Scaffold Proteins: Hubs for Controlling the Flow of Cellular Information

被引:727
作者
Good, Matthew C. [1 ]
Zalatan, Jesse G. [1 ]
Lim, Wendell A. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Ctr Syst & Synthet Biol, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94158 USA
关键词
FUS3 MAP KINASE; SIGNALING SPECIFICITY; BINDING DOMAIN; STE5; COMPLEX; ACTIVATION; SUBSTRATE; RECEPTOR; MECHANISM; PATHWAYS;
D O I
10.1126/science.1198701
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The spatial and temporal organization of molecules within a cell is critical for coordinating the many distinct activities carried out by the cell. In an increasing number of biological signaling processes, scaffold proteins have been found to play a central role in physically assembling the relevant molecular components. Although most scaffolds use a simple tethering mechanism to increase the efficiency of interaction between individual partner molecules, these proteins can also exert complex allosteric control over their partners and are themselves the target of regulation. Scaffold proteins offer a simple, flexible strategy for regulating selectivity in pathways, shaping output behaviors, and achieving new responses from preexisting signaling components. As a result, scaffold proteins have been exploited by evolution, pathogens, and cellular engineers to reshape cellular behavior.
引用
收藏
页码:680 / 686
页数:7
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