IRSp53: crossing the road of membrane and actin dynamics in the formation of membrane protrusions

被引:198
作者
Scita, Giorgio [1 ,2 ]
Confalonieri, Stefano [1 ]
Lappalainen, Pekka [3 ]
Suetsugu, Shiro [4 ]
机构
[1] IFOM FIRC Inst Mol Oncol Fdn, I-20139 Milan, Italy
[2] Univ Milan, Sch Med, I-20122 Milan, Italy
[3] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[4] Univ Tokyo, Lab Membrane & Cytoskeleton Dynam, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
关键词
D O I
10.1016/j.tcb.2007.12.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A tight spatiotemporal coordination of the machineries controlling membrane bending and trafficking, and actin dynamics is crucial for the generation of cellular protrusions. Proteins that are simultaneously capable of regulating actin dynamics and sensing or inducing membrane curvature are predicted to have a prominent role. A prototypical example of this type of proteins is the insulin receptor tyrosine kinase substrate of 53 kDa, the founding member of a recently discovered family of proteins, including missing-in-metastasis and ABBA (actin-bundling protein with BAIAP2 homology). Structural, biochemical and cell biological experiments support the unique role of this family as transducers of signalling, linking the protruding membrane to the underlying actin cytoskeleton.
引用
收藏
页码:52 / 60
页数:9
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