Key result
A novel fluorogenic peptide substrate P08 enabled the development of a biochemical assay that identified compound 3 as an effective EV71 3C protease inhibitor (IC50 = 1.89 μM).
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The development of a novel fluorogenic peptide substrate and a robust biochemical assay provides an effective platform for discovering anti-EV71 drugs targeting the 3C protease.
Enterovirus 71 (EV71), a primary pathogen of hand, foot, and mouth disease (HFMD), affects primarily infants and children. Currently, there are no effective drugs against HFMD. EV71 3C protease performs multiple tasks in the viral replication, which makes it an ideal antiviral target. We synthesized a small set of fluorogenic model peptides derived from cleavage sites of EV71 polyprotein and examined their efficiencies of cleavage by EV71 3C protease. The novel peptide P08 [(2-(N-methylamino)benzoyl) (NMA)-IEALFQGPPK(DNP)FR] was determined to be the most efficiently cleaved by EV71 3C protease, with a kinetic constant kcat/Km of 11.8 ± 0.82 mM(-1) min(-1). Compared with literature reports, P08 gave significant improvement in the signal/background ratio, which makes it an attractive substrate for assay development. A Molecular dynamics simulation study elaborated the interactions between substrate P08 and EV71 3C protease. Arg39, which is located at the bottom of the S2 pocket of EV71 3C protease, may participate in the proteolysis process of substrates. With an aim to evaluate EV71 3C protease inhibitors, a reliable and robust biochemical assay with a Z' factor of 0.87 ± 0.05 was developed. A novel compound (compound 3) (50% inhibitory concentration [IC50] = 1.89 ± 0.25 μM) was discovered using this assay, which effectively suppressed the proliferation of EV 71 (strain Fuyang) in rhabdomyosarcoma (RD) cells with a highly selective index (50% effective concentration [EC50] = 4.54 ± 0.51 μM; 50% cytotoxic concentration [CC50] > 100 μM). This fast and efficient assay for lead discovery and optimization provides an ideal platform for anti-EV71 drug development targeting 3C protease.
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Shang et al. (2014) studied Enterovirus 71 (EV71) infection / Hand, foot, and mouth disease. Fluorogenic model peptide substrate P08 and Compound 3 was evaluated on Cleavage efficiency and inhibitory concentration (IC50). A novel fluorogenic peptide substrate P08 enabled the development of a biochemical assay that identified compound 3 as an effective EV71 3C protease inhibitor (IC50 = 1.89 μM).
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