Literature DB >> 23357238

A homogeneous fluorescence anisotropy assay for measuring transglutaminase 2 activity.

Jon A Kenniston1, Gregory P Conley, Daniel J Sexton, Andrew E Nixon.   

Abstract

Transglutaminases catalyze the covalent linkage of protein polypeptides through their glutamine and lysine side chains. Tissue transglutaminase 2 (TG2) has been of particular interest given its potential role in several disorders, including a variety of cancers and neurodegenerative diseases. Here we report a biochemical assay that monitors TG2 activity by following an increase in the fluorescence anisotropy of a fluorescein-labeled substrate peptide as it conjugates to a bovine serum albumin (BSA) cosubstrate of larger hydrodynamic mass. The resulting homogeneous assay is sensitive to low TG2 concentrations (pM range) and is readily adapted to higher throughput formats.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23357238     DOI: 10.1016/j.ab.2013.01.016

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  Application of a Fluorescence Anisotropy-Based Assay to Quantify Transglutaminase 2 Activity in Cell Lysates.

Authors:  Sandra Hauser; Paul Sommerfeld; Johanna Wodtke; Christoph Hauser; Paul Schlitterlau; Jens Pietzsch; Reik Löser; Markus Pietsch; Robert Wodtke
Journal:  Int J Mol Sci       Date:  2022-04-19       Impact factor: 6.208

2.  Optimised methods (SDS/PAGE and LC-MS) reveal deamidation in all examined transglutaminase-mediated reactions.

Authors:  Éva Sivadó; Meddy El Alaoui; Robert Kiraly; László Fesüs; Frédéric Delolme; Adeline Page; Saïd El Alaoui
Journal:  FEBS Open Bio       Date:  2019-01-18       Impact factor: 2.693

3.  Biotechnological applications of transglutaminases.

Authors:  Natalie M Rachel; Joelle N Pelletier
Journal:  Biomolecules       Date:  2013-10-22
  3 in total

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