Ras assemblies and signaling at the membrane

被引:24
|
作者
Nussinov, Ruth [1 ,2 ]
Tsai, Chung-Jung [1 ]
Jang, Hyunbum [1 ]
机构
[1] NCI, Computat Struct Biol Sect, Frederick Natl Lab Canc Res, Frederick, MD 21702 USA
[2] Tel Aviv Univ, Dept Human Mol Genet & Biochem, Sackler Sch Med, IL-69978 Tel Aviv, Israel
基金
美国国家卫生研究院;
关键词
HIGH-AFFINITY INTERACTION; ALLOSTERIC ACTIVATION; HYPERVARIABLE REGION; TISSUE-SPECIFICITY; PI3K ACTIVATION; K-RAS; CALMODULIN; KINASES; CANCER; KSR;
D O I
10.1016/j.sbi.2020.01.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here, we review mechanisms of Ras spatiotemporal clustering with PI3K alpha and Raf at the membrane. The large RTK-Ras-PI3K alpha lipid kinase assembly is at the membrane to generate signaling lipid PIP3. Raf, but not PI3K alpha, has long linker extending from the membrane to the kinase domain. This disordered linker stretches into the cytoplasm where Raf's kinase domain side-to-side dimerization and activation is allosterically-driven by MEK under KSR dimers control. The cytoplasm, but not the crowded membrane surface, can accommodate the large Raf's activation and MAPK signaling assemblies, and Raf's disordered linker brings them there. Further, Raf's activation, but not PI3K alpha's, requires kinase domain dimerization; Ras nanoclusters accomplishing this necessitate Raf's long linkers. Thus, biophysical and functional constraints shape Ras spatiotemporal assemblies.
引用
收藏
页码:140 / 148
页数:9
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