Literature DB >> 17164246

Passive and facilitated transport in nuclear pore complexes is largely uncoupled.

Bracha Naim1, Vlad Brumfeld, Ruti Kapon, Vladimir Kiss, Reinat Nevo, Ziv Reich.   

Abstract

Nuclear pore complexes provide the sole gateway for the exchange of material between nucleus and cytoplasm of interphase eukaryotic cells. They support two modes of transport: passive diffusion of ions, metabolites, and intermediate-sized macromolecules and facilitated, receptor-mediated translocation of proteins, RNA, and ribonucleoprotein complexes. It is generally assumed that both modes of transport occur through a single diffusion channel located within the central pore of the nuclear pore complex. To test this hypothesis, we studied the mutual effects between transporting molecules utilizing either the same or different modes of translocation. We find that the two modes of transport do not interfere with each other, but molecules utilizing a particular mode of transport do hinder motion of others utilizing the same pathway. We therefore conclude that the two modes of transport are largely segregated.

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Year:  2006        PMID: 17164246     DOI: 10.1074/jbc.M608329200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  43 in total

1.  Fluorescent recovery after photobleaching (FRAP) analysis of nuclear export rates identifies intrinsic features of nucleocytoplasmic transport.

Authors:  Francesco Cardarelli; Luca Tosti; Michela Serresi; Fabio Beltram; Ranieri Bizzarri
Journal:  J Biol Chem       Date:  2011-12-21       Impact factor: 5.157

2.  Self-regulated viscous channel in the nuclear pore complex.

Authors:  Jiong Ma; Alexander Goryaynov; Ashapurna Sarma; Weidong Yang
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-23       Impact factor: 11.205

3.  Facilitated transport and diffusion take distinct spatial routes through the nuclear pore complex.

Authors:  Jindriska Fiserova; Shane A Richards; Susan R Wente; Martin W Goldberg
Journal:  J Cell Sci       Date:  2010-07-20       Impact factor: 5.285

4.  Atomic force microscopy visualises a hydrophobic meshwork in the central channel of the nuclear pore.

Authors:  Armin Kramer; Ivan Liashkovich; Yvonne Ludwig; Victor Shahin
Journal:  Pflugers Arch       Date:  2007-12-04       Impact factor: 3.657

Review 5.  Biology and biophysics of the nuclear pore complex and its components.

Authors:  Roderick Y H Lim; Katharine S Ullman; Birthe Fahrenkrog
Journal:  Int Rev Cell Mol Biol       Date:  2008       Impact factor: 6.813

6.  Cargo surface hydrophobicity is sufficient to overcome the nuclear pore complex selectivity barrier.

Authors:  Bracha Naim; David Zbaida; Shlomi Dagan; Ruti Kapon; Ziv Reich
Journal:  EMBO J       Date:  2009-08-13       Impact factor: 11.598

7.  Nanoscale mechanism of molecular transport through the nuclear pore complex as studied by scanning electrochemical microscopy.

Authors:  Jiyeon Kim; Anahita Izadyar; Nikoloz Nioradze; Shigeru Amemiya
Journal:  J Am Chem Soc       Date:  2013-01-30       Impact factor: 15.419

8.  A cell-penetrating peptide suppresses the hypoxia inducible factor-1 function by binding to the helix-loop-helix domain of the aryl hydrocarbon receptor nuclear translocator.

Authors:  Yu Wang; John D Thompson; William K Chan
Journal:  Chem Biol Interact       Date:  2013-02-27       Impact factor: 5.192

9.  The mechanistic role of alpha-synuclein in the nucleus: impaired nuclear function caused by familial Parkinson's disease SNCA mutations.

Authors:  Vivian Chen; Malik Moncalvo; Dominic Tringali; Lidia Tagliafierro; Ahila Shriskanda; Ekaterina Ilich; Wendy Dong; Boris Kantor; Ornit Chiba-Falek
Journal:  Hum Mol Genet       Date:  2020-11-04       Impact factor: 6.150

10.  Autonomy and robustness of translocation through the nuclear pore complex: a single-molecule study.

Authors:  Thomas Dange; David Grünwald; Antje Grünwald; Reiner Peters; Ulrich Kubitscheck
Journal:  J Cell Biol       Date:  2008-09-29       Impact factor: 10.539

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