The TIM23 mitochondrial protein import complex: function and dysfunction

被引:0
|
作者
Keren Demishtein-Zohary
Abdussalam Azem
机构
[1] Tel Aviv University,Department of Biochemistry and Molecular Biology, The George S. Wise Faculty of Life Sciences
来源
Cell and Tissue Research | 2017年 / 367卷
关键词
Mitochondrial protein import; TOM complex; TIM23 complex; Import motor; Pam complex;
D O I
暂无
中图分类号
学科分类号
摘要
Mitochondria acquire the majority of their proteins from the cytosol in a process that is mediated by intricate multimeric machineries designed to allow proteins to cross and/or to insert themselves into the two mitochondrial membranes. Ongoing studies carried out in yeast over the past few decades have led to the discovery of numerous protein components that constitute several mitochondrial translocases. One of these complexes, the mitochondrial TIM23, is the major translocase for matrix proteins and is the focus of this review. The components of the TIM23 complex are categorized into four functional types. The first type plays the role of receptor for preproteins in the intermembrane space. The second type forms the actual channel that allows proteins to cross the inner mitochondrial membrane. The third species functions as part of the motor that mediates the final steps of import across the inner membrane. Additional components play regulatory roles orchestrating the action of this myriad of subunits. Recent studies provide new insights into the function of the mammalian TIM23 complex and the role that it plays under pathological conditions.
引用
收藏
页码:33 / 41
页数:8
相关论文
共 50 条
  • [1] The TIM23 mitochondrial protein import complex: function and dysfunction
    Demishtein-Zohary, Keren
    Azem, Abdussalam
    CELL AND TISSUE RESEARCH, 2017, 367 (01) : 33 - 41
  • [2] Structural basis of mitochondrial protein import by the TIM23 complex
    Sim, Sue Im
    Chen, Yuanyuan
    Lynch, Diane L.
    Gumbart, James C.
    Park, Eunyong
    NATURE, 2023, 621 (7979) : 620 - +
  • [3] Structural basis of mitochondrial protein import by the TIM23 complex
    Sue Im Sim
    Yuanyuan Chen
    Diane L. Lynch
    James C. Gumbart
    Eunyong Park
    Nature, 2023, 621 : 620 - 626
  • [4] Interaction of Tim23 with Tim50 Is Essential for Protein Translocation by the Mitochondrial TIM23 Complex
    Gevorkyan-Airapetov, Lada
    Zohary, Keren
    Popov-Celeketic, Dusan
    Mapa, Koyeli
    Hell, Kai
    Neupert, Walter
    Azem, Abdussalam
    Mokranjac, Dejana
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (08) : 4865 - 4872
  • [5] Role of the import motor in insertion of transmembrane segments by the mitochondrial TIM23 complex
    Popov-Celeketic, Dusan
    Waegemann, Karin
    Mapa, Koyeli
    Neupert, Walter
    Mokranjac, Dejana
    EMBO REPORTS, 2011, 12 (06) : 542 - 548
  • [6] Cardiolipin mediates membrane and channel interactions of the mitochondrial TIM23 protein import complex receptor Tim50
    Malhotra, Ketan
    Modak, Arnab
    Nangia, Shivangi
    Daman, Tyler H.
    Gunsel, Umut
    Robinson, Victoria L.
    Mokranjac, Dejana
    May, Eric R.
    Alder, Nathan N.
    SCIENCE ADVANCES, 2017, 3 (09):
  • [7] The many faces of the mitochondrial TIM23 complex
    Mokranjac, Dejana
    Neupert, Walter
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2010, 1797 (6-7): : 1045 - 1054
  • [8] Association of the Tim14•Tim16 subcomplex with the TIM23 translocase is crucial for function of the mitochondrial protein import motor
    Mokranjac, Dejana
    Berg, Annette
    Adam, Alexander
    Neupert, Walter
    Hell, Kai
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (25) : 18037 - 18045
  • [9] Protein import into and across the mitochondrial inner membrane: role of the TIM23 and TIM22 translocons
    Jensen, RE
    Dunn, CD
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2002, 1592 (01): : 25 - 34
  • [10] Tim17p regulates the twin pore structure and voltage gating of the mitochondrial protein import complex TIM23
    Martinez-Caballero, Sonia
    Grigoriev, Sell M.
    Herrmann, Johannes M.
    Campo, Maria Luisa
    Kinnally, Kathleen W.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (06) : 3584 - 3593