Abstract
A pilot study was performed for the development of a method to screen compound libraries using an electrospray mass spectrometer interfaced with liquid chromatography (LC). The mixture of compounds was obtained by combining low-molecular weight inhibitors of carboxypeptidase A (CPA), a representative zinc-containing proteolytic enzyme. After the incubation of the mixture with CPA, the enzyme-bound compounds were separated by size exclusion chromatography (SEC) from unbound compounds. The separation of compounds was affected by LC. Three compounds were identified, which represent the tight binding inhibitors of the library. These compounds were quantitated using an automatic switching valve to avoid the interference of buffer salts with the detection of analytes. The quantitated amounts of the compounds were found to be in good accordance with the K values. © 2005 The Society for Biomolecular Screening.
Author supplied keywords
Cite
CITATION STYLE
Mathur, S., Park, J. D., Kim, D. H., & Hartmann, R. W. (2005). A method for screening enzyme inhibitors using size exclusion chromatography and ESI-LC-MS/MS. Journal of Biomolecular Screening, 10(1), 30–35. https://doi.org/10.1177/1087057104270270
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.