Halic Mario, Gartmann Marco, Schlenker Oliver, Mielke Thorsten, Pool Martin R, Sinning Irmgard, Beckmann Roland
Institute of Biochemistry, Charité, University Medical School Berlin, Monbijoustrasse 2, 10117 Berlin, Germany.
Science. 2006 May 5;312(5774):745-7. doi: 10.1126/science.1124864.
Signal sequences of secretory and membrane proteins are recognized by the signal recognition particle (SRP) as they emerge from the ribosome. This results in their targeting to the membrane by docking with the SRP receptor, which facilitates transfer of the ribosome to the translocon. Here, we present the 8 angstrom cryo-electron microscopy structure of a "docking complex" consisting of a SRP-bound 80S ribosome and the SRP receptor. Interaction of the SRP receptor with both SRP and the ribosome rearranged the S domain of SRP such that a ribosomal binding site for the translocon, the L23e/L35 site, became exposed, whereas Alu domain-mediated elongation arrest persisted.
分泌蛋白和膜蛋白的信号序列在从核糖体出现时被信号识别颗粒(SRP)识别。这导致它们通过与SRP受体对接而靶向膜,SRP受体促进核糖体转移到易位子。在此,我们展示了由结合SRP的80S核糖体和SRP受体组成的“对接复合物”的8埃冷冻电子显微镜结构。SRP受体与SRP和核糖体的相互作用重新排列了SRP的S结构域,使得易位子的核糖体结合位点,即L23e/L35位点暴露,而Alu结构域介导的延伸停滞持续存在。