Literature DB >> 11719846

Electrophoretic plugging of nuclear pores by using the nuclear hourglass technique.

T Danker1, V Shahin, A Schlune, C Schäfer, H Oberleithner.   

Abstract

The nuclear hourglass technique (NHT) was recently introduced as a novel technique that measures the electrical nuclear envelope (NE) conductance of isolated Xenopus laevis oocyte nuclei. The main conclusion drawn from NHT work so far is that nuclear pore complexes (NPCs) of oocytes are in an electrically open state under physiological conditions, with a mean conductance of 1.7 nS per NPC. Since nuclear patch-clamp data indicate that usually NPCs are electrically closed, our work has been challenged by the notion that NHT cannot assure a high resistance seal ("gigaseal") between glass wall and NE like that required for patch-clamp experiments. Thus, NHT could have dramatically underestimated NE electrical resistance. Here we demonstrate that NHT does not require a gigaseal for accurate NE conductance measurements. In addition, we present experimental conditions where mean single NPC electrical conductance is reduced 26-fold due to electrophoretic plugging by negatively charged nucleoplasmic macromolecules. In addition, data indicate that under physiological conditions (i.e., when macromolecules are offered in the cytosolic solution) the nuclear surface is heavily folded, underestimating "true" NE surface by a factor of 2.6. When "true" NE surface area is taken into consideration, modified values of mean single NPC conductances of 654 pS for electrically open conditions and 25 pS for electrically plugged conditions can be calculated. We conclude that the large overall NE conductance detected with the nuclear hourglass technique in intact Xenopus laevis oocyte nuclei can be explained by the sum of single NPC conductances in the pS range, as long as open probability is high. This confirms previous patch-clamp work concerning single NPC conductance, but disagrees with the view that mean open probability of NPC channels is usually low.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11719846     DOI: 10.1007/s00232-001-0078-1

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  8 in total

1.  Passive transport of macromolecules through Xenopus laevis nuclear envelope.

Authors:  K Enss; T Danker; A Schlune; I Buchholz; H Oberleithner
Journal:  J Membr Biol       Date:  2003-12-01       Impact factor: 1.843

2.  Intracellular calcium: a prerequisite for aldosterone action.

Authors:  C Schäfer; V Shahin; L Albermann; H Schillers; M J Hug; H Oberleithner
Journal:  J Membr Biol       Date:  2003-12-01       Impact factor: 1.843

3.  Ethanol alters access to the cell nucleus.

Authors:  Claudia Schäfer; Yvonne Ludwig; Victor Shahin; Armin Kramer; Philippe Carl; Hermann Schillers; Hans Oberleithner
Journal:  Pflugers Arch       Date:  2006-10-17       Impact factor: 3.657

4.  Aldosterone signaling pathway across the nuclear envelope.

Authors:  C Schäfer; V Shahin; L Albermann; M J Hug; J Reinhardt; H Schillers; S W Schneider; H Oberleithner
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-30       Impact factor: 11.205

Review 5.  Calcium signaling in synapse-to-nucleus communication.

Authors:  Anna M Hagenston; Hilmar Bading
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-11-01       Impact factor: 10.005

6.  Gating transitions in bacterial ion channels measured at 3 microns resolution.

Authors:  George Shapovalov; Henry A Lester
Journal:  J Gen Physiol       Date:  2004-08       Impact factor: 4.086

7.  Transient permeability leak of nuclear envelope induced by aldosterone.

Authors:  I Buchholz; K Enss; C Schafer; A Schlune; V Shahin; H Oberleithner
Journal:  J Membr Biol       Date:  2004-06-01       Impact factor: 1.843

8.  Characterization of Single-Nucleus Electrical Properties by Microfluidic Constriction Channel.

Authors:  Hongyan Liang; Yi Zhang; Deyong Chen; Huiwen Tan; Yu Zheng; Junbo Wang; Jian Chen
Journal:  Micromachines (Basel)       Date:  2019-10-31       Impact factor: 2.891

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.