In Silico Identification and in Vitro Activity of Novel Natural Inhibitors of Trypanosoma brucei Glyceraldehyde-3-phosphate-dehydrogenase

被引:18
|
作者
Herrmann, Fabian C. [1 ]
Lenz, Mairin [1 ]
Jose, Joachim [2 ]
Kaiser, Marcel [3 ,4 ]
Brun, Reto [3 ,4 ]
Schmidt, Thomas J. [1 ]
机构
[1] Univ Munster, IPBP, D-48149 Munster, Germany
[2] Univ Munster, Inst Pharmazeut & Med Chem, D-48149 Munster, Germany
[3] Swiss Trop & Publ Hlth Inst Swiss TPH, CH-4002 Basel, Switzerland
[4] Univ Basel, CH-4003 Basel, Switzerland
关键词
Trypanosoma brucei; human African trypanosomiasis; glyceraldehyde-3-phosphate dehydrogenase inhibitor; natural product; in silico screening; in vitro antitrypanosomal activity; PROTOZOAN NEGLECTED DISEASES; BLOOD-STREAM FORM; ANTIPROTOZOAL ACTIVITY; SECONDARY METABOLITES; DEHYDROGENASE; LEADS; CONSTITUENT; PREDICTION; ENZYMES; PLANTS;
D O I
10.3390/molecules200916154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As part of our ongoing efforts to identify natural products with activity against pathogens causing neglected tropical diseases, we are currently performing an extensive screening of natural product (NP) databases against a multitude of protozoan parasite proteins. Within this project, we screened a database of NPs from a commercial supplier, AnalytiCon Discovery (Potsdam, Germany), against Trypanosoma brucei glyceraldehyde-3-phosphate dehydrogenase (TbGAPDH), a glycolytic enzyme whose inhibition deprives the parasite of energy supply. NPs acting as potential inhibitors of the mentioned enzyme were identified using a pharmacophore-based virtual screening and subsequent docking of the identified hits into the active site of interest. In a set of 700 structures chosen for the screening, 13 (1.9%) were predicted to possess significant affinity towards the enzyme and were therefore tested in an in vitro enzyme assay using recombinant TbGAPDH. Nine of these in silico hits (69%) showed significant inhibitory activity at 50 mu M, of which two geranylated benzophenone derivatives proved to be particularly active with IC50 values below 10 mu M. These compounds also showed moderate in vitro activity against T. brucei rhodesiense and may thus represent interesting starting points for further optimization.
引用
收藏
页码:16154 / 16169
页数:16
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