Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.

We present a new antiviral strategy and research tool that could be applied to a wide range of enveloped viruses that infect human beings via membrane fusion. We test this strategy on two emerging zoonotic henipaviruses that cause fatal encephalitis in humans, Nipah (NiV) and Hendra (HeV) viruses. I...

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Main Authors: Matteo Porotto, Feng Yi, Anne Moscona, David A LaVan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-03-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0016874&type=printable
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author Matteo Porotto
Feng Yi
Anne Moscona
David A LaVan
author_facet Matteo Porotto
Feng Yi
Anne Moscona
David A LaVan
author_sort Matteo Porotto
collection DOAJ
description We present a new antiviral strategy and research tool that could be applied to a wide range of enveloped viruses that infect human beings via membrane fusion. We test this strategy on two emerging zoonotic henipaviruses that cause fatal encephalitis in humans, Nipah (NiV) and Hendra (HeV) viruses. In the new approach, artificial cell-like particles (protocells) presenting membrane receptors in a biomimetic manner were developed and found to attract and inactivate henipavirus envelope glycoprotein pseudovirus particles, preventing infection. The protocells do not accumulate virus during the inactivation process. The use of protocells that interact with, but do not accumulate, viruses may provide significant advantages over current antiviral drugs, and this general approach may have wide potential for antiviral development.
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institution DOAJ
issn 1932-6203
language English
publishDate 2011-03-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj-art-0ce33b43f717432b8d99e76b1da6570e2025-08-20T03:10:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-03-0163e1687410.1371/journal.pone.0016874Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.Matteo PorottoFeng YiAnne MosconaDavid A LaVanWe present a new antiviral strategy and research tool that could be applied to a wide range of enveloped viruses that infect human beings via membrane fusion. We test this strategy on two emerging zoonotic henipaviruses that cause fatal encephalitis in humans, Nipah (NiV) and Hendra (HeV) viruses. In the new approach, artificial cell-like particles (protocells) presenting membrane receptors in a biomimetic manner were developed and found to attract and inactivate henipavirus envelope glycoprotein pseudovirus particles, preventing infection. The protocells do not accumulate virus during the inactivation process. The use of protocells that interact with, but do not accumulate, viruses may provide significant advantages over current antiviral drugs, and this general approach may have wide potential for antiviral development.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0016874&type=printable
spellingShingle Matteo Porotto
Feng Yi
Anne Moscona
David A LaVan
Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.
PLoS ONE
title Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.
title_full Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.
title_fullStr Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.
title_full_unstemmed Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.
title_short Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.
title_sort synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0016874&type=printable
work_keys_str_mv AT matteoporotto syntheticprotocellsinteractwithviralnanomachineryandinactivatepathogenichumanvirus
AT fengyi syntheticprotocellsinteractwithviralnanomachineryandinactivatepathogenichumanvirus
AT annemoscona syntheticprotocellsinteractwithviralnanomachineryandinactivatepathogenichumanvirus
AT davidalavan syntheticprotocellsinteractwithviralnanomachineryandinactivatepathogenichumanvirus