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PMID: 14596909 Published · ppublish English Journal Article

MALS is a binding partner of IRSp53 at cell-cell contacts.

FEBS letters ·Vol. 554 ·No. 1-2 ·2003-11-06 ·Pages 30-4

Hori K, Konno D, Maruoka H, Sobue K

Abstract

Insulin receptor substrate p53 (IRSp53) is a key player in cytoskeletal dynamics, interacting with the actin modulators WAVE2 and Mena. Here, we identified a PDZ protein, MALS, as an IRSp53-interacting protein using a yeast two-hybrid screen. A pull-down assay showed that IRSp53 and MALS interact through the PDZ domain of MALS and the C-terminal PDZ-binding sequence of IRSp53. Their interaction in MDCK cells was also demonstrated by co-immunoprecipitation. Immunocytochemistry showed the colocalization of IRSp53 and MALS at cell-cell contacts. Cytochalasin D induced the redistribution of both proteins to the cytosol. Thus, MALS is a partner of IRSp53 anchoring the actin-based membrane cytoskeleton at cell-cell contacts.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Carrier Proteins/metabolism Cell Communication Cytochalasin D/pharmacology Cytoskeletal Proteins/metabolism Cytoskeleton/chemistry Immunohistochemistry Membrane Proteins/metabolism Nerve Tissue Proteins/metabolism Protein Binding Rats Two-Hybrid System Techniques
Chemicals
BAIAP2 protein, human Carrier Proteins Cytoskeletal Proteins LIN7B protein, human Membrane Proteins Nerve Tissue Proteins Cytochalasin D
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hori Kei
Department of Neuroscience (D13), Osaka University Graduate School of Medicine, Yamadaoka 2-2, Suita City, Osaka, Japan.
Konno Daijiro
Maruoka Hisato
Sobue Kenji
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
2003-11-06
Pages
30-4
Language
English
Region
England
NLM ID
0155157
Subset
IM
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