Steverding Dietmar, Pemberton Alexander J, Royle Howard, Spackman Robert W, Rivett A Jennifer
Biomedical Research Centre, School of Medicine, Health Policy and Practice, University of East Anglia, Norwich, UK.
Planta Med. 2006 Jun;72(8):761-3. doi: 10.1055/s-2006-931600. Epub 2006 May 29.
The natural compound tyropeptin A, a new peptidyl aldehyde proteasome inhibitor, was tested for its trypanocidal activity in vitro using culture-adapted bloodstream forms of Trypanosoma brucei. The concentrations of tyropeptin A required to reduce the growth rate by 50 % and to kill all cells were 10 and 100 times lower for bloodstream-form trypanosomes than for human leukaemia HL-60 cells, respectively. Enzymatic analysis showed that the trypsin-like activity of the trypanosome proteasome and the chymotrypsin-like activity of the mammalian proteasome are particularly sensitive to inhibition by tyropeptin A. The results suggest that natural compounds targeting the trypsin-like activity of the proteasome may serve as leads for rational drug development of novel anti-trypanosomal agents.
天然化合物酪肽素A是一种新型肽基醛蛋白酶体抑制剂,利用适应培养的布氏锥虫血流形式在体外测试了其杀锥虫活性。对于血流形式的锥虫,使生长速率降低50%和杀死所有细胞所需的酪肽素A浓度分别比人白血病HL-60细胞低10倍和100倍。酶分析表明,锥虫蛋白酶体的胰蛋白酶样活性和哺乳动物蛋白酶体的糜蛋白酶样活性对酪肽素A的抑制特别敏感。结果表明,靶向蛋白酶体胰蛋白酶样活性的天然化合物可能作为新型抗锥虫药物合理开发的先导物。