Submitochondrial particles from Saccharomyces cerevisiae to screen compounds for antiprotozoal activity

Carmen Streicher, Gerlinde Wiesenberger, Thomas Rosenau, Lars Gille
2007 BMC Pharmacology  
The development of atovaquone (ATQ)-resistant plasmodia strains suggests a need of new drugs for the mitochondrial bc 1 complex as drug target in protozoa. It was the aim of the study to establish a model consisting of submitochondrial particles (SMP) from yeast (mimicking the protozoal drug target) and bovine heart for the screening of compounds. Saccharomyces cerevisiae wild-type strains (W303-1A, DBY747) were grown on YPD-media at 30°C for three days. After harvesting the cells their cell
more » ... cells their cell wall was digested by zymolyase and mitochondria were isolated. From these organelles SMP where prepared by sonication. The inhibition of the quinol:cyt c oxidoreductase activity catalyzed by the mitochondrial bc 1 complex of yeast and bovine heart SMP was measured for a nonspecies-specific inhibitor stigmatellin and for the anti-malaria drug ATQ. IC 50 values for stigmatellin in both SMP preparations confirmed its nonselectivity while ATQ inhibited the yeast complex activity about 16 times stronger than the activity of bovine heart SMP. This confirms the functionality of yeast SMP as model for protozoa. A new lead structure TMC2O demonstrated an IC 50 value of 808 μM and 112 μM in yeast and bovine heart SMP, respectively. This suggests that structural adjustments are required to increase the inhibition in yeast/protozoa. The yeast model in context with yeast strains mimicking mutated protozoa provides an efficient way to develop drugs for ATQ-resistant plasmodia strains.
doi:10.1186/1471-2210-7-s2-a56 fatcat:dzoioxfedjebxgz2237bywlzla