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MglA 在粘细菌滑动运动中的作用及其定位研究

Localization of MglA, an essential gliding motility protein in Myxococcus xanthus.

机构信息

Department of Microbiology, Molecular Biology, and Biochemistry, University of Idaho, Moscow, Idaho, USA.

出版信息

Cytoskeleton (Hoboken). 2010 May;67(5):322-37. doi: 10.1002/cm.20447.

Abstract

MglA, a 22-kDa protein related to monomeric GTPases, is required for the normal operation of the A (Adventurous) and S (Social) motility and for multicellular development of Myxococcus xanthus. To determine how MglA controls A- and S-motility, MglA was assayed biochemically and its cellular location was determined. His-tagged MglA hydrolyzed GTP slowly in vitro at a rate nearly identical to that of Ras showing that MglA has GTPase activity. Immunofluorescence microscopy of fixed cells from liquid showed that MglA was associated with helical track similar to the MreB spiral that spanned the length of the cell. The distribution pattern of MglA depended on the type of surface from which cells were harvested. In cells gliding on 1.5% (w/v) agar, the helical pattern gave way to punctate clusters of MglA-Yfp at the poles and along the long axis (lateral clusters). The lateral clusters emerged near the leading pole as the cell advanced coincident with a decrease in the intensity of the MglA-Yfp cluster at the leading pole. Newly formed lateral clusters remained fixed with regard to the substratum as the cell moved forward, similar to focal adhesion complexes described for AglZ, a protein partner of MglA. Lateral clusters did not form in cells gliding in methylcellulose, a polymer that stimulates S-motility at low cell density; rather MglA-Yfp was diffuse in the cytoplasm and more concentrated at the poles. The results suggest that conditions that favor S-motility prevent the formation of lateral clusters of MglA, which are associated with A-motility functions.

摘要

MglA 是一种 22kDa 的蛋白,与单体 GTP 酶有关,是 A(冒险型)和 S(社交型)运动以及粘球菌多细胞发育正常运行所必需的。为了确定 MglA 如何控制 A- 和 S- 运动,我们对 MglA 进行了生化分析,并确定了其细胞位置。His 标记的 MglA 在体外缓慢水解 GTP,其速率与 Ras 几乎相同,表明 MglA 具有 GTP 酶活性。固定细胞的免疫荧光显微镜显示,MglA 与螺旋轨道相关,类似于跨越细胞长度的 MreB 螺旋。MglA 的分布模式取决于收获细胞的表面类型。在在 1.5%(w/v)琼脂上滑行的细胞中,螺旋模式让位于极点和长轴(侧群)上的 MglA-Yfp 点状簇。随着细胞的前进,侧群在前沿极点附近出现,同时前沿极点处的 MglA-Yfp 簇强度降低。新形成的侧群随着细胞向前移动相对于基质保持固定,类似于 AglZ(MglA 的蛋白伴侣)的粘着斑复合物。在低细胞密度下刺激 S-运动的甲基纤维素中滑行的细胞中不会形成侧群;相反,MglA-Yfp 在细胞质中弥散,在极点处更集中。结果表明,有利于 S-运动的条件会阻止与 A-运动功能相关的 MglA 侧群的形成。

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