Evidence map›Paper›PMID 19856143›Full record

ArticleCellular and molecular life sciences : CMLS2010

Inactivation of the proximal NPXY motif impairs early steps in LRP1 biosynthesis.

Sara M Reekmans, Thorsten Pflanzner, Philip L S M Gordts, Simone Isbert, Pascale Zimmermann, Wim Annaert, Sascha Weggen, Anton J M Roebroek, Claus U Pietrzik

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

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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

9 authors at 5 institutions in 2 countries.

Sara M ReekmansLaboratory for Experimental Mouse Genetics, Center for Human Genetics, KU Leuven, Herestraat, Leuven, Belgium.
Thorsten Pflanzner
Philip L S M Gordts
Simone Isbert
Pascale Zimmermann
Wim Annaert
Sascha Weggen
Anton J M Roebroek
Claus U Pietrzik
KU Leuven · BEUniversity Medical Center of the Johannes Gutenberg University Mainz · DEVIB-KU Leuven Center for Cancer Biology · BEHeinrich Heine University Düsseldorf · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proximal NPXY and distal NPXYXXL motifs in the intracellular domain of LRP1 play an important role in regulation of the function of the receptor. The impact of single and double inactivating knock-in mutations of these motifs on receptor maturation, cell surface expression, and ligand internalization was analyzed in mutant and control wild-type mice and MEFs. Single inactivation of the proximal NPXY or in combination with inactivation of the distal NPXYXXL motif are both shown to be associated with an impaired maturation and premature proteasomal degradation of full-length LRP1. Therefore, only a small mature LRP1 pool is able to reach the cell surface resulting indirectly in severe impairment of ligand internalization. Single inactivation of the NPXYXXL motif revealed normal maturation, but direct impairment of ligand internalization. In conclusion, the proximal NPXY motif proves to be essential for early steps in the LRP1 biosynthesis, whereas NPXYXXL appears rather relevant for internalization.

Indexed as

Amino Acid MotifsAnimalsEmbryonic DevelopmentEndocytosisGene Knock-In TechniquesLow Density Lipoprotein Receptor-Related Protein-1MiceMutationProteasome Endopeptidase ComplexProtein Interaction Domains and MotifsProtein Structure, TertiaryReceptors, LDLSurvival AnalysisTumor Suppressor ProteinsLow Density Lipoprotein Receptor-Related Protein-1Lrp1 protein, mouseProteasome Endopeptidase ComplexReceptors, LDLTumor Suppressor Proteins

Identifiers

PMID19856143
PMCPMC11115674
OpenAlexW2163781955

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.