A simple and rapid in vitro assay for identification of direct inhibitors of O 6 -methylguanine-DNA methyltransferase.
Vahid KhalajSolmaz AghaAmiriSukhen C GhoshServando Hernandez VargasMajid MomenyAli AzhdariniaPublished in: BioTechniques (2024)
O 6 -Methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that is overexpressed in certain tumors and is associated with resistance to the DNA alkylating agent temozolomide. MGMT inhibitors show potential in combating temozolomide resistance, but current assays for MGMT enzyme activity and inhibition, primarily oligonucleotide-based and fluorescent probe-based, are laborious and costly. The clinical relevance of temozolomide therapy calls for more convenient methodologies to study MGMT inhibition. Here, we extended the application of SNAP-Capture magnetic beads to develop a novel MGMT inhibition assay that demonstrated efficacy not only with known MGMT inhibitors, but also with the aldehyde dehydrogenase inhibitor, disulfiram. The assay uses standard fluorescence microscopy as a simple and reliable detection method, and is translationally applicable in drug discovery programs.
Keyphrases
- single molecule
- high throughput
- dna repair
- fluorescent probe
- circulating tumor
- drug discovery
- living cells
- cell free
- dna damage
- newly diagnosed
- loop mediated isothermal amplification
- public health
- high resolution
- stem cells
- risk assessment
- nucleic acid
- mesenchymal stem cells
- single cell
- mass spectrometry
- human health
- cell therapy
- liquid chromatography