| Literature DB >> 35881342 |
Margarida Ressurreição1, Robert William Moon1, David Andrew Baker1, Christiaan van Ooij2.
Abstract
Synchronisation of Plasmodium cultures is essential to investigate the complexities of time-dependent events associated with the asexual blood stage of the malaria parasite life cycle. Here we describe a procedure using ML10, a highly specific inhibitor of the parasite cyclic GMP-dependent protein kinase (PKG), to attain high synchronicity of Plasmodium falciparum and P. knowlesi asexual blood-stage cultures and to obtain high levels of arrested mature schizonts as well as viable released merozoites. Additionally, we describe how to use ML10 to improve the transfection efficiency of P. falciparum parasites and also how to derive the half maximal effective concentration (EC50) of ML10 in other P. falciparum laboratory lines and clinical isolates.Entities:
Keywords: Egress; Exoneme; Invasion; ML10 inhibitor; Merozoite; Microneme; PKG; PVM; Protein kinase; Schizont; Synchronization
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Year: 2022 PMID: 35881342 DOI: 10.1007/978-1-0716-2189-9_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745