Literature DB >> 10388753

Conformational changes of the in situ nuclear pore complex.

H Wang1, D E Clapham.   

Abstract

By bridging the double membrane separating the cell nucleus and cytoplasm, nuclear pore complexes (NPCs) are crucial pathways for the exchange of ions, proteins, and RNA between these two cellular compartments. A structure in the central lumen of the NPC, called the nuclear transport protein, central granule, or nuclear plug, appeared to gate diffusion of intermediate-sized molecules (10-40 kDa) across the nuclear membranes. Visualization of the NPC required drying and fixation of the specimen for electron and atomic force microscopy (AFM), a requirement that has raised doubts about the physiological relevance of the observation. Here we present AFM images of the outer nuclear membranes and NPCs of Xenopus laevis oocytes under more physiological conditions. Measured under a variety of Ca2+ depletion conditions, the central granule appeared to occupy and occlude the lumen of the pore in >80% of NPCs compared to <10% in controls. In a few instances images were obtained of the same NPCs as the solution was changed from control saline to store depletion conditions, and finally to store repletion conditions. We conclude that the central lumen of the nuclear pore complex undergoes a conformational change in response to depletion of nuclear cisternal Ca2+ levels.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10388753      PMCID: PMC1300325          DOI: 10.1016/S0006-3495(99)76885-2

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  29 in total

Review 1.  Nucleocytoplasmic transport: the soluble phase.

Authors:  I W Mattaj; L Englmeier
Journal:  Annu Rev Biochem       Date:  1998       Impact factor: 23.643

2.  Conformational states of the nuclear pore complex induced by depletion of nuclear Ca2+ stores.

Authors:  C Perez-Terzic; J Pyle; M Jaconi; L Stehno-Bittel; D E Clapham
Journal:  Science       Date:  1996-09-27       Impact factor: 47.728

Review 3.  Three-dimensional surface structure analysis of the nucleus.

Authors:  T D Allen; S A Rutherford; G R Bennion; C Wiese; S Riepert; E Kiseleva; M W Goldberg
Journal:  Methods Cell Biol       Date:  1998       Impact factor: 1.441

4.  ATP-Induced shape change of nuclear pores visualized with the atomic force microscope.

Authors:  A Rakowska; T Danker; S W Schneider; H Oberleithner
Journal:  J Membr Biol       Date:  1998-05-15       Impact factor: 1.843

Review 5.  Nuclear calcium and the regulation of the nuclear pore complex.

Authors:  C Perez-Terzic; M Jaconi; D E Clapham
Journal:  Bioessays       Date:  1997-09       Impact factor: 4.345

Review 6.  Functional organization of the nuclear envelope.

Authors:  L Gerace; B Burke
Journal:  Annu Rev Cell Biol       Date:  1988

7.  A major glycoprotein of the nuclear pore complex is a membrane-spanning polypeptide with a large lumenal domain and a small cytoplasmic tail.

Authors:  U F Greber; A Senior; L Gerace
Journal:  EMBO J       Date:  1990-05       Impact factor: 11.598

8.  The permeability of the nuclear envelope in dividing and nondividing cell cultures.

Authors:  C M Feldherr; D Akin
Journal:  J Cell Biol       Date:  1990-07       Impact factor: 10.539

9.  Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape.

Authors:  L W Jiang; M Schindler
Journal:  J Cell Biol       Date:  1988-01       Impact factor: 10.539

10.  Active nuclear import and export is independent of lumenal Ca2+ stores in intact mammalian cells.

Authors:  C Strübing; D E Clapham
Journal:  J Gen Physiol       Date:  1999-02       Impact factor: 4.086

View more
  26 in total

1.  Distinct ion channel classes are expressed on the outer nuclear envelope of T- and B-lymphocyte cell lines.

Authors:  A Franco-Obregón; H W Wang; D E Clapham
Journal:  Biophys J       Date:  2000-07       Impact factor: 4.033

2.  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

3.  Modulation of nuclear pore topology by transport modifiers.

Authors:  Rainer D Jäggi; Alfredo Franco-Obregón; Petra Mühlhäusser; Franziska Thomas; Ulrike Kutay; Klaus Ensslin
Journal:  Biophys J       Date:  2003-01       Impact factor: 4.033

4.  Real-time imaging of nuclear permeation by EGFP in single intact cells.

Authors:  Xunbin Wei; Vanessa G Henke; Carsten Strübing; Edward B Brown; David E Clapham
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

5.  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

6.  From the trap to the basket: getting to the bottom of the nuclear pore complex.

Authors:  Roderick Y H Lim; Ueli Aebi; Daniel Stoffler
Journal:  Chromosoma       Date:  2006-01-10       Impact factor: 4.316

Review 7.  Route of glucocorticoid-induced macromolecules across the nuclear envelope as viewed by atomic force microscopy.

Authors:  Victor Shahin
Journal:  Pflugers Arch       Date:  2006-05-31       Impact factor: 3.657

8.  An historical perspective on cell mechanics.

Authors:  Andrew E Pelling; Michael A Horton
Journal:  Pflugers Arch       Date:  2007-12-07       Impact factor: 3.657

9.  Apoptosis leads to a degradation of vital components of active nuclear transport and a dissociation of the nuclear lamina.

Authors:  A Kramer; I Liashkovich; H Oberleithner; S Ludwig; I Mazur; V Shahin
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-04       Impact factor: 11.205

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.