Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-26T05:35:29.988Z Has data issue: false hasContentIssue false
  • English
  • Français

Nuclear Pore Transport: Insight in Situ

Published online by Cambridge University Press:  02 July 2020

U. Aebi ,
D. Stoffler ,
B. Feja  and
K. Goldie
U. Aebi
Affiliation:
Biozentrum, M.E. Miiller Institute, University of Basel, CH-4056Basel, Switzerland
D. Stoffler
Affiliation:
Biozentrum, M.E. Miiller Institute, University of Basel, CH-4056Basel, Switzerland
B. Feja
Affiliation:
Biozentrum, M.E. Miiller Institute, University of Basel, CH-4056Basel, Switzerland
K. Goldie
Affiliation:
European Molecular Biology Laboratory, D-69117Heidelberg, Germany
Get access

Extract

The nuclear envelope (NE) physically separates the genetic machinery residing in the nucleus from protein synthesis taking place in the cytoplasm. Bidirectional transport of proteins, RNAs and RNP particles between these two compartments is mediated by the nuclear pore complexes (NPCs), large (-120 MDa) supramolecular assemblies embedded in the NE and being built of -100 different polypeptides, called nucleoporins. Extensive structural studies have revealed the 3D architecture of NPCs, and epitopes of several nucleoporins have been localized within their 3D structure.

In an attempt to go beyond the current consensus model of the NPC (Fig. lc, inset), we have embarked on a more systematic structural analysis of the molecular architecture of native NPCs. This is achieved by field-emission (FETEM; Fig. la) or energy-filtering (EFTEM; Fig. lb) TEM of completely unfixed and unstained Xenopus oocyte NEs embedded in thick (i.e. -200 nm) amorphous ice so that the 3D organization of the cytoplasmic and nuclear periphery of the NPCs (i.e. the cytoplasmic fibrils and nuclear baskets) is fully preserved (Fig. lb).

Type
Chambers and Channels: Functional Connections in Multiprotein Complexes Studied by Single Chambers and Channels
Information
Microscopy and Microanalysis , Volume 4 , Issue S2: Proceedings: Microscopy & Microanalysis '98, Microscopy Society of America 56th Annual Meeting, Microbeam Analysis Society 32nd Annual Meeting, Atlanta, Georgia July 12-16, 1998 , July 1998 , pp. 956 - 957
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

1.Pante, N. and Aebi, U., Curr. Opin. Cell Biol. 8(1996)397; Nigg, E., Nature 386(1997)779.CrossRefGoogle Scholar
2.Carafoli, E. et al., Cell Calcium 22(1997)313; Malviya, A. and Rogue, P., Cell 92(1998)17.CrossRefGoogle Scholar
3.Greber, U. and Gerace, L., J. Cell Biol. 128(1995)5.CrossRefGoogle Scholar
4.Perez-Terzic, et al., Science 273(1996)1875.CrossRefGoogle Scholar