Literature DB >> 25603365

Proteomic approaches to uncover MMP function.

Pascal Schlage1, Ulrich auf dem Keller2.   

Abstract

Proteomics has revolutionized protease research and particularly contributed to the identification of novel substrates and their sites of cleavage as key determinants of protease function. New technologies and rapid advancements in development of powerful mass spectrometers allowed unprecedented insights into activities of matrix metalloproteinases (MMPs) within their complex extracellular environments. Mass spectrometry-based proteomics extended our knowledge on MMP cleavage specificities and will help to develop more specific inhibitors as new therapeutics. Quantitative proteomics and N-terminal enrichment strategies have revealed numerous novel MMP substrates and shed light on their modes of action in vitro and in vivo. In this review, we provide an overview of current proteomic technologies in protease research and their application to the functional characterization of MMPs.
Copyright © 2015. Published by Elsevier B.V.

Keywords:  Degradomics; Matrix metalloproteinases; Proteomics; TAILS; iTRAQ

Mesh:

Substances:

Year:  2015        PMID: 25603365     DOI: 10.1016/j.matbio.2015.01.003

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  14 in total

Review 1.  Matrix metalloproteinases in emphysema.

Authors:  Sina A Gharib; Anne M Manicone; William C Parks
Journal:  Matrix Biol       Date:  2018-03-23       Impact factor: 11.583

2.  Riding the metalloproteinase roller coaster.

Authors:  Gillian Murphy
Journal:  J Biol Chem       Date:  2017-03-15       Impact factor: 5.157

Review 3.  Matrix Metalloproteinases During Axonal Regeneration, a Multifactorial Role from Start to Finish.

Authors:  Lien Andries; Inge Van Hove; Lieve Moons; Lies De Groef
Journal:  Mol Neurobiol       Date:  2016-02-29       Impact factor: 5.590

4.  Site-specific O-Glycosylation by Polypeptide N-Acetylgalactosaminyltransferase 2 (GalNAc-transferase T2) Co-regulates β1-Adrenergic Receptor N-terminal Cleavage.

Authors:  Christoffer K Goth; Hanna E Tuhkanen; Hamayun Khan; Jarkko J Lackman; Shengjun Wang; Yoshiki Narimatsu; Lasse H Hansen; Christopher M Overall; Henrik Clausen; Katrine T Schjoldager; Ulla E Petäjä-Repo
Journal:  J Biol Chem       Date:  2017-02-06       Impact factor: 5.157

Review 5.  Monitoring proteolytic processing events by quantitative mass spectrometry.

Authors:  Mariel Coradin; Kelly R Karch; Benjamin A Garcia
Journal:  Expert Rev Proteomics       Date:  2017-04-17       Impact factor: 3.940

6.  High-Throughput Multiplexed Peptide-Centric Profiling Illustrates Both Substrate Cleavage Redundancy and Specificity in the MMP Family.

Authors:  Muskan Kukreja; Sergey A Shiryaev; Piotr Cieplak; Norihito Muranaka; David A Routenberg; Andrei V Chernov; Sonu Kumar; Albert G Remacle; Jeffrey W Smith; Igor A Kozlov; Alex Y Strongin
Journal:  Chem Biol       Date:  2015-08-06

Review 7.  The extracellular matrix: Tools and insights for the "omics" era.

Authors:  Alexandra Naba; Karl R Clauser; Huiming Ding; Charles A Whittaker; Steven A Carr; Richard O Hynes
Journal:  Matrix Biol       Date:  2015-07-08       Impact factor: 11.583

Review 8.  Spatial-omics: Novel approaches to probe cell heterogeneity and extracellular matrix biology.

Authors:  Grace C Bingham; Fred Lee; Alexandra Naba; Thomas H Barker
Journal:  Matrix Biol       Date:  2020-05-19       Impact factor: 10.447

9.  Expanding the Activity of Tissue Inhibitors of Metalloproteinase (TIMP)-1 against Surface-Anchored Metalloproteinases by the Replacement of Its C-Terminal Domain: Implications for Anti-Cancer Effects.

Authors:  Jing Xian Duan; Magdalini Rapti; Anastasia Tsigkou; Meng Huee Lee
Journal:  PLoS One       Date:  2015-08-26       Impact factor: 3.240

10.  Peptidase specificity from the substrate cleavage collection in the MEROPS database and a tool to measure cleavage site conservation.

Authors:  Neil D Rawlings
Journal:  Biochimie       Date:  2015-10-21       Impact factor: 4.079

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