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Beilstein J Org Chem. 2013;9:89-96. doi: 10.3762/bjoc.9.12. Epub 2013 Jan 15.

An improved synthesis of a fluorophosphonate-polyethylene glycol-biotin probe and its use against competitive substrates.

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  • 1Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109-1065, USA ; Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI 48109-1065, USA.

Abstract

The fluorophosphonate (FP) moiety attached to a biotin tag is a prototype chemical probe used to quantitatively analyze and enrich active serine hydrolases in complex proteomes in an approach called activity-based protein profiling (ABPP). In this study we have designed a novel synthetic route to a known FP probe linked by polyethylene glycol to a biotin tag (FP-PEG-biotin). Our route markedly increases the efficiency of the probe synthesis and overcomes several problems of a prior synthesis. As a proof of principle, FP-PEG-biotin was evaluated against isolated protein mixtures and different rat-tissue homogenates, showing its ability to specifically target serine hydrolases. We also assessed the ability of FP-PEG-biotin to compete with substrates that have high enzyme turnover rates. The reduced protein-band intensities resulting in these competition studies demonstrate a new application of FP-based probes seldom explored before.

KEYWORDS:

biotin; fluorophosphonate; high turnover rate; reversible substrate

PMID:
23400700
[PubMed]
PMCID:
PMC3566859
Free PMC Article
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