Literature DB >> 6295454

Sendai virus membrane fusion: time course and effect of temperature, pH, calcium, and receptor concentration.

A M Haywood, B P Boyer.   

Abstract

The conditions that optimize Sendai virus membrane fusion with liposomes have been studied. No fusion occurs in the absence of ganglioside receptors. Maximum fusion occurs when the molar ratio of ganglioside GD1a to phospholipid is 0.02 or greater. The amount of fusion at 37 degrees C increases with time up to at least 6.5 h. The rate of fusion increases from the lowest temperature tested, 10 degrees C, to 40 degrees C. Above 43 degrees C the amount of fusion decreases because of thermal inactivation of the viral proteins. There is a broad pH maximum between pH 7.5 and pH 9.0. At both ends of the pH range the amount of fusion increases and exceeds that found in the physiologic pH range. Neither ethylenediaminetetraacetic acid nor Ca2+ changes the amount of membrane fusion. The optimal conditions for membrane fusion of Sendai virus membranes with liposomes are the same as the optimal conditions for fusion with host cells and with red blood cells. Since the liposomes contain no proteins, the optimal conditions for Sendai virus membrane fusion must be determined by the viral proteins and be mostly independent of the nature or presence of the host proteins.

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Year:  1982        PMID: 6295454     DOI: 10.1021/bi00267a003

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  15 in total

1.  Foamy virus envelope glycoprotein-mediated entry involves a pH-dependent fusion process.

Authors:  Marcus Picard-Maureau; Gergely Jarmy; Angelika Berg; Axel Rethwilm; Dirk Lindemann
Journal:  J Virol       Date:  2003-04       Impact factor: 5.103

2.  Effects of temperature on viral glycoprotein mobility and a possible role of internal "viroskeleton" proteins in Sendai virus fusion.

Authors:  S Ohki; H Thacore; T D Flanagan
Journal:  J Membr Biol       Date:  2004-05-15       Impact factor: 1.843

3.  Early Viral Entry Assays for the Identification and Evaluation of Antiviral Compounds.

Authors:  Chen-Jei Tai; Chia-Lin Li; Cheng-Jeng Tai; Chien-Kai Wang; Liang-Tzung Lin
Journal:  J Vis Exp       Date:  2015-10-29       Impact factor: 1.355

4.  Permeability changes resulting from virus-cell fusion: temperature-dependence of the contributing processes.

Authors:  K J Micklem; A Nyaruwe; C A Pasternak
Journal:  Mol Cell Biochem       Date:  1985-03       Impact factor: 3.396

5.  Sendai virus-erythrocyte membrane interaction: quantitative and kinetic analysis of viral binding, dissociation, and fusion.

Authors:  D Hoekstra; K Klappe
Journal:  J Virol       Date:  1986-04       Impact factor: 5.103

6.  Role of glycosphingolipid microdomains in CD4-dependent HIV-1 fusion.

Authors:  J Fantini; D Hammache; G Piéroni; N Yahi
Journal:  Glycoconj J       Date:  2000 Mar-Apr       Impact factor: 2.916

Review 7.  Virus receptors: binding, adhesion strengthening, and changes in viral structure.

Authors:  A M Haywood
Journal:  J Virol       Date:  1994-01       Impact factor: 5.103

8.  Electric pulse-induced fusion of mouse lymphoma cells: roles of divalent cations and membrane lipid domains.

Authors:  T Ohno-Shosaku; Y Okada
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

9.  Characteristics of fusion of respiratory syncytial virus with HEp-2 cells as measured by R18 fluorescence dequenching assay.

Authors:  N Srinivasakumar; P L Ogra; T D Flanagan
Journal:  J Virol       Date:  1991-08       Impact factor: 5.103

10.  Influence of calcium on lipid mixing mediated by influenza hemagglutinin.

Authors:  Mikhail A Zhukovsky; Ingrid Markovic; Austin L Bailey
Journal:  Arch Biochem Biophys       Date:  2007-05-25       Impact factor: 4.013

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