Filamentous anti-influenza agents wrapping around viruses

Jinhyo Chung, Younghun Jung, Caleb Hong, Subin Kim, Seokoh Moon, Eun A. Kwak, Beom Jeung Hwang, Seong Hyun Park, Baik Lin Seong, Dae Hyuk Kweon, Woo Jae Chung

Research output: Contribution to journalArticlepeer-review

Abstract

Owing to the emerging resistance to current anti-influenza therapies, strategies for blocking virus–cell interaction with agents that mimic interactions with host cell receptors are garnering interest. In this context, a multivalent presentation of sialyl groups on various types of scaffold materials such as dendrimers, liposomes, nanoparticles, and natural/synthetic polymers has been investigated for the inhibition of influenza A virus infection. However, the development of versatile antiviral agents based on monodisperse scaffolds capable of precise molecular design remains challenging. Whether an anisotropically extended filamentous nanostructure can serve as an effective scaffold for maximum inhibition of viral cell attachment has not been investigated. In this study, the preparation of a series of sialyllactose-conjugated filamentous bacteriophages (SLPhages), with controlled loading levels, ligand valencies, and two types of sialyllactose (α2,3′ and α2,6′), is demonstrated. With optimal ligand loading and valency, SLPhages showed inhibitory activity (in vitro) against influenza A viruses at concentrations of tens of picomolar. This remarkable inhibition is due to the strong interaction between the SLPhage and the virus; this interaction is adequately potent to compensate for the cost of the bending and wrapping of the SLPhage around the influenza virus. Our study may open new avenues for the development of filamentous anti-viral agents, in which virus-wrapping or aggregation is the primary feature responsible for the blocking of cell entry.

Original languageEnglish
Pages (from-to)267-278
Number of pages12
JournalJournal of Colloid and Interface Science
Volume583
DOIs
Publication statusPublished - 2021 Feb 1

Bibliographical note

Funding Information:
This research was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MIST) (No. 2019R1A2C1006856 ). This research was also partially supported by the National Research Foundation of Korea (NRF) funded by the Ministry of Education ( 2017R1A6A1A03015642 ) and by the Ministry of Science, ICT and Future Planning ( NRF-2016M3A7B4909581 ).

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Biomaterials
  • Surfaces, Coatings and Films
  • Colloid and Surface Chemistry

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