| Literature DB >> 22210513 |
Nadine Kaesler1, Thomas Schettgen, Vasantha P Mutucumarana, Vincent Brandenburg, Willi Jahnen-Dechent, Leon J Schurgers, Thilo Krüger.
Abstract
The gamma (γ)-glutamyl carboxylase is a key enzyme in vitamin K-dependent carboxylation of proteins involved in hemostasis and inflammation. It is an endoplasmic enzyme posttranslationally converting glutamic acid residues into γ-carboxyglutamic acid residues in proteins. The activity of tissue derived γ-glutamyl carboxylase is commonly assayed by incorporation of H¹⁴CO₃⁻ into synthetic peptides and subsequent quantification using liquid scintillation counting. We present a nonradioactive assay using a fluorescein isothiocyanate-labeled short peptide that can be readily detected in its unmodified and γ-glutamyl carboxylated form by reversed-phase HPLC. This method offers a convenient alternative to the established radioactive labeling techniques.Entities:
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Year: 2011 PMID: 22210513 DOI: 10.1016/j.ab.2011.11.036
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365