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Identification of the versatile scaffold protein RACK1 on the eukaryotic ribosome by cryo-EM
被引:0
|作者:
Jayati Sengupta
Jakob Nilsson
Richard Gursky
Christian M T Spahn
Poul Nissen
Joachim Frank
机构:
[1] Health Research,New York State Department of Health
[2] Inc.,New York State Department of Health
[3] Wadsworth Center,Department of Biomedical Sciences
[4] Empire State Plaza,Department of Molecular Biology
[5] Howard Hughes Medical Institute,undefined
[6] Wadsworth Center,undefined
[7] Empire State Plaza,undefined
[8] State University of New York at Albany,undefined
[9] Empire State Plaza,undefined
[10] University of Aarhus,undefined
[11] Gustav Wieds vej 10C,undefined
[12] Institut für Medizinische Physik und Biophysik der Charité,undefined
[13] Humboldt Universität zu Berlin,undefined
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摘要:
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 β-propeller architecture with seven blades like a Gβ 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.
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页码:957 / 962
页数:5
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