| Literature DB >> 17716614 |
Albert J W Zendman1, Reinout Raijmakers, Suzanne Nijenhuis, Erik R Vossenaar, Marloes van den Tillaart, Renato G S Chirivi, Jos M H Raats, Walther J van Venrooij, Jan W Drijfhout, Ger J M Pruijn.
Abstract
Members of the family of peptidylarginine deiminases (PADs, EC 3.5.3.15) catalyze the posttranslational modification of peptidylarginine into peptidylcitrulline. Citrulline-containing epitopes have been shown to be major and specific targets of autoantibodies produced by rheumatoid arthritis patients. Recently, the citrullination of histone proteins by PAD enzyme was reported to influence gene expression levels. These findings greatly increase the interest in the PAD enzymes and their activities. A few procedures to monitor PAD activity in biological samples have been described previously. However, these assays either have low sensitivity or are rather laborious. Here we describe a reliable and reproducible method for the determination of PAD activity in both purified and crude samples. The method is based on the quantification of PAD-dependent citrullination of peptides, immobilized in microtiter plates, using antibodies that are exclusively reactive with the reaction product(s). Our results demonstrate that this antibody-based assay for PAD activity, called ABAP, is very sensitive and can be applied to monitor PAD activity in biological samples.Entities:
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Year: 2007 PMID： 17716614 DOI： 10.1016/j.ab.2007.07.009
Source DB: PubMed Journal: Anal Biochem ISSN： 0003-2697 Impact factor: 3.365