| Literature DB >> 20659604 |
Marta Sikora1, Lukasz Marczak, Tomasz Twardowski, Maciej Stobiecki, Hieronim Jakubowski.
Abstract
A posttranslational protein modification by homocysteine-thiolactone (N-homocysteinylation) is linked to human vascular and neurodegenerative diseases. Although chemical and immunological methods are available to detect and quantify the extent of protein N-homocysteinylation, the determination of site-specific N-homocysteinylation in vivo remains challenging. Here we describe a liquid chromatography/mass spectrometry method that monitors the extent of N-homocysteinylation at albumin lysine-525 in vivo directly in human serum. Using this method, we found that the extent of lysine-525 N-homocysteinylation was significantly increased in patients with cystathionine beta-synthase deficiency. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20659604 DOI: 10.1016/j.ab.2010.04.034
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365