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), plaque, RT-qPCR, and immunofluorescence assays, while maintaining >90% cell viability. These nanosheets significantly reduced infectious titers, viral RNA replication, and intracellular viral protein expression, indicating inhibition at early stages of viral entry and propagation. The sequence programmability, chemical robustness, and mutation-insensitive antiviral activity distinguish 2DNMs from traditional antivirals and position them as a versatile material platform for antiviral coatings, protective barriers, and prophylactic biomedical applications.
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Baylie Phillips
Thi Kim Hoang Trinh
Jacob Beitzel
ACS Nano
University of Washington
Pacific Northwest National Laboratory
Physical Sciences (United States)
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Phillips et al. (Wed,) studied this question.
www.synapsesocial.com/papers/6a08093ca487c87a6a40b307 — DOI: https://doi.org/10.1021/acsnano.6c04885