Targeted Proteomic Dissection of Toxoplasma Cytoskeleton Sub-Compartments using MORN1

被引:38
作者
Lorestani, Alexander [1 ]
Ivey, F. Douglas [1 ]
Thirugnanam, Sivasakthivel [1 ]
Busby, Michele A. [1 ]
Marth, Gabor T. [1 ]
Cheeseman, Iain M. [2 ,3 ]
Gubbels, Marc-Jan [1 ]
机构
[1] Boston Coll, Dept Biol, Chestnut Hill, MA 02467 USA
[2] MIT, Dept Biol, Cambridge, MA USA
[3] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
基金
美国国家卫生研究院;
关键词
Apicomplexa; Toxoplasma; MORN1; basal complex; cytoskeleton; motility; ACTIN DEPOLYMERIZING FACTOR; HOST-CELL INVASION; SEQUESTER G-ACTIN; XIV MYOSIN; GONDII; PROTEIN; MOTILITY; IDENTIFICATION; PLASMODIUM; PARASITES;
D O I
10.1002/cm.21077
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The basal complex in Toxoplasma functions as the contractile ring in the cell division process. Basal complex contraction tapers the daughter cytoskeleton toward the basal end and is required for daughter segregation. We have previously shown that the protein MORN1 is essential for basal complex assembly and likely acts as a scaffolding protein. To further our understanding of the basal complex, we combined subcellular fractionation with an affinity purification of the MORN1 complex and identified its protein composition. We identified two new components of the basal complex, one of which uniquely associated with the basal complex in mature parasites, the first of its kind. In addition, we identified several other novel cytoskeleton proteins with different spatiotemporal dynamics throughout cell division. Since many of these proteins are unique to Apicomplexa this study significantly contributes to the annotation of their unique cytoskeleton. Furthermore, we show that G-actin binding protein TgCAP is localized at the apical cap region in intracellular parasites, but quickly redistributes to a cytoplasmic localization pattern upon egress. (C) 2012 Wiley Periodicals, Inc
引用
收藏
页码:1069 / 1085
页数:17
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