A label-free MALDI TOF MS-based method for studying the kinetics and inhibitor screening of the Alzheimer's disease drug target β-secretase
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
CEITEC 2020 (LQ1601)
Ministry of Education, Youth and Sports of the Czech Republic
GA16-06106S
Grantová Agentura České Republiky
MUNI/G/0974/2016
Grant Agency of Masaryk University
PubMed
30218128
DOI
10.1007/s00216-018-1354-6
PII: 10.1007/s00216-018-1354-6
Knihovny.cz E-resources
- Keywords
- Enzyme assay, High throughput, Inhibition, MALDI TOF MS, β-Secretase,
- MeSH
- Alzheimer Disease enzymology MeSH
- Amino Acids antagonists & inhibitors MeSH
- HEK293 Cells MeSH
- Heterocyclic Compounds, 2-Ring pharmacology MeSH
- Kinetics MeSH
- Picolinic Acids pharmacology MeSH
- Humans MeSH
- Drug Evaluation, Preclinical methods MeSH
- Pyrimidinones pharmacology MeSH
- Amyloid Precursor Protein Secretases antagonists & inhibitors metabolism MeSH
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Amino Acids MeSH
- donetidine MeSH Browser
- Heterocyclic Compounds, 2-Ring MeSH
- Picolinic Acids MeSH
- N-(3-(2-amino-4a,5,7,7a-tetrahydro-4H-furo(3,4-d)(1,3)thiazin-7a-yl)-4-fluorophenyl)-5-fluoropicolinamide MeSH Browser
- Pyrimidinones MeSH
- Amyloid Precursor Protein Secretases MeSH
- statine MeSH Browser
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) is a well-established method with a unique set of qualities including sensitivity, minute sample consumption, and label-free detection, all of which are highly desired in enzyme assays. On the other hand, the application of MALDI TOF MS is usually limited by high concentrations of MS-incompatible compounds in the reaction mixture such as salts or organic solvents. Here, we introduce kinetic and inhibition studies of β-secretase (BACE1), a key enzyme of the progression of Alzheimer's disease. Compatibility of the enzyme assay with MALDI TOF MS was achieved, providing both a complex protocol including a desalting step designed for rigorous kinetic studies and a simple mix-and-measure protocol designed for high-throughput inhibitor screening. In comparison with fluorescent or colorimetric assays, MALDI TOF MS represents a sensitive, fast, and label-free technique with minimal sample preparation. In contrast to other MS-based methodological approaches typically used in drug discovery processes, such as a direct injection MS or MS-coupled liquid chromatography or capillary electrophoresis, MALDI TOF MS enables direct analysis and is a highly suitable approach for high-throughput screening. The method's applicability is strongly supported by the high correlation of the acquired kinetic and inhibition parameters with data from the literature as well as from our previous research. Graphical abstract ᅟ.
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