Surface ultrastructure of SARS coronavirus revealed by atomic force microscopy.
Identifieur interne : 002431 ( PubMed/Curation ); précédent : 002430; suivant : 002432Surface ultrastructure of SARS coronavirus revealed by atomic force microscopy.
Auteurs : Shiming Lin [Taïwan] ; Chih-Kung Lee ; Shih-Yuan Lee ; Chuan-Liang Kao ; Chii-Wann Lin ; An-Bang Wang ; Su-Ming Hsu ; Long-Sun HuangSource :
- Cellular microbiology [ 1462-5814 ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , ultrastructure : Hemagglutinins, Viral, Membrane Glycoproteins, Viral Envelope Proteins.
- chemistry : SARS Virus.
- ultrastructure : SARS Virus, Virion.
- Microscopy, Atomic Force, Spike Glycoprotein, Coronavirus.
Abstract
Atomic force microscopy has been used to probe the surface nanostructures of severe acute respiratory syndrome coronavirus (SARS-CoV). Single crown-like virion was directly visualized and quantitative measurements of the dimensions for the structural proteins were provided. A corona of large, distinctive spikes in the envelope was measured after treatment with hydroxyoctanoic acid. High-resolution images revealed that the surface of each single SARS-CoV was surrounded with at least 15 spherical spikes having a diameter of 7.29 +/- 0.73 nm, which is in close agreement with that of S glycoproteins earlier predicted through the genomes of SARS-CoV. This study represents the first direct characterization of the surface ultrastructures of SARS-CoV particles at the nanometre scale and offers new prospects for mapping viral surface properties.
DOI: 10.1111/j.1462-5822.2005.00593.x
PubMed: 16309462
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<author><name sortKey="Wang, An Bang" sort="Wang, An Bang" uniqKey="Wang A" first="An-Bang" last="Wang">An-Bang Wang</name>
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<term>Microscopy, Atomic Force</term>
<term>SARS Virus (chemistry)</term>
<term>SARS Virus (ultrastructure)</term>
<term>Spike Glycoprotein, Coronavirus</term>
<term>Viral Envelope Proteins (ultrastructure)</term>
<term>Virion (ultrastructure)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Glycoprotéine de spicule des coronavirus</term>
<term>Glycoprotéines membranaires (ultrastructure)</term>
<term>Hémagglutinines virales (ultrastructure)</term>
<term>Microscopie à force atomique</term>
<term>Protéines de l'enveloppe virale (ultrastructure)</term>
<term>Virion (ultrastructure)</term>
<term>Virus du SRAS ()</term>
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<front><div type="abstract" xml:lang="en">Atomic force microscopy has been used to probe the surface nanostructures of severe acute respiratory syndrome coronavirus (SARS-CoV). Single crown-like virion was directly visualized and quantitative measurements of the dimensions for the structural proteins were provided. A corona of large, distinctive spikes in the envelope was measured after treatment with hydroxyoctanoic acid. High-resolution images revealed that the surface of each single SARS-CoV was surrounded with at least 15 spherical spikes having a diameter of 7.29 +/- 0.73 nm, which is in close agreement with that of S glycoproteins earlier predicted through the genomes of SARS-CoV. This study represents the first direct characterization of the surface ultrastructures of SARS-CoV particles at the nanometre scale and offers new prospects for mapping viral surface properties.</div>
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<Abstract><AbstractText>Atomic force microscopy has been used to probe the surface nanostructures of severe acute respiratory syndrome coronavirus (SARS-CoV). Single crown-like virion was directly visualized and quantitative measurements of the dimensions for the structural proteins were provided. A corona of large, distinctive spikes in the envelope was measured after treatment with hydroxyoctanoic acid. High-resolution images revealed that the surface of each single SARS-CoV was surrounded with at least 15 spherical spikes having a diameter of 7.29 +/- 0.73 nm, which is in close agreement with that of S glycoproteins earlier predicted through the genomes of SARS-CoV. This study represents the first direct characterization of the surface ultrastructures of SARS-CoV particles at the nanometre scale and offers new prospects for mapping viral surface properties.</AbstractText>
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