Gaskins Elizabeth, Gilk Stacey, DeVore Nicolette, Mann Tara, Ward Gary, Beckers Con
Department of Cell and Developmental Biology, University of North Carolina at Chapel Hill, 108 Taylor Hall, CB# 7090, Chapel Hill, NC 27599, USA.
J Cell Biol. 2004 May 10;165(3):383-93. doi: 10.1083/jcb.200311137. Epub 2004 May 3.
Apicomplexan parasites exhibit a unique form of substrate-dependent motility, gliding motility, which is essential during their invasion of host cells and during their spread between host cells. This process is dependent on actin filaments and myosin that are both located between the plasma membrane and two underlying membranes of the inner membrane complex. We have identified a protein complex in the apicomplexan parasite Toxoplasma gondii that contains the class XIV myosin required for gliding motility, TgMyoA, its associated light chain, TgMLC1, and two novel proteins, TgGAP45 and TgGAP50. We have localized this complex to the inner membrane complex of Toxoplasma, where it is anchored in the membrane by TgGAP50, an integral membrane glycoprotein. Assembly of the protein complex is spatially controlled and occurs in two stages. These results provide the first molecular description of an integral membrane protein as a specific receptor for a myosin motor, and further our understanding of the motile apparatus underlying gliding motility in apicomplexan parasites.
顶复门寄生虫表现出一种独特的依赖底物的运动形式,即滑行运动,这在它们侵入宿主细胞以及在宿主细胞间传播的过程中至关重要。这个过程依赖于肌动蛋白丝和肌球蛋白,它们都位于质膜和内膜复合体的两层内膜之间。我们在顶复门寄生虫刚地弓形虫中鉴定出一种蛋白质复合体,它包含滑行运动所需的第十四类肌球蛋白TgMyoA、其相关轻链TgMLC1以及两种新蛋白TgGAP45和TgGAP50。我们已将该复合体定位到弓形虫的内膜复合体上,在那里它通过一种整合膜糖蛋白TgGAP50锚定在膜上。蛋白质复合体的组装受到空间控制,分两个阶段进行。这些结果首次对一种整合膜蛋白作为肌球蛋白马达的特异性受体进行了分子描述,并进一步加深了我们对顶复门寄生虫滑行运动背后运动装置的理解。