Rapid reverse phase-HPLC assay of HMG-CoA reductase activity

Radioisotope-based and mass spectrometry coupled to chromatographic techniques are the conventional methods for monitoring HMG-CoA reductase (HMGR) activity. Irrespective of offering adequate sensitivity, these methods are often cumbersome and time-consuming, requiring the handling of radiolabeled c...

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Main Authors: Matteo Mozzicafreddo, Massimiliano Cuccioloni, Anna Maria Eleuteri, Mauro Angeletti
Format: Article
Language:English
Published: Elsevier 2010-08-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520370838
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spelling doaj-917ab729ce8648c584331d7817ca13c92021-04-28T06:01:48ZengElsevierJournal of Lipid Research0022-22752010-08-0151824602463Rapid reverse phase-HPLC assay of HMG-CoA reductase activityMatteo Mozzicafreddo0Massimiliano Cuccioloni1Anna Maria Eleuteri2Mauro Angeletti3To whom correspondence should be addressed; School of Biosciences and Biotechnology, University of Camerino, Camerino (MC), ItalySchool of Biosciences and Biotechnology, University of Camerino, Camerino (MC), ItalySchool of Biosciences and Biotechnology, University of Camerino, Camerino (MC), ItalySchool of Biosciences and Biotechnology, University of Camerino, Camerino (MC), ItalyRadioisotope-based and mass spectrometry coupled to chromatographic techniques are the conventional methods for monitoring HMG-CoA reductase (HMGR) activity. Irrespective of offering adequate sensitivity, these methods are often cumbersome and time-consuming, requiring the handling of radiolabeled chemicals or elaborate ad-hoc derivatizing procedures. We propose a rapid and versatile reverse phase-HPLC method for assaying HMGR activity capable of monitoring the levels of both substrates (HMG-CoA and NADPH) and products (CoA, mevalonate, and NADP+) in a single 20 min run with no pretreatment required. The linear dynamic range was 10–26 pmol for HMG-CoA, 7–27 nmol for NADPH, 0.5–40 pmol for CoA and mevalonate, and 2–27 nmol for NADP+, and limit of detection values were 2.67 pmol, 2.77 nmol, 0.27 pmol, and 1.3 nmol, respectively.http://www.sciencedirect.com/science/article/pii/S0022227520370838
collection DOAJ
language English
format Article
sources DOAJ
author Matteo Mozzicafreddo
Massimiliano Cuccioloni
Anna Maria Eleuteri
Mauro Angeletti
spellingShingle Matteo Mozzicafreddo
Massimiliano Cuccioloni
Anna Maria Eleuteri
Mauro Angeletti
Rapid reverse phase-HPLC assay of HMG-CoA reductase activity
Journal of Lipid Research
author_facet Matteo Mozzicafreddo
Massimiliano Cuccioloni
Anna Maria Eleuteri
Mauro Angeletti
author_sort Matteo Mozzicafreddo
title Rapid reverse phase-HPLC assay of HMG-CoA reductase activity
title_short Rapid reverse phase-HPLC assay of HMG-CoA reductase activity
title_full Rapid reverse phase-HPLC assay of HMG-CoA reductase activity
title_fullStr Rapid reverse phase-HPLC assay of HMG-CoA reductase activity
title_full_unstemmed Rapid reverse phase-HPLC assay of HMG-CoA reductase activity
title_sort rapid reverse phase-hplc assay of hmg-coa reductase activity
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 2010-08-01
description Radioisotope-based and mass spectrometry coupled to chromatographic techniques are the conventional methods for monitoring HMG-CoA reductase (HMGR) activity. Irrespective of offering adequate sensitivity, these methods are often cumbersome and time-consuming, requiring the handling of radiolabeled chemicals or elaborate ad-hoc derivatizing procedures. We propose a rapid and versatile reverse phase-HPLC method for assaying HMGR activity capable of monitoring the levels of both substrates (HMG-CoA and NADPH) and products (CoA, mevalonate, and NADP+) in a single 20 min run with no pretreatment required. The linear dynamic range was 10–26 pmol for HMG-CoA, 7–27 nmol for NADPH, 0.5–40 pmol for CoA and mevalonate, and 2–27 nmol for NADP+, and limit of detection values were 2.67 pmol, 2.77 nmol, 0.27 pmol, and 1.3 nmol, respectively.
url http://www.sciencedirect.com/science/article/pii/S0022227520370838
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AT annamariaeleuteri rapidreversephasehplcassayofhmgcoareductaseactivity
AT mauroangeletti rapidreversephasehplcassayofhmgcoareductaseactivity
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