Literature DB >> 22210513

A fluorescent method to determine vitamin K-dependent gamma-glutamyl carboxylase activity.

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.
Copyright © 2011 Elsevier Inc. All rights reserved.

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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


  2 in total

1.  Functional Study of the Vitamin K Cycle Enzymes in Live Cells.

Authors:  J-K Tie; D W Stafford
Journal:  Methods Enzymol       Date:  2016-11-22       Impact factor: 1.600

2.  Effect of Vitamin K on Vascular Health and Physical Function in Older People with Vascular Disease--A Randomised Controlled Trial.

Authors:  R L Fulton; M E T McMurdo; A Hill; R J Abboud; G P Arnold; A D Struthers; F Khan; C Vermeer; M H J Knapen; N E A Drummen; M D Witham
Journal:  J Nutr Health Aging       Date:  2016-03       Impact factor: 4.075

  2 in total

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