کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2829766 | 1570652 | 2013 | 10 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: The effect of fusidic acid on Plasmodium falciparum elongation factor G (EF-G) The effect of fusidic acid on Plasmodium falciparum elongation factor G (EF-G)](/preview/png/2829766.png)
• Biochemical characterization of P. falciparum mitochondrial and apicoplast EF-Gs.
• Organellar EF-Gs have differential sensitivity to the antibiotic fusidic acid (FA).
• A GVG motif in the switch I region of mitochondrial EF-G reduces sensitivity to FA.
• Thiostrepton promotes locking of mitochondrial EF-G·GDP to 70S ribosome.
Inhibition of growth of the malaria parasite Plasmodium falciparum by known translation-inhibitory antibiotics has generated interest in understanding their action on the translation apparatus of the two genome containing organelles of the malaria parasite: the mitochondrion and the relic plastid (apicoplast). We report GTPase activity of recombinant EF-G proteins that are targeted to the organelles and further use these to test the effect of the EF-G inhibitor fusidic acid (FA) on the factor–ribosome interface. Our results monitoring locking of EF-G·GDP onto surrogate Escherichia coli ribosomes as well as multi-turnover GTP hydrolysis by the factor indicate that FA has a greater effect on apicoplast EF-G compared to the mitochondrial counterpart. Deletion of a three amino acid (GVG) sequence in the switch I loop that is conserved in proteins of the mitochondrial EF-G1 family and the Plasmodium mitochondrial factor, but is absent in apicoplast EF-G, demonstrated that this motif contributes to differential inhibition of the two EF-Gs by FA. Additionally, the drug thiostrepton, that is known to target the apicoplast and proteasome, enhanced retention of only mitochondrial EF-G on ribosomes providing support for the reported effect of the drug on parasite mitochondrial translation.
Fusidic acid has a more pronounced effect on apicoplast EF-G compared to the mitochondrial factor partly attributable to a GVG sequence in the latter's switch I.Figure optionsDownload high-quality image (113 K)Download as PowerPoint slide
Journal: Molecular and Biochemical Parasitology - Volume 192, Issues 1–2, November–December 2013, Pages 39–48