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使用绿色荧光蛋白(GFP)与肌动蛋白结合域之间的融合蛋白来可视化瞬时丝状肌动蛋白结构。

Use of a fusion protein between GFP and an actin-binding domain to visualize transient filamentous-actin structures.

作者信息

Pang K M, Lee E, Knecht D A

机构信息

Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut 06269, USA.

出版信息

Curr Biol. 1998 Mar 26;8(7):405-8. doi: 10.1016/s0960-9822(98)70159-9.

Abstract

Many important processes in eukaryotic cells involve changes in the quantity, location and the organization of actin filaments [1] [2] [3]. We have been able to visualize these changes in live cells using a fusion protein (GFP-ABD) comprising the green fluorescent protein (GFP) of Aequorea victoria and the 25 kDa highly conserved actin-binding domain (ABD) from the amino terminus of the actin cross-linking protein ABP-120 [4]. In live cells of the soil amoeba Dictyostelium that were expressing GFP-ABD, the three-dimensional architecture of the actin cortex was clearly visualized. The pattern of GFP-ABD fluorescence in these cells coincided with that of rhodamine-phalloidin, indicating that GFP-ABD specifically binds filamentous (F) actin. On the ventral surface of non-polarized vegetative cells, a broad ring of F actin periodically assembled and contracted, whereas in polarized cells there were transient punctate F-actin structures; cells cycled between the polarized and non-polarized morphologies. During the formation of pseudopods, an increase in fluorescence intensity coincided with the initial outward deformation of the membrane. This is consistent with the models of pseudopod extension that predict an increase in the local density of actin filaments. In conclusion, GFP-ABD specifically binds F actin and allows the visualization of F-actin dynamics and cellular behavior simultaneously.

摘要

真核细胞中的许多重要过程都涉及肌动蛋白丝的数量、位置和组织的变化[1][2][3]。我们能够使用一种融合蛋白(GFP-ABD)在活细胞中观察到这些变化,该融合蛋白由维多利亚水母的绿色荧光蛋白(GFP)和肌动蛋白交联蛋白ABP-120氨基末端的25 kDa高度保守的肌动蛋白结合结构域(ABD)组成[4]。在表达GFP-ABD的土壤变形虫盘基网柄菌的活细胞中,肌动蛋白皮质的三维结构清晰可见。这些细胞中GFP-ABD荧光的模式与罗丹明-鬼笔环肽的模式一致,表明GFP-ABD特异性结合丝状(F)肌动蛋白。在非极化营养细胞的腹表面,一圈宽阔的F肌动蛋白周期性地组装和收缩,而在极化细胞中有短暂的点状F-肌动蛋白结构;细胞在极化和非极化形态之间循环。在伪足形成过程中,荧光强度的增加与膜的初始向外变形同时发生。这与预测肌动蛋白丝局部密度增加的伪足延伸模型一致。总之,GFP-ABD特异性结合F肌动蛋白,并允许同时观察F-肌动蛋白动力学和细胞行为。

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