Mechanisms of enveloped virus entry into animal cells
Identifieur interne : 001196 ( Main/Exploration ); précédent : 001195; suivant : 001197Mechanisms of enveloped virus entry into animal cells
Auteurs : Per Johan Klasse [Royaume-Uni] ; Romke Bron [Royaume-Uni] ; Mark Marsh [Royaume-Uni]Source :
- Advanced Drug Delivery Reviews [ 0169-409X ] ; 1998.
English descriptors
- Teeft :
- Acad, Acidic, Actin, Adenovirus, Alphavirus, Alternative receptors, Biol, Boca raton, Bron, Capsid, Caveolae, Ccr5, Cell biol, Cell surface, Cell surface molecules, Cell surface receptors, Cellular, Cellular proteins, Chem, Chemokine, Chemokine receptor, Chemokine receptors, Choe, Conformational, Conformational change, Conformational changes, Cxcr4, Cytoplasmic, Dendritic cells, Different viruses, Drug delivery reviews, Embo, Endocytic, Endocytic organelles, Endocytic pathway, Endocytosis, Endoplasmic reticulum, Endosomal, Endosomes, Envelope glycoprotein, Envelope protein, Epitope, Fusion, Fusion peptide, Fusion peptides, Fusion protein, Fusion proteins, Fusogenic, Garoff, Glycoprotein, Golgi, Golgi apparatus, Haemagglutinin, Helenius, Helix, Hemagglutinin, Herpes, Herpes simplex virus, Histocompatibility, Human virus, Human virus type, Immunol, Internalised, Intracellular, Intracellular organelles, Kielian, Klasse, Late endosomes, Lentiviruses, Leukaemia, Ligand, Lipid, Lymphocyte, Lysosome, Macrophage, Macropinocytosis, Major histocompatibility, Membrane, Membrane fusion, Murine, Natl, Nucleocapsid, Organelle, Other viruses, Pathway, Peptide, Phagocytosis, Plasma membrane, Precursor, Primary receptor, Primate, Primate lentiviruses, Proc, Protease, Receptor, Receptor binding, Retroviral, Retroviridae, Retrovirus, Semliki, Semliki forest virus, Simian, Simian virus, Sindbis, Sindbis virus, Spike, Spike protein, Subunit, Target cell, Target membrane, Transmembrane, Transporter, Trends cell biol, Trimer, Trimeric, Vaccinia, Vesicle, Viral, Viral entry, Viral fusion mechanisms, Viral membrane, Virion, Virol, Virology, Virus, Virus assembly, Virus entry, Virus hemagglutinin, Virus infection, Virus particles, Virus receptors, Weiss, Wilschut.
Abstract
Abstract: The ability of viruses to transfer macromolecules between cells makes them attractive starting points for the design of biological delivery vehicles. Virus-based vectors and sub-viral systems are already finding biotechnological and medical applications for gene, peptide, vaccine and drug delivery. Progress has been made in understanding the cellular and molecular mechanisms underlying virus entry, particularly in identifying virus receptors. However, receptor binding is only a first step and we now have to understand how these molecules facilitate entry, how enveloped viruses fuse with cells or non-enveloped viruses penetrate the cell membrane, and what happens following penetration. Only through these detailed analyses will the full potential of viruses as vectors and delivery vehicles be realised. Here we discuss aspects of the entry mechanisms for several well-characterised viral systems. We do not attempt to provide a fully comprehensive review of virus entry but focus primarily on enveloped viruses.
Url:
DOI: 10.1016/S0169-409X(98)00002-7
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000919
- to stream Istex, to step Curation: 000897
- to stream Istex, to step Checkpoint: 000384
- to stream Main, to step Merge: 001209
- to stream Main, to step Curation: 001196
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title>Mechanisms of enveloped virus entry into animal cells</title><author><name sortKey="Klasse, Per Johan" sort="Klasse, Per Johan" uniqKey="Klasse P" first="Per Johan" last="Klasse">Per Johan Klasse</name></author><author><name sortKey="Bron, Romke" sort="Bron, Romke" uniqKey="Bron R" first="Romke" last="Bron">Romke Bron</name></author><author><name sortKey="Marsh, Mark" sort="Marsh, Mark" uniqKey="Marsh M" first="Mark" last="Marsh">Mark Marsh</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:3B57F1734B73725B582230F47B332A2B98B9D19B</idno><date when="1998" year="1998">1998</date><idno type="doi">10.1016/S0169-409X(98)00002-7</idno><idno type="url">https://api.istex.fr/ark:/67375/6H6-W9S00HX0-X/fulltext.pdf</idno><idno type="wicri:Area/Istex/Corpus">000919</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000919</idno><idno type="wicri:Area/Istex/Curation">000897</idno><idno type="wicri:Area/Istex/Checkpoint">000384</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000384</idno><idno type="wicri:doubleKey">0169-409X:1998:Klasse P:mechanisms:of:enveloped</idno><idno type="wicri:Area/Main/Merge">001209</idno><idno type="wicri:Area/Main/Curation">001196</idno><idno type="wicri:Area/Main/Exploration">001196</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a">Mechanisms of enveloped virus entry into animal cells</title><author><name sortKey="Klasse, Per Johan" sort="Klasse, Per Johan" uniqKey="Klasse P" first="Per Johan" last="Klasse">Per Johan Klasse</name><affiliation wicri:level="4"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Medical Research Council Laboratory for Molecular Cell Biology, and Department of Biochemistry and Molecular Biology, University College London, Gower Street, London WC1E 6BT</wicri:regionArea><orgName type="university">University College de Londres</orgName><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Bron, Romke" sort="Bron, Romke" uniqKey="Bron R" first="Romke" last="Bron">Romke Bron</name><affiliation wicri:level="4"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Medical Research Council Laboratory for Molecular Cell Biology, and Department of Biochemistry and Molecular Biology, University College London, Gower Street, London WC1E 6BT</wicri:regionArea><orgName type="university">University College de Londres</orgName><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author><author><name sortKey="Marsh, Mark" sort="Marsh, Mark" uniqKey="Marsh M" first="Mark" last="Marsh">Mark Marsh</name><affiliation wicri:level="4"><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Medical Research Council Laboratory for Molecular Cell Biology, and Department of Biochemistry and Molecular Biology, University College London, Gower Street, London WC1E 6BT</wicri:regionArea><orgName type="university">University College de Londres</orgName><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Advanced Drug Delivery Reviews</title><title level="j" type="abbrev">ADR</title><idno type="ISSN">0169-409X</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1998">1998</date><biblScope unit="volume">34</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="65">65</biblScope><biblScope unit="page" to="91">91</biblScope></imprint><idno type="ISSN">0169-409X</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0169-409X</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acad</term><term>Acidic</term><term>Actin</term><term>Adenovirus</term><term>Alphavirus</term><term>Alternative receptors</term><term>Biol</term><term>Boca raton</term><term>Bron</term><term>Capsid</term><term>Caveolae</term><term>Ccr5</term><term>Cell biol</term><term>Cell surface</term><term>Cell surface molecules</term><term>Cell surface receptors</term><term>Cellular</term><term>Cellular proteins</term><term>Chem</term><term>Chemokine</term><term>Chemokine receptor</term><term>Chemokine receptors</term><term>Choe</term><term>Conformational</term><term>Conformational change</term><term>Conformational changes</term><term>Cxcr4</term><term>Cytoplasmic</term><term>Dendritic cells</term><term>Different viruses</term><term>Drug delivery reviews</term><term>Embo</term><term>Endocytic</term><term>Endocytic organelles</term><term>Endocytic pathway</term><term>Endocytosis</term><term>Endoplasmic reticulum</term><term>Endosomal</term><term>Endosomes</term><term>Envelope glycoprotein</term><term>Envelope protein</term><term>Epitope</term><term>Fusion</term><term>Fusion peptide</term><term>Fusion peptides</term><term>Fusion protein</term><term>Fusion proteins</term><term>Fusogenic</term><term>Garoff</term><term>Glycoprotein</term><term>Golgi</term><term>Golgi apparatus</term><term>Haemagglutinin</term><term>Helenius</term><term>Helix</term><term>Hemagglutinin</term><term>Herpes</term><term>Herpes simplex virus</term><term>Histocompatibility</term><term>Human virus</term><term>Human virus type</term><term>Immunol</term><term>Internalised</term><term>Intracellular</term><term>Intracellular organelles</term><term>Kielian</term><term>Klasse</term><term>Late endosomes</term><term>Lentiviruses</term><term>Leukaemia</term><term>Ligand</term><term>Lipid</term><term>Lymphocyte</term><term>Lysosome</term><term>Macrophage</term><term>Macropinocytosis</term><term>Major histocompatibility</term><term>Membrane</term><term>Membrane fusion</term><term>Murine</term><term>Natl</term><term>Nucleocapsid</term><term>Organelle</term><term>Other viruses</term><term>Pathway</term><term>Peptide</term><term>Phagocytosis</term><term>Plasma membrane</term><term>Precursor</term><term>Primary receptor</term><term>Primate</term><term>Primate lentiviruses</term><term>Proc</term><term>Protease</term><term>Receptor</term><term>Receptor binding</term><term>Retroviral</term><term>Retroviridae</term><term>Retrovirus</term><term>Semliki</term><term>Semliki forest virus</term><term>Simian</term><term>Simian virus</term><term>Sindbis</term><term>Sindbis virus</term><term>Spike</term><term>Spike protein</term><term>Subunit</term><term>Target cell</term><term>Target membrane</term><term>Transmembrane</term><term>Transporter</term><term>Trends cell biol</term><term>Trimer</term><term>Trimeric</term><term>Vaccinia</term><term>Vesicle</term><term>Viral</term><term>Viral entry</term><term>Viral fusion mechanisms</term><term>Viral membrane</term><term>Virion</term><term>Virol</term><term>Virology</term><term>Virus</term><term>Virus assembly</term><term>Virus entry</term><term>Virus hemagglutinin</term><term>Virus infection</term><term>Virus particles</term><term>Virus receptors</term><term>Weiss</term><term>Wilschut</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: The ability of viruses to transfer macromolecules between cells makes them attractive starting points for the design of biological delivery vehicles. Virus-based vectors and sub-viral systems are already finding biotechnological and medical applications for gene, peptide, vaccine and drug delivery. Progress has been made in understanding the cellular and molecular mechanisms underlying virus entry, particularly in identifying virus receptors. However, receptor binding is only a first step and we now have to understand how these molecules facilitate entry, how enveloped viruses fuse with cells or non-enveloped viruses penetrate the cell membrane, and what happens following penetration. Only through these detailed analyses will the full potential of viruses as vectors and delivery vehicles be realised. Here we discuss aspects of the entry mechanisms for several well-characterised viral systems. We do not attempt to provide a fully comprehensive review of virus entry but focus primarily on enveloped viruses.</div></front></TEI><affiliations><list><country><li>Royaume-Uni</li></country><region><li>Angleterre</li><li>Grand Londres</li></region><settlement><li>Londres</li></settlement><orgName><li>University College de Londres</li></orgName></list><tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Klasse, Per Johan" sort="Klasse, Per Johan" uniqKey="Klasse P" first="Per Johan" last="Klasse">Per Johan Klasse</name></region><name sortKey="Bron, Romke" sort="Bron, Romke" uniqKey="Bron R" first="Romke" last="Bron">Romke Bron</name><name sortKey="Marsh, Mark" sort="Marsh, Mark" uniqKey="Marsh M" first="Mark" last="Marsh">Mark Marsh</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/CovidV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001196 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001196 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= CovidV1
|flux= Main
|étape= Exploration
|type= RBID
|clé= ISTEX:3B57F1734B73725B582230F47B332A2B98B9D19B
|texte= Mechanisms of enveloped virus entry into animal cells
}}
| This area was generated with Dilib version V0.6.33. |  |