Kawasaki Masato, Nakayama Kazuhisa, Wakatsuki Soichi
Structural Biology Research Center, Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization (KEK), Tsukuba, Ibaraki 305-0801, Japan.
Curr Opin Struct Biol. 2005 Dec;15(6):681-9. doi: 10.1016/j.sbi.2005.10.015. Epub 2005 Nov 9.
In their GTP-bound form, Arf and Rab family GTPases associate with distinct organelle membranes, to which they recruit specific sets of effector proteins that regulate vesicular transport. The Arf GTPases are involved in the formation of coated carrier vesicles by recruiting coat proteins. On the other hand, the Rab GTPases are involved in the tethering, docking and fusion of transport vesicles with target organelles, acting in concert with the tethering and fusion machineries. Recent structural studies of the Arf1-GGA and Rab5-Rabaptin-5 complexes, as well as other effector structures in complex with the Arf and Rab GTPases, have shed light on the mechanisms underlying the GTP-dependent membrane recruitment of these effector proteins.
在其结合GTP的形式下,Arf和Rab家族的GTP酶与不同的细胞器膜结合,它们在这些膜上招募特定的效应蛋白组,以调节囊泡运输。Arf GTP酶通过招募包被蛋白参与有被载体囊泡的形成。另一方面,Rab GTP酶参与运输囊泡与靶细胞器的拴系、对接和融合,并与拴系和融合机制协同作用。最近对Arf1-GGA和Rab5-Rabaptin-5复合物以及与Arf和Rab GTP酶形成复合物的其他效应器结构的结构研究,揭示了这些效应蛋白依赖GTP的膜招募机制。