Abstract:
:Chagas' disease, caused by the protozoan Trypanosoma cruzi, is endemic in Latin America, which current treatment presents variable efficacy and serious side effects. A previous screening of naphthoquinone derivatives pointed to the naphthoimidazoles N1, N2 and N3 as the most active compounds against T. cruzi. In this study, a proteomic approach was employed to identify proteins involved in the N1, N2 and N3 trypanocidal activity. In epimastigotes, the naphthoimidazoles are involved in multiple mechanisms: (a) redox metabolism; (b) energy production; (c) ergosterol biosynthesis; (d) cytoskeleton assembly; (e) protein metabolism and biosynthesis; and (f) chaperones modulation. They induce an imbalance in crucial pathways of the parasite, leading to the loss of metabolic homeostasis and T. cruzi death.
journal_name
J Proteomicsjournal_title
Journal of proteomicsauthors
Menna-Barreto RF,Beghini DG,Ferreira AT,Pinto AV,De Castro SL,Perales Jdoi
10.1016/j.jprot.2010.07.002subject
Has Abstractpub_date
2010-11-10 00:00:00pages
2306-15issue
12eissn
1874-3919issn
1876-7737pii
S1874-3919(10)00206-Xjournal_volume
73pub_type
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