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通过荧光共振能量转移成像技术观察质膜不同区域的Src活性。

Visualization of Src activity at different compartments of the plasma membrane by FRET imaging.

作者信息

Seong Jihye, Lu Shaoying, Ouyang Mingxing, Huang He, Zhang Jin, Frame Margaret C, Wang Yingxiao

机构信息

Neuroscience Program, Center for Biophysics and Computational Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

出版信息

Chem Biol. 2009 Jan 30;16(1):48-57. doi: 10.1016/j.chembiol.2008.11.007.

Abstract

Membrane compartments function as segregated signaling platforms for different cellular functions. It is not clear how Src is regulated at different membrane compartments. To visualize local Src activity in live cells, a FRET-based Src biosensor was targeted in or outside of lipid rafts at the plasma membrane, via acylation or prenylation modifications on targeting tags either directly fused to the biosensor or coupled to the biosensor through an inducible heterodimerization system. In response to growth factors and pervanadate, the induction of Src activity in rafts was slower and weaker, dependent on actin and possibly its mediated transportation of Src from perinuclear regions to the plasma membrane. In contrast, the induction of Src activity in nonrafts was faster and stronger, dependent on microtubules. Hence, Src activity is differentially regulated via cytoskeleton at different membrane compartments.

摘要

膜区室作为不同细胞功能的隔离信号平台发挥作用。目前尚不清楚Src在不同膜区室是如何被调控的。为了在活细胞中可视化局部Src活性,一种基于荧光共振能量转移(FRET)的Src生物传感器通过对靶向标签进行酰化或异戊二烯化修饰,被靶向定位于质膜脂筏内部或外部,这些靶向标签要么直接融合到生物传感器上,要么通过诱导性异源二聚化系统与生物传感器偶联。响应生长因子和过钒酸盐时,脂筏中Src活性的诱导较慢且较弱,这依赖于肌动蛋白以及可能由其介导的Src从核周区域向质膜的转运。相比之下,非脂筏中Src活性的诱导更快且更强,依赖于微管。因此,Src活性在不同膜区室通过细胞骨架受到差异调控。

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