Literature DB >> 12142286

Membrane fusion in eukaryotic cells.

Andreas Mayer1.   

Abstract

Membrane fusion is a fundamental biochemical reaction and the final step in all vesicular trafficking events. It is crucial for the transfer of proteins and lipids between different compartments and for exo- and endocytic traffic of signaling molecules and receptors. It leads to the reconstruction of organelles such as the Golgi or the nuclear envelope, which decay into fragments during mitosis. Hence, controlled membrane fusion reactions are indispensible for the compartmental organization of eukaryotic cells; for their communication with the environment via hormones, neurotransmitters, growth factors, and receptors; and for the integration of cells into multicellular organisms. Intracellular pathogenic bacteria, such as Mycobacteria or Salmonellae, have developed means to control fusion reactions in their host cells. They persist in phagosomes whose fusion with lysosomes they actively suppress-a means to ensure survival inside host cells. The past decade has witnessed rapid progress in the elucidation of parts of the molecular machinery involved in these membrane fusion reactions. Whereas some elements of the fusion apparatus are remarkably similar in several compartments, there is an equally striking divergence of others. The purpose of this review is to highlight common features of different fusion reactions and the concepts that emerged from them but also to stress the differences and challenge parts of the current hypotheses. This review covers only the endoplasmic fusion reactions mentioned above, i.e., reactions initiated by contacts of membranes with their cytoplasmic faces. Ectoplasmic fusion events, which depend on an initial contact of the fusion partners via the membrane surfaces exposed to the surrounding medium are not discussed, nor are topics such as the entry of enveloped viruses, formation of syncytia, gamete fusion, or vesicle scission (a fusion reaction that leads to the fission of, e.g., transport vesicles).

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Year:  2002        PMID: 12142286     DOI: 10.1146/annurev.cellbio.18.032202.114809

Source DB:  PubMed          Journal:  Annu Rev Cell Dev Biol        ISSN: 1081-0706            Impact factor:   13.827


  31 in total

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2.  Field theoretic study of bilayer membrane fusion: II. Mechanism of a stalk-hole complex.

Authors:  K Katsov; M Müller; M Schick
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3.  Molecular identification and reconstitution of depolarization-induced exocytosis monitored by membrane capacitance.

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4.  The ubiquitin-proteasome system regulates membrane fusion of yeast vacuoles.

Authors:  Maurits F Kleijnen; Donald S Kirkpatrick; Steven P Gygi
Journal:  EMBO J       Date:  2006-12-21       Impact factor: 11.598

5.  Transmembrane proteins are not required for early stages of nuclear envelope assembly.

Authors:  Corinne Ramos; Elvira R Rafikova; Kamran Melikov; Leonid V Chernomordik
Journal:  Biochem J       Date:  2006-12-15       Impact factor: 3.857

6.  Conformational changes of the HIV-1 envelope protein during membrane fusion are inhibited by the replacement of its membrane-spanning domain.

Authors:  Naoyuki Kondo; Kosuke Miyauchi; Fanxia Meng; Aikichi Iwamoto; Zene Matsuda
Journal:  J Biol Chem       Date:  2010-03-02       Impact factor: 5.157

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Authors:  Prit Lakhani; Akash Patil; Soumyajit Majumdar
Journal:  J Ocul Pharmacol Ther       Date:  2018-11-08       Impact factor: 2.671

8.  Enhanced membrane fusion in sterol-enriched vacuoles bypasses the Vrp1p requirement.

Authors:  Kelly Tedrick; Tim Trischuk; Richard Lehner; Gary Eitzen
Journal:  Mol Biol Cell       Date:  2004-07-14       Impact factor: 4.138

9.  A neuronal role for SNAP-23 in postsynaptic glutamate receptor trafficking.

Authors:  Young Ho Suh; Akira Terashima; Ronald S Petralia; Robert J Wenthold; John T R Isaac; Katherine W Roche; Paul A Roche
Journal:  Nat Neurosci       Date:  2010-01-31       Impact factor: 24.884

10.  Inner/Outer nuclear membrane fusion in nuclear pore assembly: biochemical demonstration and molecular analysis.

Authors:  Boris Fichtman; Corinne Ramos; Beth Rasala; Amnon Harel; Douglass J Forbes
Journal:  Mol Biol Cell       Date:  2010-10-06       Impact factor: 4.138

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