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作为囊泡运输协调因子的Rab小GTP酶

Rab GTPases as coordinators of vesicle traffic.

作者信息

Stenmark Harald

机构信息

Department of Biochemistry, Institute for Cancer Research, The Norwegian Radium Hospital, University of Oslo, Montebello, N-0310 Oslo, Norway.

出版信息

Nat Rev Mol Cell Biol. 2009 Aug;10(8):513-25. doi: 10.1038/nrm2728. Epub 2009 Jul 15.

Abstract

Membrane trafficking between organelles by vesiculotubular carriers is fundamental to the existence of eukaryotic cells. Central in ensuring that cargoes are delivered to their correct destinations are the Rab GTPases, a large family of small GTPases that control membrane identity and vesicle budding, uncoating, motility and fusion through the recruitment of effector proteins, such as sorting adaptors, tethering factors, kinases, phosphatases and motors. Crosstalk between multiple Rab GTPases through shared effectors, or through effectors that recruit selective Rab activators, ensures the spatiotemporal regulation of vesicle traffic. Functional impairments of Rab pathways are associated with diseases, such as immunodeficiencies, cancer and neurological disorders.

摘要

通过囊泡管状载体在细胞器之间进行的膜运输对于真核细胞的生存至关重要。Rab GTPases在确保货物被运送到正确目的地方面起着核心作用,Rab GTPases是一类大型的小GTPases,通过招募效应蛋白(如分选衔接蛋白、拴系因子、激酶、磷酸酶和马达蛋白)来控制膜的特性以及囊泡的出芽、去包被、运动和融合。多个Rab GTPases之间通过共享效应蛋白,或通过招募选择性Rab激活剂的效应蛋白进行串扰,从而确保囊泡运输的时空调节。Rab途径的功能障碍与免疫缺陷、癌症和神经疾病等疾病相关。

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