Literature DB >> 31463913

Cell-Based Interaction Analysis of ADAMTS Proteases and ADAMTS-Like Proteins with Fibrillin Microfibrils.

Dirk Hubmacher1.   

Abstract

The extracellular matrix (ECM) is a composite biomaterial that serves as an anchor for cells and provides guidance cues for cell migration, proliferation, and differentiation. However, many details of the hierarchical ECM assembly process and the role of individual protein-protein interactions are not well understood. Here, I describe a cell-culture-based method that allows for determination of the ECM localization of recombinant ADAMTS proteases and ADAMTS-like (L) proteins in relationship to fibrillin microfibrils deposited by human dermal fibroblasts. The method can be readily adapted to study the localization of ECM components other than ADAMTS and ADAMTSL proteins to fibrillin microfibrils and other ECM networks.

Entities:  

Keywords:  ADAMTS proteases; ADAMTS-like proteins; Coculture assay; Extracellular matrix; Fibrillin microfibrils; Immuno-colocalization; Recombinant protein

Mesh：

Substances：

Year:  2020        PMID： 31463913      PMCID： PMC6910243          DOI： 10.1007/978-1-4939-9698-8_16

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN： 1064-3745


  22 in total

1.  Fibrillin assembly requires fibronectin.

Authors:  Laetitia Sabatier; Daliang Chen; Christine Fagotto-Kaufmann; Dirk Hubmacher; Marc D McKee; Douglas S Annis; Deane F Mosher; Dieter P Reinhardt
Journal:  Mol Biol Cell       Date:  2008-11-26       Impact factor: 4.138

Review 2.  A disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanisms.

Authors:  Suneel S Apte
Journal:  J Biol Chem       Date:  2009-09-04       Impact factor: 5.157

3.  Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.

Authors:  Carine Le Goff; Clémentine Mahaut; Lauren W Wang; Slimane Allali; Avinash Abhyankar; Sacha Jensen; Louise Zylberberg; Gwenaelle Collod-Beroud; Damien Bonnet; Yasemin Alanay; Angela F Brady; Marie-Pierre Cordier; Koen Devriendt; David Genevieve; Pelin Özlem Simsek Kiper; Hiroshi Kitoh; Deborah Krakow; Sally Ann Lynch; Martine Le Merrer; André Mégarbane; Geert Mortier; Sylvie Odent; Michel Polak; Marianne Rohrbach; David Sillence; Irene Stolte-Dijkstra; Andrea Superti-Furga; David L Rimoin; Vicken Topouchian; Sheila Unger; Bernhard Zabel; Christine Bole-Feysot; Patrick Nitschke; Penny Handford; Jean-Laurent Casanova; Catherine Boileau; Suneel S Apte; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2011-06-16       Impact factor: 11.025

4.  ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts.

Authors:  Wendy E Kutz; Lauren W Wang; Hannah L Bader; Alana K Majors; Kazushi Iwata; Elias I Traboulsi; Lynn Y Sakai; Douglas R Keene; Suneel S Apte
Journal:  J Biol Chem       Date:  2011-03-14       Impact factor: 5.157

5.  Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systems.

Authors:  Justin S Weinbaum; Thomas J Broekelmann; Richard A Pierce; Claudio C Werneck; Fernando Segade; Clarissa S Craft; Russell H Knutsen; Robert P Mecham
Journal:  J Biol Chem       Date:  2008-07-14       Impact factor: 5.157

6.  Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome.

Authors:  Lauren C Beene; Lauren W Wang; Dirk Hubmacher; Douglas R Keene; Dieter P Reinhardt; Douglas S Annis; Deane F Mosher; Robert P Mecham; Elias I Traboulsi; Suneel S Apte
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-12-23       Impact factor: 4.799

7.  ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome.

Authors:  Nathalie Dagoneau; Catherine Benoist-Lasselin; Céline Huber; Laurence Faivre; André Mégarbané; Abdulrahman Alswaid; Hélène Dollfus; Yves Alembik; Arnold Munnich; Laurence Legeai-Mallet; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2004-09-13       Impact factor: 11.025

8.  Homo- and heterotypic fibrillin-1 and -2 interactions constitute the basis for the assembly of microfibrils.

Authors:  Guoqing Lin; Kerstin Tiedemann; Tillman Vollbrandt; Hannelore Peters; Boris Batge; Jurgen Brinckmann; Dieter P Reinhardt
Journal:  J Biol Chem       Date:  2002-10-23       Impact factor: 5.157

9.  Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease.

Authors:  Dirk Hubmacher; Michael Schneider; Steven J Berardinelli; Hideyuki Takeuchi; Belinda Willard; Dieter P Reinhardt; Robert S Haltiwanger; Suneel S Apte
Journal:  Sci Rep       Date:  2017-02-08       Impact factor: 4.379

10.  Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome.

Authors:  Mohd Hussain Shah; Vishwanath Bhat; Jyoti S Shetty; Arun Kumar
Journal:  Mol Vis       Date:  2014-06-12       Impact factor: 2.367
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  1 in total

1.  Alternative splicing of the metalloprotease ADAMTS17 spacer regulates secretion and modulates autoproteolytic activity.

Authors:  Zerina Balic; Saurav Misra; Belinda Willard; Dieter P Reinhardt; Suneel S Apte; Dirk Hubmacher
Journal:  FASEB J       Date:  2021-02       Impact factor: 5.834
  1 in total

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