Direct interaction of YidC with the Sec-independent Pf3 coat protein during its membrane protein insertion

被引:115
作者
Chen, MY
Samuelson, JC
Jiang, FL
Muller, M
Kuhn, A
Dalbey, RE
机构
[1] Ohio State Univ, Dept Chem, Ohio State Biochem Program, Columbus, OH 43210 USA
[2] Ohio State Univ, Prot Res Grp, Columbus, OH 43210 USA
[3] Univ Hohenheim, Inst Microbiol & Mol Biol, D-70593 Stuttgart, Germany
[4] Univ Freiburg, Inst Biochem & Mol Biol, D-79104 Freiburg, Germany
关键词
D O I
10.1074/jbc.M110644200
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
YidC is a newly defined translocase component that mediates the insertion of proteins into the membrane bilayer. How YidC functions in the insertion process is not known. In this study, we report that the Sec-independent Pf3 coat protein requires the YidC protein specifically for the membrane translocation step. Using photocrosslinking techniques and ribosome-bound Pf3 coat derivatives with an extended carboxyl-terminal region, we found that the transmembrane region of the Pf3 coat protein physically interacts with YidC and the bacterial signal recognition particle Ffh component. We also find that in the insertion pathway, Pf3 coat interacts strongly with YidC only after its transmembrane segment is fully exposed outside the ribosome tunnel. Interaction between Pf3 coat and YidC occurs even in the absence of the proton motive force and with a Pf3 coat mutant that is defective in transmembrane insertion. Our study demonstrates that YidC can directly interact with a Sec-independent membrane protein, and the role of YidC is at the stage of folding the Pf3 protein into a transmembrane configuration.
引用
收藏
页码:7670 / 7675
页数:6
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