Architecture of the protein-conducting channel associated with the translating 80S ribosome

被引:310
作者
Beckmann, R
Spahn, CMT
Eswar, N
Helmers, J
Penczek, PA
Sali, A
Frank, J
Blobel, G
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Cell Biol Lab, New York, NY 10021 USA
[2] Hlth Res Inc, Howard Hughes Med Inst, Albany, NY 12201 USA
[3] New York State Dept Hlth, Wadsworth Ctr Labs & Res, Albany, NY 12201 USA
[4] Rockefeller Univ, Pels Family Ctr Biochem & Struct Biol, Lab Mol Biophys, New York, NY 10021 USA
[5] Univ Texas, Sch Med, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[6] SUNY Albany, Dept Biomed Sci, Albany, NY 12222 USA
[7] Humboldt Univ, Charite, Inst Biochem, D-10117 Berlin, Germany
关键词
D O I
10.1016/S0092-8674(01)00541-4
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
In vitro assembled yeast ribosome-nascent chain complexes (RNCs) containing a signal sequence in the nascent chain were immunopurified and reconstituted with the purified protein-conducting channel (PCC) of yeast endoplasmic reticulum, the Sec61 complex. A cryo-EM reconstruction of the RNC-Sec61 complex at 15.4 Angstrom resolution shows a tRNA in the P site. Distinct rRNA elements and proteins of the large ribosomal subunit form four connections with the PCC across a gap of about 10-20 Angstrom. Binding of the PCC influences the position of the highly dynamic rRNA expansion segment 27. The RNC-bound Sec61 complex has a compact appearance and was estimated to be a trimer. We propose a binary model of cotranslational translocation entailing only two basic functional states of the translating ribosome-channel complex.
引用
收藏
页码:361 / 372
页数:12
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