Characterisation of the passive permeability barrier of nuclear pore complexes

被引:277
作者
Mohr, Dagmar [2 ]
Frey, Steffen
Fischer, Torsten [2 ]
Guettler, Thomas
Goerlich, Dirk [1 ,2 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Cellular Logist, D-37077 Gottingen, Germany
[2] Heidelberg Univ, ZMBH, D-6900 Heidelberg, Germany
关键词
hydrogel; importin; nuclear pore; selective phase model; wheat germ agglutinin; WHEAT-GERM-AGGLUTININ; IMPORTIN-BETA; PROTEIN IMPORT; TRANSPORT; BINDING; ARCHITECTURE; IDENTIFICATION; NUCLEOPORINS; INHIBITION; RANGTP;
D O I
10.1038/emboj.2009.200
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
Nuclear pore complexes (NPCs) restrict uncontrolled nucleocytoplasmic fluxes of inert macromolecules but permit facilitated translocation of nuclear transport receptors and their cargo complexes. We probed the passive barrier of NPCs and observed sieve-like properties with a dominating mesh or channel radius of 2.6 nm, which is narrower than proposed earlier. A small fraction of diffusion channels has a wider opening, explaining the very slow passage of larger molecules. The observed dominant passive diameter approximates the distance of adjacent hydrophobic clusters of FG repeats, supporting the model that the barrier is made of FG repeat domains cross-linked with a spacing of an FG repeat unit length. Wheat germ agglutinin and the dominant-negative importin beta(45-462) fragment were previously regarded as selective inhibitors of facilitated NPC passage. We now observed that they do not distinguish between the passive and the facilitated mode. Instead, their inhibitory effect correlates with the size of the NPC-passing molecule. They have little effect on small species, inhibit the passage of green fluorescent protein-sized objects >10-fold and virtually block the translocation of larger ones. This suggests that passive and facilitated NPC passage proceed through one and the same permeability barrier. The EMBO Journal (2009) 28, 2541-2553. doi: 10.1038/emboj.2009.200; Published online 13 August 2009 Subject Categories: membranes & transport
引用
收藏
页码:2541 / 2553
页数:13
相关论文
共 42 条
  • [31] The permeability barrier of nuclear pore complexes appears to operate via hydrophobic exclusion
    Ribbeck, K
    Görlich, D
    [J]. EMBO JOURNAL, 2002, 21 (11) : 2664 - 2671
  • [32] NTF2 mediates nuclear import of Ran
    Ribbeck, K
    Lipowsky, G
    Kent, HM
    Stewart, M
    Görlich, D
    [J]. EMBO JOURNAL, 1998, 17 (22) : 6587 - 6598
  • [33] Kinetic analysis of translocation through nuclear pore complexes
    Ribbeck, K
    Görlich, D
    [J]. EMBO JOURNAL, 2001, 20 (06) : 1320 - 1330
  • [34] The nuclear pore complex as a transport machine
    Rout, MP
    Aitchison, JD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) : 16593 - 16596
  • [35] Major binding sites for the nuclear import receptor are the internal nucleoporin Nup153 and the adjacent nuclear filament protein Tpr
    Shah, S
    Tugendreich, S
    Forbes, D
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (01) : 31 - 49
  • [36] Nuclear import of Ran is mediated by the transport factor NTF2
    Smith, A
    Brownawell, A
    Macara, IG
    [J]. CURRENT BIOLOGY, 1998, 8 (25) : 1403 - 1406
  • [37] Cryo-electron tomography provides novel insights into nuclear pore architecture: Implications for nucleocytoplasmic transport
    Stoffler, D
    Feja, B
    Fahrenkrog, B
    Walz, J
    Typke, D
    Aebi, U
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2003, 328 (01) : 119 - 130
  • [38] Dynamic nuclear pore complexes: Life on the edge
    Tran, Elizabeth J.
    Wente, Susan R.
    [J]. CELL, 2006, 125 (06) : 1041 - 1053
  • [39] Structural view of the Ran-importin β interaction at 2.3 Å resolution
    Vetter, IR
    Arndt, A
    Kutay, U
    Görlich, D
    Wittinghofer, A
    [J]. CELL, 1999, 97 (05) : 635 - 646
  • [40] RanGTP mediates nuclear pore complex assembly
    Walther, TC
    Askjaer, P
    Gentzel, M
    Habermann, A
    Griffiths, G
    Wilm, M
    Mattaj, IW
    Hetzer, M
    [J]. NATURE, 2003, 424 (6949) : 689 - 694