| Literature DB >> 23357238 |
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.Entities:
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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