4.5 Article

Fluorescence-based microtiter plate assay for glutamate-cysteine ligase activity

Journal

ANALYTICAL BIOCHEMISTRY
Volume 318, Issue 2, Pages 175-180

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S0003-2697(03)00143-X

Keywords

glutamate-cysteine ligase; glutathione; microtiter plate; fluorescence

Funding

  1. NCI NIH HHS [1P01 CA 74184] Funding Source: Medline
  2. NIA NIH HHS [1P01 AG 01751] Funding Source: Medline
  3. NIEHS NIH HHS [P30 ES 07033, 1T32 ES 07032, 1P42 ES 04696] Funding Source: Medline

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Glutamate-cysteine ligase (GCL; also known as gamma-glutamyleysteine synthetase) is the rate-limiting enzyme in glutathione (GSH) synthesis. Traditional assays for the activity of this enzyme are based either on coupled reactions with other enzymes or on high-performance liquid chromatography (HPLC) assessment of gamma-glutamylcysteine (gamma-GC) product formation. We took advantage of the reaction of naphthalene dicarboxaldehyde (NDA) with GSH or gamma-GC to form cyclized products that are highly fluorescent. Hepa-1 cells which were designed to overexpress mouse GCL and mouse liver homogenates were used to evaluate and compare the utility of the NDA method with an assay based on monobromobimane derivatization and HPLC analysis with fluorescence detection. Excellent agreement was found between GCL activities measured by HPLC and NDA-microtiter plate analyses. This assay should be useful for high-throughput GCL activity analyses. (C) 2003 Elsevier Science (USA). All rights reserved.

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