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Gadakh, Bharat; Vondenhoff, Gaston; Pang, Luping; Nautiyal, Manesh; De Graef, Steff; Strelkov, Sergei V.; Weeks, Stephen D.; Van Aerschot, Arthur
Bioorganic & medicinal chemistry, 09/2020, Letnik: 28, Številka: 17Journal Article
Display omitted •Total synthesis of albomycin core scaffold targeting serRS was accomplished.•Additional aspartyl- and isoleucyl-congeners were elaborated.•Aspartyl analogue strongly inhibiting aspRS in contrast to isoleucyl analogue.•3D-Structural analysis of the albomycin core scaffold-serRS interactions.•Co-crystal structure of the aspartyl analogue and its aspRS target. Despite of proven efficacy and well tolerability, albomycin is not used clinically due to scarcity of material. Several attempts have been made to increase the production of albomycin by chemical or biochemical methods. In the current study, we have synthesized the active moiety of albomycin δ1 and investigated its binding mode to its molecular target seryl-trna synthetase (SerRS). In addition, isoleucyl and aspartyl congeners were prepared to investigate whether the albomycin scaffold can be extrapolated to target other aminoacyl-tRNA synthetases (aaRSs) from both class I and class II aaRSs, respectively. The synthesized analogues were evaluated for their ability to inhibit the corresponding aaRSs by an in vitro aminoacylation experiment using purified enzymes. It was observed that the diastereomer having the 5′S, 6′R-configuration (nucleoside numbering) as observed in the crystal structure, exhibits excellent inhibitory activity in contrast to poor activity of its companion 5′R,6′S-diasteromer obtained as byproduct during synthesis. Moreover, the albomycin core scaffold seems well tolerated for class II aaRSs inhibition compared with class I aaRSs. To understand this bias, we studied X-ray crystal structures of SerRS in complex with the albomycin δ1 core structure 14a, and AspRS in complex with compound 16a. Structural analysis clearly showed that diastereomer selectivity is attributed to the steric restraints of the active site of SerRS and AspRS.
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