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通过冷冻电镜鉴定真核生物核糖体上的多功能支架蛋白RACK1。

Identification of the versatile scaffold protein RACK1 on the eukaryotic ribosome by cryo-EM.

作者信息

Sengupta Jayati, Nilsson Jakob, Gursky Richard, Spahn Christian M T, Nissen Poul, Frank Joachim

机构信息

Health Research, Inc., Wadsworth Center, New York State Department of Health, Empire State Plaza, Albany, New York 12201-0509, USA.

出版信息

Nat Struct Mol Biol. 2004 Oct;11(10):957-62. doi: 10.1038/nsmb822. Epub 2004 Aug 29.

Abstract

RACK1 serves as a scaffold protein for a wide range of kinases and membrane-bound receptors. It is a WD-repeat family protein and is predicted to have a beta-propeller architecture with seven blades like a Gbeta protein. Mass spectrometry studies have identified its association with the small subunit of eukaryotic ribosomes and, most recently, it has been shown to regulate initiation by recruiting protein kinase C to the 40S subunit. Here we present the results of a cryo-EM study of the 80S ribosome that positively locate RACK1 on the head region of the 40S subunit, in the immediate vicinity of the mRNA exit channel. One face of RACK1 exposes the WD-repeats as a platform for interactions with kinases and receptors. Using this platform, RACK1 can recruit other proteins to the ribosome.

摘要

RACK1作为多种激酶和膜结合受体的支架蛋白。它是一种WD重复家族蛋白,预计具有类似Gβ蛋白的七叶β-螺旋桨结构。质谱研究已确定它与真核核糖体的小亚基有关联,最近还表明它通过将蛋白激酶C招募到40S亚基来调节起始过程。在此,我们展示了一项关于80S核糖体的冷冻电镜研究结果,该研究明确将RACK1定位在40S亚基的头部区域,紧邻mRNA出口通道。RACK1的一个面暴露WD重复序列,作为与激酶和受体相互作用的平台。利用这个平台,RACK1可以将其他蛋白质招募到核糖体上。

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