| Literature DB >> 25875590 |
Qiang Fu1, Jun Tang1, Meng Cui2, Zhong Zheng3, Zhiqiang Liu3, Shuying Liu3.
Abstract
The continuous enzymatic assay based on ESI-MS was developed to real-time monitoring of enzymatic reactions of acetylcholinesterase (AChE). The changes of product concentrations were continuously measured. Calibration curves were established for quantitative calculation. By this method, the Michaelis constant (Km) of acetylcholinesterase was determined to be 70.60±0.93μM and Huperzine A as an effective inhibitor of acetylcholinesterase displayed a mixed inhibition with competitive and noncompetitive inhibition behaviors. The half maximal inhibitory concentration (IC50) and inhibition constant (Ki) value of Huperzine A were also calculated as 48.51±1.16nM and 26.73±0.27nM, respectively. This method provides the rapid and accurate ways to monitor enzyme reactions.Entities:
Keywords: Continuous enzymatic assay; ESI-MS; Half maximal inhibitory concentration (IC50); Inhibition constant (Ki); Michaelis constant (Km)
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Year: 2015 PMID: 25875590 DOI: 10.1016/j.jchromb.2015.03.022
Source DB: PubMed Journal: J Chromatogr B Analyt Technol Biomed Life Sci ISSN: 1570-0232 Impact factor: 3.205