Literature DB >> 12669115

The ADAMs family of proteins: from basic studies to potential clinical applications.

Michael J Duffy1, David J Lynn, Andrew T Lloyd, Caroline M O'Shea.   

Abstract

The ADAMs are a family of membrane proteins possessing a disintegrin and metalloprotease domain. Currently, 34 members are known to exist. Approximately 50% of the ADAMs contain a metalloprotease-like domain and some of these have been shown to possess protease activity. Most of the protein substrates identified to date for ADAMs are either integral membrane or extracellular matrix (ECM) proteins. In addition to hydrolysing proteins, a number of ADAMs bind to integrins. The attachment to integrins occurs via the disintegrin domain. Since the ADAMs can play a role in both proteolysis and adhesion, they have been implicated in a variety of biological processes such as sperm-egg fusion, somatic cell-cell adhesion, ectodomain shedding, myoblast fusion and development. Altered expression of certain ADAMs has been associated with a number of diseases including asthma, arthritis, Alzheimer's disease, atherosclerosis and cancer.

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Year:  2003        PMID: 12669115

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  16 in total

1.  Crystallization and preliminary X-ray crystallographic analysis of two vascular apoptosis-inducing proteins (VAPs) from Crotalus atrox venom.

Authors:  Tomoko Igarashi; Yuko Oishi; Satohiko Araki; Hidezo Mori; Soichi Takeda
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2006-06-26

2.  Crystal structures of VAP1 reveal ADAMs' MDC domain architecture and its unique C-shaped scaffold.

Authors:  Soichi Takeda; Tomoko Igarashi; Hidezo Mori; Satohiko Araki
Journal:  EMBO J       Date:  2006-05-11       Impact factor: 11.598

3.  Modulation of innate immune responses with synthetic lipid A derivatives.

Authors:  Yanghui Zhang; Jidnyasa Gaekwad; Margreet A Wolfert; Geert-Jan Boons
Journal:  J Am Chem Soc       Date:  2007-03-29       Impact factor: 15.419

4.  Role of ADAMs in endothelial cell permeability: cadherin shedding and leukocyte rolling.

Authors:  Bharathy Ponnuchamy; Raouf A Khalil
Journal:  Circ Res       Date:  2008-05-23       Impact factor: 17.367

5.  Structural characterization of the ectodomain of a disintegrin and metalloproteinase-22 (ADAM22), a neural adhesion receptor instead of metalloproteinase: insights on ADAM function.

Authors:  Heli Liu; Ann H R Shim; Xiaolin He
Journal:  J Biol Chem       Date:  2009-08-18       Impact factor: 5.157

6.  Tumor imaging by means of proteolytic activation of cell-penetrating peptides.

Authors:  Tao Jiang; Emilia S Olson; Quyen T Nguyen; Melinda Roy; Patricia A Jennings; Roger Y Tsien
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-15       Impact factor: 11.205

7.  Expression of ADAM15 in lung carcinomas.

Authors:  A Schütz; W Härtig; M Wobus; J Grosche; Ch Wittekind; G Aust
Journal:  Virchows Arch       Date:  2005-03-09       Impact factor: 4.064

8.  ADAM2 interactions with mouse eggs and cell lines expressing α4/α9 (ITGA4/ITGA9) integrins: implications for integrin-based adhesion and fertilization.

Authors:  Ulyana V Desiderio; Xiaoling Zhu; Janice P Evans
Journal:  PLoS One       Date:  2010-10-29       Impact factor: 3.240

Review 9.  The ADAMs family of proteases as targets for the treatment of cancer.

Authors:  Maeve Mullooly; Patricia M McGowan; John Crown; Michael J Duffy
Journal:  Cancer Biol Ther       Date:  2016-04-26       Impact factor: 4.742

10.  The disintegrin and metalloproteinase ADAM12 contributes to TGF-beta signaling through interaction with the type II receptor.

Authors:  Azeddine Atfi; Emmanuelle Dumont; Frédéric Colland; Dominique Bonnier; Annie L'helgoualc'h; Céline Prunier; Nathalie Ferrand; Bruno Clément; Ulla M Wewer; Nathalie Théret
Journal:  J Cell Biol       Date:  2007-07-09       Impact factor: 10.539

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