Literature DB >> 28579449

Structural dynamics of the nuclear pore complex.

Yusuke Sakiyama1, Radhakrishnan Panatala1, Roderick Y H Lim2.   

Abstract

Nuclear pore complexes (NPCs) are the sole conduits that facilitate macromolecular exchange between the nucleus and cytosol. Recent advancements have led to a more highly resolved NPC structure. However, our understanding of the NPC modus operandi that facilitates transport selectivity, and speed, of diverse cargoes remains incomplete. For the most part, assorted cargo-complexes of different sizes traverse the NPC central channel in milliseconds, yet little is known about the nanoscopic movements of its barrier-forming Phe-Gly nucleoporins (FG Nups) and related sub-structures at transport-relevant time and length scales. Here, we discuss how dynamic FG Nup behavior may confer NPCs with an effective permeability barrier according to the functional needs of the cell. Moreover, we postulate that structural flexibility might resonate throughout the NPC framework from the cytoplasmic filaments to the nuclear basket.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  High-speed atomic force microscopy; Intrinsically disordered proteins; Nuclear basket; Nuclear pore complex; Nucleoporin; Structural dynamics

Mesh:

Substances:

Year:  2017        PMID: 28579449     DOI: 10.1016/j.semcdb.2017.05.021

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  10 in total

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5.  Physics of the Nuclear Pore Complex: Theory, Modeling and Experiment.

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6.  Molecular interactions of FG nucleoporin repeats at high resolution.

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Review 7.  One Ring to Rule them All? Structural and Functional Diversity in the Nuclear Pore Complex.

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Review 8.  On the nuclear pore complex and its emerging role in cellular mechanotransduction.

Authors:  Atsushi Matsuda; Mohammad R K Mofrad
Journal:  APL Bioeng       Date:  2022-03-10

Review 9.  Mechanisms of nuclear pore complex assembly - two different ways of building one molecular machine.

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  10 in total

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