Literature DB >> 14596909

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

Kei Hori1, Daijiro Konno, Hisato Maruoka, Kenji Sobue.   

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.

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Year:  2003        PMID: 14596909     DOI: 10.1016/s0014-5793(03)01074-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  12 in total

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4.  NMDA receptor-dependent synaptic translocation of insulin receptor substrate p53 via protein kinase C signaling.

Authors:  Kei Hori; Hiroki Yasuda; Daijiro Konno; Hisato Maruoka; Tadaharu Tsumoto; Kenji Sobue
Journal:  J Neurosci       Date:  2005-03-09       Impact factor: 6.167

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Journal:  J Cell Biol       Date:  2011-01-31       Impact factor: 10.539

9.  The BAR Domain Superfamily Proteins from Subcellular Structures to Human Diseases.

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Journal:  Membranes (Basel)       Date:  2012-02-27

10.  Inclusion of Scar/WAVE3 in a similar complex to Scar/WAVE1 and 2.

Authors:  Craig F Stovold; Thomas H Millard; Laura M Machesky
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