Literature DB >> 11498040

Influenza fusion peptides.

J J Skehel1, K Cross, D Steinhauer, D C Wiley.   

Abstract

The 'fusion peptides' of a group of enveloped viruses that includes influenza, paramyxo-, retro-and filo-viruses are N-terminal regions of their membrane fusion proteins generated by cleavage of non-functional precursors. For the influenza membrane fusion protein, haemagglutinin (HA), the three-dimensional structures of precursor HA, cleaved HA and fusion-activated HA show that the fusion peptides are located in different positions in all three forms and adopt different structures. Analyses of mutant HAs with changes in fusion peptide sequence indicate the importance of specific residues for membrane-fusion activity and suggest a structure for the fusion peptide in a fusion-active molecule.

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Year:  2001        PMID: 11498040     DOI: 10.1042/bst0290623

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  19 in total

1.  Unusual topological arrangement of structural motifs in the baboon reovirus fusion-associated small transmembrane protein.

Authors:  Sandra Dawe; Jennifer A Corcoran; Eileen K Clancy; Jayme Salsman; Roy Duncan
Journal:  J Virol       Date:  2005-05       Impact factor: 5.103

2.  Spring-loaded heptad repeat residues regulate the expression and activation of paramyxovirus fusion protein.

Authors:  Laura E Luque; Charles J Russell
Journal:  J Virol       Date:  2007-01-24       Impact factor: 5.103

3.  Substrate filtering by the active site crossover loop in UCHL3 revealed by sortagging and gain-of-function mutations.

Authors:  Maximilian W Popp; Katerina Artavanis-Tsakonas; Hidde L Ploegh
Journal:  J Biol Chem       Date:  2008-12-01       Impact factor: 5.157

4.  Phospholipase D facilitates efficient entry of influenza virus, allowing escape from innate immune inhibition.

Authors:  Thomas H Oguin; Shalini Sharma; Amanda D Stuart; Susu Duan; Sarah A Scott; Carrie K Jones; J Scott Daniels; Craig W Lindsley; Paul G Thomas; H Alex Brown
Journal:  J Biol Chem       Date:  2014-07-27       Impact factor: 5.157

5.  The presence of a single N-terminal histidine residue enhances the fusogenic properties of a Membranotropic peptide derived from herpes simplex virus type 1 glycoprotein H.

Authors:  Stefania Galdiero; Annarita Falanga; Mariateresa Vitiello; Luca Raiola; Luigi Russo; Carlo Pedone; Carla Isernia; Massimiliano Galdiero
Journal:  J Biol Chem       Date:  2010-03-26       Impact factor: 5.157

6.  The Atlastin C-terminal tail is an amphipathic helix that perturbs the bilayer structure during endoplasmic reticulum homotypic fusion.

Authors:  Joseph E Faust; Tanvi Desai; Avani Verma; Idil Ulengin; Tzu-Lin Sun; Tyler J Moss; Miguel A Betancourt-Solis; Huey W Huang; Tina Lee; James A McNew
Journal:  J Biol Chem       Date:  2015-01-02       Impact factor: 5.157

Review 7.  Technologies for investigating the physiological barriers to efficient lipid nanoparticle-siRNA delivery.

Authors:  Bin Shi; Marc Abrams
Journal:  J Histochem Cytochem       Date:  2013-03-14       Impact factor: 2.479

8.  Atypical fusion peptide of Nelson Bay virus fusion-associated small transmembrane protein.

Authors:  LiTing T Cheng; Richard K Plemper; Richard W Compans
Journal:  J Virol       Date:  2005-02       Impact factor: 5.103

9.  Hemagglutinin homologue from H17N10 bat influenza virus exhibits divergent receptor-binding and pH-dependent fusion activities.

Authors:  Xueyong Zhu; Wenli Yu; Ryan McBride; Yan Li; Li-Mei Chen; Ruben O Donis; Suxiang Tong; James C Paulson; Ian A Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-07       Impact factor: 11.205

10.  Comparative study on transduction and toxicity of protein transduction domains.

Authors:  T Sugita; T Yoshikawa; Y Mukai; N Yamanada; S Imai; K Nagano; Y Yoshida; H Shibata; Y Yoshioka; S Nakagawa; H Kamada; S-I Tsunoda; Y Tsutsumi
Journal:  Br J Pharmacol       Date:  2008-01-28       Impact factor: 8.739

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