4.5 Article

A novel array-based assay of in situ tissue transglutaminase activity in human umbilical vein endothelial cells

Journal

ANALYTICAL BIOCHEMISTRY
Volume 394, Issue 2, Pages 217-222

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2009.07.040

Keywords

In situ transglutaminase; Protein array; Reproducibility; Maitotoxin; Human umbilical vein endothelial cells

Funding

  1. Ministry of Health, Welfare, and Family Affairs [A030003]
  2. Basic Research Program of the Korean Science and Engineering Foundation (KOSEF) [2008-05943]

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Transglutaminases (TGs), a family of calcium-dependent transamidating enzymes, are involved in functions such as apoptosis and inflammation and play a role in autoimmune diseases and neurodegenerative disorders. In this study, we describe a novel array-based approach to rapidly determine in situ TG activity in human umbilical vein endothelial cells and J82 human bladder carcinoma cells. Amine arrays were fabricated by immobilizing 3-aminopropyltrimethoxysilane on glass slides. The assay was specific and highly reproducible. The average coefficient of variation betweens spots was 2.6% (n = 3 arrays), and the average correlation coefficients between arrays and between arrays/reactions were 0.998 and 0.976, respectively (n = 3 arrays). The assay was successfully applied to detect changes in TG activity induced by maitotoxin and to analyze inhibition of the TG activation with cystamine and monodansyl cadaverine. In addition, the assay demonstrated that intracellular reactive oxygen species regulate the maitotoxin-induced activation of TG. Thus, the array-based in situ TG activity assay constitutes a rapid and high-throughput approach to investigating the roles of TGs in cell signaling. (C) 2009 Elsevier Inc. All rights reserved.

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