The Mgr2 subunit of the TIM23 complex regulates membrane insertion of marginal stop-transfer signals in the mitochondrial inner membrane

被引:13
|
作者
Lee, Seoeun [1 ]
Lee, Hunsang [1 ,2 ]
Yoo, Suji [1 ]
Leva, Raffaele [3 ]
van der Laan, Martin [4 ]
von Heijne, Gunnar [5 ]
Kim, Hyun [1 ]
机构
[1] Seoul Natl Univ, Sch Biol Sci, Bldg 504-421, Seoul 08826, South Korea
[2] Donnelly Ctr, Toronto, ON, Canada
[3] Univ Toulouse, Ctr Biol Integrat, Lab Microbiol & Genet Mol, CNRS,UPS, Toulouse, France
[4] Saarland Univ, Ctr Mol Signaling, PZMS, Med Biochem & Mol Biol, Homburg, Germany
[5] Stockholm Univ, Dept Biochem & Biophys, Stockholm, Sweden
基金
新加坡国家研究基金会;
关键词
hydrophobicity; import; Mgm1; TIM23; yeast; PRESEQUENCE TRANSLOCASE; INTERMEMBRANE SPACE; RECOGNITION; IMPORT; CYTOCHROME-B2; MORPHOLOGY; PROTEINS; HELICES; MGM1;
D O I
10.1002/1873-3468.13692
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
The TIM23 complex mediates membrane insertion of presequence-containing mitochondrial proteins via a stop-transfer mechanism. Stop-transfer signals consist of hydrophobic transmembrane segments and flanking charges. Mgr2 functions as a lateral gatekeeper of the TIM23 complex. However, it remains elusive which features of stop-transfer signals are discriminated by Mgr2. To determine the effects of Mgr2 on the TIM23-mediated stop-transfer pathway, we measured membrane insertion of model transmembrane segments of varied hydrophobicity and flanking charges in Mgr2-deletion or -overexpression yeast strains. We found that upon deletion of Mgr2, the threshold hydrophobicity for membrane insertion, as well as the requirement for matrix-facing positive charges, is reduced. These results imply that the Mgr2-mediated gatekeeper function is important for controlling membrane sorting of marginal stop-transfer signals.
引用
收藏
页码:1081 / 1087
页数:7
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