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Methyltransferase-Glo: a universal, bioluminescent and homogenous assay for monitoring all classes of methyltransferases
- Source :
- Epigenomics. 8(3)
- Publication Year :
- 2016
-
Abstract
- Aim: To develop a homogenous, nonradioactive, antibody-free and universal assay for diverse families of methyltransferases and monitor the activity of these enzymes in a high-throughput format. Materials & methods: The assay conditions are optimized for monitoring the enzymatic activity of a broad range of methyltransferases regardless of the chemical structure or nature of the enzyme substrate in a low- and high-throughput-formatted protocols. The assay detects S-adenosyl-l-homocysteine, the universal reaction products of all methyltransferases. Results: We demonstrate the utility of using this protocol to determine the activity of DNA, protein methyltransferases and also to determine kinetic parameters of several inhibitors using purified enzymes. The assay is sensitive (20–30 nM of S-adenosyl-l-homocysteine) and robust. Conclusion: The methyltransferase Glo is nonradioactive, antibody-free and homogenous, universal assay to determine enzyme activity of diverse families of methyltransferases. The assay is formatted to meet the requirements of high-throughput screening in drug discovery programs searching for modulators of methyltransferases.
- Subjects :
- 0301 basic medicine
Cancer Research
Methyltransferase
Sensitivity and Specificity
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Genetics
Bioluminescence
Epigenetics
Enzyme Inhibitors
chemistry.chemical_classification
biology
Substrate (chemistry)
Methylation
Methyltransferases
Molecular biology
S-Adenosylhomocysteine
Enzyme assay
High-Throughput Screening Assays
030104 developmental biology
Enzyme
chemistry
Biochemistry
030220 oncology & carcinogenesis
Luminescent Measurements
biology.protein
DNA
Subjects
Details
- ISSN :
- 1750192X
- Volume :
- 8
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Epigenomics
- Accession number :
- edsair.doi.dedup.....86ffe365a6488a97f2eb4938c6f3979d