Many infectious pathogens have a complex life cycle alternating between free-living creature and cell-enclosed parasite. A thorough analysis of the proteins that help them undergo this lifestyle change can prove very useful for drug or vaccine development
However, separating the parasites from their host cell for detailed study has been extremely difficult to date.
Research leader Toni Aebischer has revealed that he and his colleagues worked around this problem by designing special special fluorescent Leishmania mexicana, one of the many Leishmaniases parasites.
Writing about their study in the journal Molecular and Cellular Proteomics, the researchers have revealed that they passed infected cells through a machine that can separate cell components based on how much they glow.
They say that the new approach allowed them to separated the Leishmania parasites with only about two per cent contamination, far better than current methods.
The team later successfully identified 509 proteins in the parasites, 34 of which were more prominent in parasites than free -living Leishmania.
The study also revealed many characteristics of the organisms, such as a high presence of fatty acid degrading enzymes, which highlights adaptation to intracellularly available energy sources.
Aebischer and his colleagues believe that the identified proteins can provide a good data set for continued selection of drug targets.
According to the researchers, the success of their approach should make it a good resource for other cellular parasites like malaria.