Evidence map›Paper›PMID 16899541›Full record

ArticleMolecular & cellular proteomics : MCP2006

LC-MS/MS analysis of apical and basolateral plasma membranes of rat renal collecting duct cells.

Ming-Jiun Yu, Trairak Pisitkun, Guanghui Wang, Rong-Fong Shen, Mark A Knepper

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.5field-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

33 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Flow resistance along the rat renal tubule.American journal of physiology. Renal physiology · 2018
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Quantitative apical membrane proteomics reveals vasopressin-induced actin dynamics in collecting duct cells.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  17. Vasopressin inhibits apoptosis in renal collecting duct cells.American journal of physiology. Renal physiology · 2013
    Article
  18. Gene expression databases for kidney epithelial cells.American journal of physiology. Renal physiology · 2012
    Review
  19. Article
  20. c-Abl mediates high NaCl-induced phosphorylation and activation of the transcription factor TonEBP/OREBP.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    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

5 authors at 2 institutions in 1 country.

Ming-Jiun YuLaboratory of Kidney and Electrolyte Metabolism, NHLBI, National Institutes of Health, Bethesda, Maryland 20892, USA.
Trairak Pisitkun
Guanghui Wang
Rong-Fong Shen
Mark A Knepper
National Institutes of Health · USNational Heart Lung and Blood Institute · US

Funding

SOLUTE AND WATER TRANSPORT IN RENAL EPITHELIAZ01HL001285 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI KNEPPER, MARK A · 1998 to 2008
$3.8M
Intramural NIH HHS Z01 HL001285Intramural NIH HHS Z99 HL999999NHLBI NIH HHS Z01-HL-01285-KE
6 · The paper itself

Abstract

We used biotinylation and streptavidin affinity chromatography to label and enrich proteins from apical and basolateral membranes of rat kidney inner medullary collecting ducts (IMCDs) prior to LC-MS/MS protein identification. To enrich apical membrane proteins and bound peripheral membrane proteins, IMCDs were perfusion-labeled with primary amine-reactive biotinylation reagents at 2 degrees C using a double barreled pipette. The perfusion-biotinylated proteins and proteins bound to them were isolated with CaptAvidin-agarose beads, separated with SDS-PAGE, and sliced into continuous gel pieces for LC-MS/MS protein identification (LTQ, Thermo Electron Corp.). 17 integral and glycosylphosphatidylinositol (GPI)-linked membrane proteins and 44 non-integral membrane proteins were identified. Immunofluorescence confocal microscopy confirmed ACVRL1, H(+)/K(+)-ATPase alpha1, NHE2, and TauT expression in the IMCDs. Basement membrane and basolateral membrane proteins were biotinylated via incubation of IMCD suspensions with biotinylation reagents on ice. 23 integral and GPI-linked membrane proteins and 134 non-integral membrane proteins were identified. Analyses of non-integral membrane proteins preferentially identified in the perfusion-biotinylated and not in the incubation-biotinylated IMCDs revealed protein kinases, scaffold proteins, SNARE proteins, motor proteins, small GTP-binding proteins, and related proteins that may be involved in vasopressin-stimulated AQP2, UT-A1, and ENaC regulation. A World Wide Web-accessible database was constructed of 222 membrane proteins (integral and GPI-linked) from this study and prior studies.

Indexed as

AnimalsBiotinylationCell MembraneChromatography, LiquidKidney MedullaKidney Tubules, CollectingMaleMass SpectrometryMembrane ProteinsProteomeRatsRats, Sprague-DawleyMembrane ProteinsProteome

Identifiers

PMID16899541
PMCPMC2412072
OpenAlexW2118265835

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.