Micropatterned viral membrane clusters for antiviral drug evaluation
The function of biological nanoparticles, such as membrane-enveloped viral particles, is often enhanced when the particles form higher-order supramolecular assemblies. While there is intense interest in developing biomimetic platforms that recapitulate these collective properties, existing platforms...
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sg-ntu-dr.10356-1513742022-07-22T08:21:44Z Micropatterned viral membrane clusters for antiviral drug evaluation Park, Soohyun Jackman, Joshua A. Xu, Xiaobin Weiss, Paul S. Cho, Nam-Joon School of Materials Science and Engineering School of Chemical and Biomedical Engineering Engineering::Materials Micropatterning Nanotechnology The function of biological nanoparticles, such as membrane-enveloped viral particles, is often enhanced when the particles form higher-order supramolecular assemblies. While there is intense interest in developing biomimetic platforms that recapitulate these collective properties, existing platforms are limited to mimicking individual virus particles. Here, we present a micropatterning strategy to print linker molecules selectively onto bioinert surfaces, thereby enabling controlled tethering of biomimetic viral particle clusters across defined geometric patterns. By controlling the linker concentration, it is possible to tune the density of tethered particles within clusters while enhancing the signal intensity of encapsulated fluorescent markers. Time-resolved tracking of pore formation and membrane lysis revealed that an antiviral peptide can disturb clusters of the membrane-enclosed particles akin to the targeting of individual viral particles. This platform is broadly useful for evaluating the performance of membrane-active antiviral drug candidates, whereas the micropatterning strategy can be applied to a wide range of biological nanoparticles and other macromolecular entities. National Research Foundation (NRF) This work was supported by the National Research Foundation of Singapore through a Competitive Research Programme grant (NRF-CRP10-2012-07) and a Proof-of-Concept grant (NRF2015NRF-POC0001-19). Additional support was provided by the Creative Materials Discovery Program through the National Research Foundation of Korea funded by the Ministry of Science, ICT and Future Planning (NRF-2016M3D1A1024098). The fabrication was supported by a (US) National Science Foundation Nanomanufacturing grant #CMMI-1636136. 2021-07-23T09:32:09Z 2021-07-23T09:32:09Z 2019 Journal Article Park, S., Jackman, J. A., Xu, X., Weiss, P. S. & Cho, N. (2019). Micropatterned viral membrane clusters for antiviral drug evaluation. ACS Applied Materials and Interfaces, 11(15), 13984-13990. https://dx.doi.org/10.1021/acsami.9b01724 1944-8244 0000-0003-3261-7585 0000-0002-1800-8102 0000-0002-3479-0130 0000-0001-5527-6248 0000-0002-8692-8955 https://hdl.handle.net/10356/151374 10.1021/acsami.9b01724 30855935 2-s2.0-85064344936 15 11 13984 13990 en NRF-CRP10-2012-07 NRF2015NRF-POC0001-19 ACS Applied Materials and Interfaces © 2019 American Chemical Society. All rights reserved. |
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Engineering::Materials Micropatterning Nanotechnology Park, Soohyun Jackman, Joshua A. Xu, Xiaobin Weiss, Paul S. Cho, Nam-Joon Micropatterned viral membrane clusters for antiviral drug evaluation |
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The function of biological nanoparticles, such as membrane-enveloped viral particles, is often enhanced when the particles form higher-order supramolecular assemblies. While there is intense interest in developing biomimetic platforms that recapitulate these collective properties, existing platforms are limited to mimicking individual virus particles. Here, we present a micropatterning strategy to print linker molecules selectively onto bioinert surfaces, thereby enabling controlled tethering of biomimetic viral particle clusters across defined geometric patterns. By controlling the linker concentration, it is possible to tune the density of tethered particles within clusters while enhancing the signal intensity of encapsulated fluorescent markers. Time-resolved tracking of pore formation and membrane lysis revealed that an antiviral peptide can disturb clusters of the membrane-enclosed particles akin to the targeting of individual viral particles. This platform is broadly useful for evaluating the performance of membrane-active antiviral drug candidates, whereas the micropatterning strategy can be applied to a wide range of biological nanoparticles and other macromolecular entities. |
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School of Materials Science and Engineering |
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School of Materials Science and Engineering Park, Soohyun Jackman, Joshua A. Xu, Xiaobin Weiss, Paul S. Cho, Nam-Joon |
format |
Article |
author |
Park, Soohyun Jackman, Joshua A. Xu, Xiaobin Weiss, Paul S. Cho, Nam-Joon |
author_sort |
Park, Soohyun |
title |
Micropatterned viral membrane clusters for antiviral drug evaluation |
title_short |
Micropatterned viral membrane clusters for antiviral drug evaluation |
title_full |
Micropatterned viral membrane clusters for antiviral drug evaluation |
title_fullStr |
Micropatterned viral membrane clusters for antiviral drug evaluation |
title_full_unstemmed |
Micropatterned viral membrane clusters for antiviral drug evaluation |
title_sort |
micropatterned viral membrane clusters for antiviral drug evaluation |
publishDate |
2021 |
url |
https://hdl.handle.net/10356/151374 |
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1739837455571353600 |