NIH HHS P30EY010572NEI NIH HHS R01 EY007755NEI NIH HHS R01EY007755NEI NIH HHS R01 EY018185NEI NIH HHS R01EY018185
6 · The paper itself

Abstract

purposeFiber cells of the ocular lens are bounded by a highly specialized plasma membrane. Despite the pivotal role that membrane proteins play in the physiology and pathophysiology of the lens, our knowledge of the structure and composition of the fiber cell plasma membrane remains fragmentary. In the current study, we utilized mass spectrometry-based shotgun proteomics to provide a comprehensive survey of the mouse lens fiber cell membrane proteome.

methodsMembranes were purified from young mouse lenses and subjected to MudPIT (Multidimensional protein identification technology) analysis. The resulting proteomic data were analyzed further by reference to publically available microarray databases.

resultsMore than 200 membrane proteins were identified by MudPIT, including Type I, Type II, Type III (multi-pass), lipid-anchored, and GPI-anchored membrane proteins, in addition to membrane-associated cytoskeletal elements and extracellular matrix components. The membrane proteins of highest apparent abundance included Mip, Lim2, and the lens-specific connexin proteins Gja3, Gja8, and Gje1. Significantly, many proteins previously unsuspected in the lens were also detected, including proteins with roles in cell adhesion, solute transport, and cell signaling.

conclusionsThe MudPIT technique constitutes a powerful technique for the analysis of the lens membrane proteome and provides valuable insights into the composition of the lens fiber cell unit membrane.

Indexed as

AnimalsCell AdhesionCell MembraneCytoskeletonExtracellular MatrixIon ChannelsIon PumpsLens, CrystallineMiceMice, Inbred C57BLProteomeras ProteinsSignal TransductionIon ChannelsIon PumpsProteomeras Proteins

Identifiers

PMID19956408
PMCPMC2786885
OpenAlexW2129265219

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.