Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/11216
Title: Global kinomic and phospho-proteomic analyses of the human malaria parasite Plasmodium falciparum.
Authors: Solyakov, L
Halbert, J
Alam, MM
Semblat, JP
Dorin-Semblat, D
Reininger, L
Bottrill, AR
Mistry, S
Abdi, A
Fennell, C
Holland, Z
Demarta, C
Bouza, Y
Sicard, A
Nivez, MP
Eschenlauer, S
Lama, T
Thomas, DC
Sharma, P
Agarwal, S
Kern, S
Pradel, G
Graciotti, M
Tobin, AB
Doerig, C
First Published: 2011
Citation: NAT COMMUN, 2011, 2, pp. 565-565
Abstract: The role of protein phosphorylation in the life cycle of malaria parasites is slowly emerging. Here we combine global phospho-proteomic analysis with kinome-wide reverse genetics to assess the importance of protein phosphorylation in Plasmodium falciparum asexual proliferation. We identify 1177 phosphorylation sites on 650 parasite proteins that are involved in a wide range of general cellular activities such as DNA synthesis, transcription and metabolism as well as key parasite processes such as invasion and cyto-adherence. Several parasite protein kinases are themselves phosphorylated on putative regulatory residues, including tyrosines in the activation loop of PfGSK3 and PfCLK3; we show that phosphorylation of PfCLK3 Y526 is essential for full kinase activity. A kinome-wide reverse genetics strategy identified 36 parasite kinases as likely essential for erythrocytic schizogony. These studies not only reveal processes that are regulated by protein phosphorylation, but also define potential anti-malarial drug targets within the parasite kinome.
DOI Link: 10.1038/ncomms1558
eISSN: 2041-1723
Links: http://hdl.handle.net/2381/11216
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Cell Physiology and Pharmacology

Files in This Item:
There are no files associated with this item.


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.