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About:
Crystal Structure of the Hendra Virus Attachment G Glycoprotein Bound to a Potent Cross-Reactive Neutralizing Human Monoclonal Antibody
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An Entity of Type :
schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Crystal Structure of the Hendra Virus Attachment G Glycoprotein Bound to a Potent Cross-Reactive Neutralizing Human Monoclonal Antibody
Creator
Chan, Yee-Peng
Zhu, Zhongyu
Feldmann, Heinz
Xu, Yan
Rockx, Barry
Xu, Kai
Bishop-Lilly, Kimberly
Broder, Christopher
Debuysscher, Blair
Dimitrov, Dimiter
Mokashi, Vishwesh
Cer, Regina
Fusco, Deborah
Luu, Truong
Nikolov, Dimitar
Xie, Yihu
Source
Medline; PMC
abstract
The henipaviruses, represented by Hendra (HeV) and Nipah (NiV) viruses are highly pathogenic zoonotic paramyxoviruses with uniquely broad host tropisms responsible for repeated outbreaks in Australia, Southeast Asia, India and Bangladesh. The high morbidity and mortality rates associated with infection and lack of licensed antiviral therapies make the henipaviruses a potential biological threat to humans and livestock. Henipavirus entry is initiated by the attachment of the G envelope glycoprotein to host cell membrane receptors. Previously, henipavirus-neutralizing human monoclonal antibodies (hmAb) have been isolated using the HeV-G glycoprotein and a human naïve antibody library. One cross-reactive and receptor-blocking hmAb (m102.4) was recently demonstrated to be an effective post-exposure therapy in two animal models of NiV and HeV infection, has been used in several people on a compassionate use basis, and is currently in development for use in humans. Here, we report the crystal structure of the complex of HeV-G with m102.3, an m102.4 derivative, and describe NiV and HeV escape mutants. This structure provides detailed insight into the mechanism of HeV and NiV neutralization by m102.4, and serves as a blueprint for further optimization of m102.4 as a therapeutic agent and for the development of entry inhibitors and vaccines.
has issue date
2013-10-10
(
xsd:dateTime
)
bibo:doi
10.1371/journal.ppat.1003684
bibo:pmid
24130486
has license
cc0
sha1sum (hex)
7dbdecefcd59460800cc11324be0595779ffde80
schema:url
https://doi.org/10.1371/journal.ppat.1003684
resource representing a document's title
Crystal Structure of the Hendra Virus Attachment G Glycoprotein Bound to a Potent Cross-Reactive Neutralizing Human Monoclonal Antibody
has PubMed Central identifier
PMC3795035
has PubMed identifier
24130486
schema:publication
PLoS Pathog
resource representing a document's body
covid:7dbdecefcd59460800cc11324be0595779ffde80#body_text
is
schema:about
of
named entity 'G GLYCOPROTEIN'
named entity 'Bangladesh'
named entity 'animal models'
named entity 'potential'
named entity 'human'
named entity 'envelope'
named entity 'therapy'
named entity 'crystal structure'
named entity 'therapies'
named entity 'describe'
named entity 'Antibody'
named entity 'LICENSED'
named entity 'OUTBREAKS'
named entity 'ATTACHMENT'
named entity 'DESCRIBE'
named entity 'DERIVATIVE'
named entity 'ASSOCIATED WITH'
named entity 'COMPASSIONATE USE'
named entity 'MUTANTS'
named entity 'ESCAPE'
named entity 'USE'
named entity 'HENDRA VIRUS'
named entity 'MONOCLONAL ANTIBODY'
named entity 'INFECTION'
named entity 'REPEATED'
named entity 'THERAPEUTIC AGENT'
named entity 'PARAMYXOVIRUSES'
named entity 'THERAPIES'
named entity 'USING'
named entity 'HENIPAVIRUSES'
named entity 'CURRENTLY'
named entity 'HEV'
named entity 'MEMBRANE RECEPTORS'
named entity 'DEMONSTRATED'
named entity 'BROAD'
named entity 'ANTIBODY LIBRARY'
named entity 'EXPOSURE THERAPY'
named entity 'VIRUS ATTACHMENT'
named entity 'HOST'
named entity 'ANIMAL MODELS '
named entity 'CRYSTAL STRUCTURE'
named entity 'EFFECTIVE'
named entity 'CROSS-REACTIVE'
named entity 'CRYSTAL STRUCTURE'
named entity 'BOUND'
named entity 'HUMAN'
named entity 'COMPLEX'
named entity 'HUMANS'
named entity 'BLOCKING'
named entity 'MONOCLONAL ANTIBODIES'
named entity 'PROVIDES'
named entity 'PATHOGENIC'
named entity 'TROPISMS'
named entity 'HIGHLY'
named entity 'NIV'
named entity 'HERE'
named entity 'INSIGHT'
named entity 'MECHANISM'
named entity 'ANTIVIRAL'
named entity 'PEOPLE'
named entity 'ENTRY'
named entity 'USED'
named entity 'DETAILED'
named entity 'AUSTRALIA'
named entity 'MORBIDITY AND MORTALITY'
named entity 'VACCINES'
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