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Updated: May 19, 2026

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Assay Development for High-Throughput Drug Screening Against Mycobacteria
Published on: October 25, 2024
Synthesis and evaluation of a selective fluorogenic Pup derived assay reagent for Dop, a potential drug target in
Remco Merkx1, Kristin E Burns, Paul Slobbe
1Division of Cell Biology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Chembiochem : a European Journal of Chemical Biology
|August 29, 2012
Abstract:
A litter of pups: The synthesis and in vitro evaluation of new Pup-based fluorogenic substrates for Dop, the mycobacterial depupylase, are described. A full-length Pup-amidomethylcoumarin conjugate as well as an amino-terminus-truncated analogue exhibited high sensitivity and specificity towards hydrolysis by Dop. The substrates developed here might find application as high-throughput screening assay reagents for the identification of Dop inhibitors.

