Literature DB >> 22933318

Chemical biology for understanding matrix metalloproteinase function.

Anna Knapinska1, Gregg B Fields.   

Abstract

The matrix metalloproteinase (MMP) family has long been associated with normal physiological processes such as embryonic implantation, tissue remodeling, organ development, and wound healing, as well as multiple aspects of cancer initiation and progression, osteoarthritis, inflammatory and vascular diseases, and neurodegenerative diseases. The development of chemically designed MMP probes has advanced our understanding of the roles of MMPs in disease in addition to shedding considerable light on the mechanisms of MMP action. The first generation of protease-activated agents has demonstrated proof of principle as well as providing impetus for in vivo applications. One common problem has been a lack of agent stability at nontargeted tissues and organs due to activation by multiple proteases. The present review considers how chemical biology has impacted the progress made in understanding the roles of MMPs in disease and the basic mechanisms of MMP action.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22933318      PMCID: PMC3951272          DOI: 10.1002/cbic.201200298

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  128 in total

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Review 3.  Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases.

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4.  Proteolytic profiling of the extracellular matrix degradome.

Authors:  Diane Baronas-Lowell; Janelle L Lauer-Fields; Mohammad Al-Ghoul; Gregg B Fields
Journal:  Methods Mol Biol       Date:  2007

Review 5.  Human matrix metalloproteinase specificity studies using collagen sequence-based synthetic peptides.

Authors:  H Nagase; G B Fields
Journal:  Biopolymers       Date:  1996       Impact factor: 2.505

6.  Rapid identification of highly active and selective substrates for stromelysin and matrilysin using bacteriophage peptide display libraries.

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Journal:  J Biol Chem       Date:  1995-03-24       Impact factor: 5.157

7.  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

8.  Discovering disease-associated enzymes by proteome reactivity profiling.

Authors:  Katherine T Barglow; Benjamin F Cravatt
Journal:  Chem Biol       Date:  2004-11

9.  Matrix metalloproteinase triple-helical peptidase activities are differentially regulated by substrate stability.

Authors:  Dmitriy Minond; Janelle L Lauer-Fields; Hideaki Nagase; Gregg B Fields
Journal:  Biochemistry       Date:  2004-09-14       Impact factor: 3.162

10.  Diffusion of MMPs on the surface of collagen fibrils: the mobile cell surface-collagen substratum interface.

Authors:  Ivan E Collier; Wesley Legant; Barry Marmer; Olga Lubman; Saveez Saffarian; Tetsuro Wakatsuki; Elliot Elson; Gregory I Goldberg
Journal:  PLoS One       Date:  2011-09-01       Impact factor: 3.240

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  19 in total

Review 1.  Extracellular Matrix Reorganization During Wound Healing and Its Impact on Abnormal Scarring.

Authors:  Meilang Xue; Christopher J Jackson
Journal:  Adv Wound Care (New Rochelle)       Date:  2015-03-01       Impact factor: 4.730

Review 2.  Architecture and function of metallopeptidase catalytic domains.

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Journal:  Protein Sci       Date:  2014-02       Impact factor: 6.725

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Review 4.  Future nanomedicine for the diagnosis and treatment of osteoarthritis.

Authors:  Lauren R Eichaker; Hongsik Cho; Craig L Duvall; Thomas A Werfel; Karen A Hasty
Journal:  Nanomedicine (Lond)       Date:  2014-07       Impact factor: 5.307

5.  Near-infrared triple-helical peptide with quenched fluorophores for optical imaging of MMP-2 and MMP-9 proteolytic activity in vivo.

Authors:  Xuan Zhang; Jamee Bresee; Gregg B Fields; W Barry Edwards
Journal:  Bioorg Med Chem Lett       Date:  2014-07-05       Impact factor: 2.823

6.  The role of collagen charge clusters in the modulation of matrix metalloproteinase activity.

Authors:  Janelle L Lauer; Manishabrata Bhowmick; Dorota Tokmina-Roszyk; Yan Lin; Steven R Van Doren; Gregg B Fields
Journal:  J Biol Chem       Date:  2013-12-02       Impact factor: 5.157

7.  Coupling protein engineering with probe design to inhibit and image matrix metalloproteinases with controlled specificity.

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8.  DNA methyltransferase genes polymorphisms are associated with primary knee osteoarthritis: a matched case-control study.

Authors:  Antonio Miranda-Duarte; Verónica Marusa Borgonio-Cuadra; Norma Celia González-Huerta; Emma Xochitl Rojas-Toledo; Juan Francisco Ahumada-Pérez; Matvey Sosa-Arellano; Eugenio Morales-Hernández; Nonanzit Pérez-Hernández; José Manuel Rodríguez-Pérez
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9.  TAGLN suppresses proliferation and invasion, and induces apoptosis of colorectal carcinoma cells.

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10.  MT1-MMP activatable fluorogenic probes with enhanced specificity via high-affinity peptide conjugation for tumor imaging.

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Journal:  Biomater Sci       Date:  2020-03-18       Impact factor: 6.843

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