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Issue 3, 2008
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Selective and diagnostic labelling of serine hydrolases with reactive phosphonate inhibitors

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Abstract

Reactive phosphonates are important probes to target the active site of serine hydrolases, one of the largest and most diverse family of enzymes. Developing such inhibitory probes is of special importance in activity based protein profiling, a strategy that is increasingly used to gain information about a certain class of enzymes in complex proteosomes. Therefore, gaining detailed information about these inhibition events on the individual protein level is important since it affords information that can be used to fine-tune the probe for a specific task. Here, we report a novel and versatile synthesis protocol to access a variety of functionalised p-nitrophenyl phosphonate (PNPP) inhibitors from a common azide functionalised precursor using click chemistry. The obtained PNPPs were successfully used to covalently label serine hydrolases in their active sites with molecular tags. Furthermore, a model study is described in which we developed straightforward protocols that can be used to study protein inhibition events. Kinetic studies using UV–Vis and fluorescence spectroscopy techniques revealed that these PNPPs possess different inhibition rates for various proteins and were shown to be suitable probes to discriminate between various lipases. Additionally, we demonstrate that PNPPs are highly selective for serine hydrolases, making these probes very interesting as diagnostic or affinity probes for studying proteins in complex proteosomes.

Graphical abstract: Selective and diagnostic labelling of serine hydrolases with reactive phosphonate inhibitors

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Publication details

The article was received on 09 Nov 2007, accepted on 29 Nov 2007 and first published on 17 Dec 2007


Article type: Paper
DOI: 10.1039/B717345H
Citation: Org. Biomol. Chem., 2008,6, 523-531
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    Selective and diagnostic labelling of serine hydrolases with reactive phosphonate inhibitors

    H. P. Dijkstra, H. Sprong, B. N. H. Aerts, C. A. Kruithof, M. R. Egmond and R. J. M. Klein Gebbink, Org. Biomol. Chem., 2008, 6, 523
    DOI: 10.1039/B717345H

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