Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development

Membrane-enveloped viruses are responsible for most viral pandemics in history, and more effort is needed to advance broadly applicable countermeasures to mitigate the impact of future outbreaks. In this Perspective, we discuss how biosensing techniques associated with lipid model membrane platforms...

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Main Authors: Park, Soohyun, Cho, Nam-Joon
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/168945
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1689452023-06-23T05:25:41Z Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development Park, Soohyun Cho, Nam-Joon School of Materials Science and Engineering Engineering::Materials Antimicrobial Agents Membranes Membrane-enveloped viruses are responsible for most viral pandemics in history, and more effort is needed to advance broadly applicable countermeasures to mitigate the impact of future outbreaks. In this Perspective, we discuss how biosensing techniques associated with lipid model membrane platforms are contributing to improving our mechanistic knowledge of membrane fusion and destabilization that is closely linked to viral entry as well as vaccine and antiviral drug development. A key benefit of these platforms is the simplicity of interpreting the results which can be complemented by other techniques to decipher more complicated biological observations and evaluate the biophysical functionalities that can be correlated to biological activities. Then, we introduce exciting application examples of membrane-targeting antivirals that have been refined over time and will continue to improve based on biophysical insights. Two ways to abrogate the function of viral membranes are introduced here: (1) selective disruption of the viral membrane structure and (2) alteration of the membrane component. While both methods are suitable for broadly useful antivirals, the latter also has the potential to produce an inactivated vaccine. Collectively, we emphasize how biosensing tools based on membrane interfacial science can provide valuable information that could be translated into biomedicines and improve their selectivity and performance. Ministry of Education (MOE) This work was supported by the Ministry of Education (MOE) in Singapore under grant RG111/20 and by a sponsored research agreement from LUCA AICell Inc. (RCA-LUCA AICell REQ0239282). 2023-06-23T05:24:28Z 2023-06-23T05:24:28Z 2023 Journal Article Park, S. & Cho, N. (2023). Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development. Langmuir, 39(1), 1-11. https://dx.doi.org/10.1021/acs.langmuir.2c02501 0743-7463 https://hdl.handle.net/10356/168945 10.1021/acs.langmuir.2c02501 36576966 2-s2.0-85145471074 1 39 1 11 en RG111/20 Langmuir © 2022 American Chemical Society. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials
Antimicrobial Agents
Membranes
spellingShingle Engineering::Materials
Antimicrobial Agents
Membranes
Park, Soohyun
Cho, Nam-Joon
Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
description Membrane-enveloped viruses are responsible for most viral pandemics in history, and more effort is needed to advance broadly applicable countermeasures to mitigate the impact of future outbreaks. In this Perspective, we discuss how biosensing techniques associated with lipid model membrane platforms are contributing to improving our mechanistic knowledge of membrane fusion and destabilization that is closely linked to viral entry as well as vaccine and antiviral drug development. A key benefit of these platforms is the simplicity of interpreting the results which can be complemented by other techniques to decipher more complicated biological observations and evaluate the biophysical functionalities that can be correlated to biological activities. Then, we introduce exciting application examples of membrane-targeting antivirals that have been refined over time and will continue to improve based on biophysical insights. Two ways to abrogate the function of viral membranes are introduced here: (1) selective disruption of the viral membrane structure and (2) alteration of the membrane component. While both methods are suitable for broadly useful antivirals, the latter also has the potential to produce an inactivated vaccine. Collectively, we emphasize how biosensing tools based on membrane interfacial science can provide valuable information that could be translated into biomedicines and improve their selectivity and performance.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Park, Soohyun
Cho, Nam-Joon
format Article
author Park, Soohyun
Cho, Nam-Joon
author_sort Park, Soohyun
title Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
title_short Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
title_full Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
title_fullStr Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
title_full_unstemmed Lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
title_sort lipid membrane interface viewpoint: from viral entry to antiviral and vaccine development
publishDate 2023
url https://hdl.handle.net/10356/168945
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