کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1394607 1501174 2011 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Site-directed mutagenesis provides insights into the selective binding of trityl derivatives to Plasmodium falciparum dUTPase
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آلی
پیش نمایش صفحه اول مقاله
Site-directed mutagenesis provides insights into the selective binding of trityl derivatives to Plasmodium falciparum dUTPase
چکیده انگلیسی

We have previously identified a series of triphenylmethane derivatives of deoxyuridine with antimalarial activity in vitro which selectively inhibit Plasmodium falciparum deoxyuridine triphosphate nucleotidohydrolase (PfdUTPase) compared to the human enzyme. The crystal structure of PfdUTPase in complex with one of these inhibitors suggested that the triphenylmethane derivative was selective due to a series of interactions between the trityl group and the side chains of residues Phe46, Ile117 and Lys96 located in a hydrophobic pocket distinct from the phosphate binding site. Here we show by site-directed mutagenesis that the hydrophobic nature of the trityl binding site and in particular aromatic interactions established between the inhibitor and residue Phe46 contribute significantly to the binding of uracil-based derivatives containing trityl groups in the 5′-position. Thus, changing Phe46 for alanine resulted in increased Ki values for all compounds tested. Conversely, substitution of the polar residue Lys96 for Ala results in smaller Ki values and an increase in selectivity with regard to human dUTPase. This information will aid in the design of inhibitors with improved activity against the Plasmodium enzyme.

Figure optionsDownload as PowerPoint slideHighlights
► Triphenylmethane derivatives of deoxyuridine bind selectively to Plasmodium dUTPase.
► There are specific interactions between the trityl group and Phe46, Ile117 and Lys96.
► Site-directed mutagenesis of the binding site was performed.
► Changes in the hydrophobicity of the trityl binding site modulate binding affinity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Medicinal Chemistry - Volume 46, Issue 8, August 2011, Pages 3309–3314
نویسندگان
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