Literature DB >> 15946988

Palmitoylation at Cys574 is essential for MT1-MMP to promote cell migration.

Narayanapanicker Anilkumar1, Takamasa Uekita, John R Couchman, Hideaki Nagase, Motoharu Seiki, Yoshifumi Itoh.   

Abstract

MT1-MMP is a type I transmembrane proteinase that promotes cell migration and invasion. Here, we report that MT1-MMP is palmitoylated at Cys574 in the cytoplasmic domain, and this lipid modification is critical for its promotion of cell migration and clathrin-mediated internalization. The palmitoylation-defective mutant (C574A) failed to promote cell migration and was not internalized through clathrin pathway like wild-type, but it was internalized through the caveolae pathway. Reintroducing a cysteine at different positions in the cytoplasmic tail of the C574A mutant revealed that the position of the palmitoylated cysteine relative to LLY573, a motif that interacts with mu2 subunit of adaptor protein 2, is critical for the cell motility-promoting activity of MT1-MMP and its clathrin-mediated internalization. Taken together, palmitoylation of MT1-MMP is one of the key posttranslational modifications that determines MT1-MMP-dependent cell migration.

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Year:  2005        PMID: 15946988     DOI: 10.1096/fj.04-3651fje

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  30 in total

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Journal:  Arthritis Rheum       Date:  2010-05

2.  Membrane type 1 matrix metalloproteinase (MT1-MMP) ubiquitination at Lys581 increases cellular invasion through type I collagen.

Authors:  Patricia A Eisenach; Pedro Corrêa de Sampaio; Gillian Murphy; Christian Roghi
Journal:  J Biol Chem       Date:  2012-02-07       Impact factor: 5.157

3.  Posttranslational regulation of membrane type 1-matrix metalloproteinase (MT1-MMP) in mouse PTEN null prostate cancer cells: Enhanced surface expression and differential O-glycosylation of MT1-MMP.

Authors:  Seaho Kim; Wei Huang; Emilio P Mottillo; Anjum Sohail; Yoon-Ah Ham; M Katie Conley-Lacomb; Chong Jai Kim; Guri Tzivion; Hyeong-Reh Choi Kim; Shihua Wang; Yong Q Chen; Rafael Fridman
Journal:  Biochim Biophys Acta       Date:  2010-07-08

4.  Metalloproteinase binding proteins: WO2009097397.

Authors:  Yoshifumi Itoh
Journal:  Expert Opin Ther Pat       Date:  2010-08       Impact factor: 6.674

5.  Protein Lipidation: Occurrence, Mechanisms, Biological Functions, and Enabling Technologies.

Authors:  Hong Jiang; Xiaoyu Zhang; Xiao Chen; Pornpun Aramsangtienchai; Zhen Tong; Hening Lin
Journal:  Chem Rev       Date:  2018-01-02       Impact factor: 60.622

6.  Cell surface collagenolysis requires homodimerization of the membrane-bound collagenase MT1-MMP.

Authors:  Yoshifumi Itoh; Noriko Ito; Hideaki Nagase; Richard D Evans; Sarah A Bird; Motoharu Seiki
Journal:  Mol Biol Cell       Date:  2006-10-18       Impact factor: 4.138

7.  Characterization and regulation of MT1-MMP cell surface-associated activity.

Authors:  Sonia Pahwa; Manishabrata Bhowmick; Sabrina Amar; Jian Cao; Alex Y Strongin; Rafael Fridman; Stephen J Weiss; Gregg B Fields
Journal:  Chem Biol Drug Des       Date:  2018-12-19       Impact factor: 2.817

8.  The lectin concanavalin-A signals MT1-MMP catalytic independent induction of COX-2 through an IKKgamma/NF-kappaB-dependent pathway.

Authors:  Asmaa Sina; Sébastien Proulx-Bonneau; Alain Roy; Laurent Poliquin; Jian Cao; Borhane Annabi
Journal:  J Cell Commun Signal       Date:  2010-01-27       Impact factor: 5.782

9.  Peptide aptamers as new tools to modulate clathrin-mediated internalisation--inhibition of MT1-MMP internalisation.

Authors:  Rochana D Wickramasinghe; Paul Ko Ferrigno; Christian Roghi
Journal:  BMC Cell Biol       Date:  2010-07-23       Impact factor: 4.241

10.  The second dimer interface of MT1-MMP, the transmembrane domain, is essential for ProMMP-2 activation on the cell surface.

Authors:  Yoshifumi Itoh; Noriko Ito; Hideaki Nagase; Motoharu Seiki
Journal:  J Biol Chem       Date:  2008-03-12       Impact factor: 5.157

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