Solid-to-fluid–like DNA transition in viruses facilitates infection
Identifieur interne : 001240 ( Main/Exploration ); précédent : 001239; suivant : 001241Solid-to-fluid–like DNA transition in viruses facilitates infection
Auteurs : Ting Liu ; Udom Sae-Ueng ; Dong Li ; Gabriel C. Lander ; Xiaobing Zuo ; Bengt Jönsson [Suède] ; Donald Rau ; Ivetta Shefer ; Alex Evilevitch [Suède]Source :
- Proceedings of the National Academy of Sciences of the United States of America [ 0027-8424 ] ; 2014.
Descripteurs français
- KwdFr :
- ADN viral (), ADN viral (ultrastructure), Bactériophage lambda (), Bactériophage lambda (ultrastructure), Capside (), Cinétique, Cryomicroscopie électronique, Escherichia coli (virologie), Fluorescence, Humains, Maladies virales (virologie), Microscopie à force atomique, Thermodynamique, Transition de phase.
- MESH :
English descriptors
- KwdEn :
- Bacteriophage lambda (chemistry), Bacteriophage lambda (ultrastructure), Capsid (chemistry), Cryoelectron Microscopy, DNA, Viral (chemistry), DNA, Viral (ultrastructure), Escherichia coli (virology), Fluorescence, Humans, Kinetics, Microscopy, Atomic Force, Phase Transition, Thermodynamics, Virus Diseases (virology).
- MESH :
- chemical , chemistry : DNA, Viral.
- chemistry : Bacteriophage lambda, Capsid.
- ultrastructure : Bacteriophage lambda, DNA, Viral.
- virology : Escherichia coli, Virus Diseases.
- Cryoelectron Microscopy, Fluorescence, Humans, Kinetics, Microscopy, Atomic Force, Phase Transition, Thermodynamics.
Abstract
The efficiency of viral replication is limited by the ability of the virus to eject its genome into a cell. We discovered a fundamentally important mechanism for translocation of viral genomes into cells. For the first time, to our knowledge, we show that tightly packaged DNA in the viral capsid of a bacterial virus (phage λ) undergoes a solid-to-fluid–like structural transition that facilitates infection close to 37 °C. Our finding shows a remarkable physical adaptation of bacterial viruses to the environment of
Url:
DOI: 10.1073/pnas.1321637111
PubMed: 25271319
PubMed Central: 4205597
Affiliations:
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Le document en format XML
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<term>Capsid (chemistry)</term>
<term>Cryoelectron Microscopy</term>
<term>DNA, Viral (chemistry)</term>
<term>DNA, Viral (ultrastructure)</term>
<term>Escherichia coli (virology)</term>
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<term>Humans</term>
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<term>Thermodynamics</term>
<term>Virus Diseases (virology)</term>
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<term>ADN viral (ultrastructure)</term>
<term>Bactériophage lambda ()</term>
<term>Bactériophage lambda (ultrastructure)</term>
<term>Capside ()</term>
<term>Cinétique</term>
<term>Cryomicroscopie électronique</term>
<term>Escherichia coli (virologie)</term>
<term>Fluorescence</term>
<term>Humains</term>
<term>Maladies virales (virologie)</term>
<term>Microscopie à force atomique</term>
<term>Thermodynamique</term>
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<term>Cryomicroscopie électronique</term>
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<front><div type="abstract" xml:lang="en"><title>Significance</title>
<p>The efficiency of viral replication is limited by the ability of the virus to eject its genome into a cell. We discovered a fundamentally important mechanism for translocation of viral genomes into cells. For the first time, to our knowledge, we show that tightly packaged DNA in the viral capsid of a bacterial virus (phage λ) undergoes a solid-to-fluid–like structural transition that facilitates infection close to 37 °C. Our finding shows a remarkable physical adaptation of bacterial viruses to the environment of <italic>Escherichia coli</italic>
cells in a human host.</p>
</div>
</front>
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<name sortKey="Liu, Ting" sort="Liu, Ting" uniqKey="Liu T" first="Ting" last="Liu">Ting Liu</name>
<name sortKey="Rau, Donald" sort="Rau, Donald" uniqKey="Rau D" first="Donald" last="Rau">Donald Rau</name>
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<name sortKey="Zuo, Xiaobing" sort="Zuo, Xiaobing" uniqKey="Zuo X" first="Xiaobing" last="Zuo">Xiaobing Zuo</name>
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