Evidence map›Paper›PMID 16881872›Full record

ArticleThe Biochemical journal2006

Protein 4.1R self-association: identification of the binding domain.

Carmen M Pérez-Ferreiro, Eva Lospitao, Isabel Correas

Abstract read
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Article in The Biochemical journal, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Carmen M Pérez-FerreiroDepartamento de Biología Molecular, CBMSO (Centro de Biología Molecular Severo Ochoa), UAM/CSIC, Cantoblanco, E-28049 Madrid, Spain. cmperez@cbm.uam.es
Eva Lospitao
Isabel Correas

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erythroid protein 4.1 (4.1R) stabilizes the spectrin-actin network and anchors it to the plasma membrane. To contribute to the characterization of non-erythroid protein 4.1R, we used sedimentation, pull-down and co-immunoprecipitation assays to investigate the ability of protein 4.1R to establish inter-/intra-molecular associations. We demonstrated that the small 4.1R isoforms of 60 kDa (4.1R60), but not the larger isoforms of 80 and 135 kDa (4.1R80 and 4.1R135), were self-associated, and that a domain contained in all 4.1R isoforms, the core region, was responsible for 4.1R self-association. Results from denaturing-renaturing experiments, in which an initially non-self-associated 4.1R80 isoform became self-associated, suggested that an initially hidden core region was subsequently exposed. This hypothesis was supported by results from pull-down assays, which showed that the core region interacted with the N-terminal end of the FERM (4.1, ezrin, radixin, moesin) domain that is present in 4.1R80 and 4.1R135 isoforms but absent from 4.1R60 isoforms. Consistently, 4.1R80 isoforms bound neither to each other nor to 4.1R60 isoforms. We propose that 4.1R60 isoforms are constitutively self-associated, whereas 4.1R80 and 4.1R135 self-association is prevented by intramolecular interactions.

Indexed as

AnimalsBinding SitesBlood ProteinsChlorocebus aethiopsCOS CellsCytoskeletal ProteinsMembrane ProteinsMicrotubule-Associated ProteinsModels, MolecularProtein BindingProtein DenaturationProtein IsoformsProtein Structure, TertiaryBlood ProteinsCytoskeletal Proteinserythrocyte membrane band 4.1 proteinMembrane ProteinsMicrotubule-Associated ProteinsProtein Isoforms

Identifiers

PMID16881872
PMCPMC1698608

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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.