Literature DB >> 7739040

Structural plasticity of the nuclear pore complex.

C W Akey1.   

Abstract

The nuclear pore complex (NPC) is strategically located at continuous junctions of the inner and outer nuclear membranes to catalyze macromolecular transport, without impending the diffusion of small molecules. In this paper, the structural plasticity of 4412 NPCs in isolated nuclear envelopes has been evaluated, utilizing correspondence analysis, classification and difference mapping. The data are grouped into seven clusters comprising two major groups, based on the degree of radial compaction within spokes and the symmetry of the inner spoke ring. The results have been correlated with differences in spoke domain packing observed in two published three-dimensional maps suggesting that symmetrical detergent-extracted NPCs are similar, but not identical to the most probable in vivo structure. A model is proposed in which spoke architecture is responsive to changes in the turgor pressure of the nuclear envelope. For example, detergent extraction may allow the outward facing domains of each spoke to adopt a radially-extended configuration while osmotic swelling may induce an inwards displacement, resulting in a radially compact spoke. Difference maps between approximately 822 symmetric projections of NPCs in membranes and after detergent-extraction have localized the nuclear envelope border. The data place limits on the radial and circumferential dimensions of diffusion channels (approximately 0 to 20 A x 190 A), proposed to reside at the pore periphery. The results confirm the observation that each spoke penetrates the nuclear envelope, linking up with the radial arms to form a "lumenal ring". Finally, putative closed, open and in-transit forms of the transporter are found with the same relative frequency in membrane-associated NPCs with radially compact or extended spokes; hence spoke deformations in isolated envelopes may be induced by experimental factors. However, concerted movements of the spoke domains (if reversible) may be utilized in the biological function of the NPC and some examples are given.

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Year:  1995        PMID: 7739040     DOI: 10.1016/s0022-2836(95)80050-6

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  36 in total

1.  Quantitative topographical analysis of nuclear pore complex function using scanning force microscopy.

Authors:  Rainer D Jäggi; Alfredo Franco-Obregón; Klaus Ensslin
Journal:  Biophys J       Date:  2003-12       Impact factor: 4.033

2.  Binding dynamics of structural nucleoporins govern nuclear pore complex permeability and may mediate channel gating.

Authors:  Nataliya Shulga; David S Goldfarb
Journal:  Mol Cell Biol       Date:  2003-01       Impact factor: 4.272

3.  Regulation of nuclear pore complex conformation by IP(3) receptor activation.

Authors:  David Moore-Nichols; Anne Arnott; Robert C Dunn
Journal:  Biophys J       Date:  2002-09       Impact factor: 4.033

4.  A bimodal distribution of two distinct categories of intrinsically disordered structures with separate functions in FG nucleoporins.

Authors:  Justin Yamada; Joshua L Phillips; Samir Patel; Gabriel Goldfien; Alison Calestagne-Morelli; Hans Huang; Ryan Reza; Justin Acheson; Viswanathan V Krishnan; Shawn Newsam; Ajay Gopinathan; Edmond Y Lau; Michael E Colvin; Vladimir N Uversky; Michael F Rexach
Journal:  Mol Cell Proteomics       Date:  2010-04-05       Impact factor: 5.911

5.  Structural and functional analysis of Nup120 suggests ring formation of the Nup84 complex.

Authors:  Hyuk-Soo Seo; Yingli Ma; Erik W Debler; Daniel Wacker; Stephan Kutik; Günter Blobel; André Hoelz
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-11       Impact factor: 11.205

6.  Structure of a trimeric nucleoporin complex reveals alternate oligomerization states.

Authors:  Vivien Nagy; Kuo-Chiang Hsia; Erik W Debler; Martin Kampmann; Andrew M Davenport; Günter Blobel; André Hoelz
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-01       Impact factor: 11.205

Review 7.  Toward the atomic structure of the nuclear pore complex: when top down meets bottom up.

Authors:  André Hoelz; Joseph S Glavy; Martin Beck
Journal:  Nat Struct Mol Biol       Date:  2016-06-06       Impact factor: 15.369

Review 8.  The nuclear pore complex.

Authors:  A Heese-Peck; N V Raikhel
Journal:  Plant Mol Biol       Date:  1998-09       Impact factor: 4.076

9.  A novel fluorescence-based genetic strategy identifies mutants of Saccharomyces cerevisiae defective for nuclear pore complex assembly.

Authors:  M Bucci; S R Wente
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

10.  Structure, dynamics, evolution, and function of a major scaffold component in the nuclear pore complex.

Authors:  Parthasarathy Sampathkumar; Seung Joong Kim; Paula Upla; William J Rice; Jeremy Phillips; Benjamin L Timney; Ursula Pieper; Jeffrey B Bonanno; Javier Fernandez-Martinez; Zhanna Hakhverdyan; Natalia E Ketaren; Tsutomu Matsui; Thomas M Weiss; David L Stokes; J Michael Sauder; Stephen K Burley; Andrej Sali; Michael P Rout; Steven C Almo
Journal:  Structure       Date:  2013-03-14       Impact factor: 5.006

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