Design and Functional Analysis of Heterobifunctional Multivalent Phage Capsid Inhibitors Blocking the Entry of Influenza Virus-Reference-Cited by-同舟云学术

Design and Functional Analysis of Heterobifunctional Multivalent Phage Capsid Inhibitors Blocking the Entry of Influenza Virus

Published:2022-06-27 Issue:7 Volume:33 Page:1269-1278
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Adam Lutz¹²^ORCID,Müller Eva³,Ludwig Kai⁴,Klenk Simon¹²,Lauster Daniel⁵,Liese Susanne⁶⁷,Herrmann Andreas⁵,Hackenberger Christian P. R.¹²^ORCID

Affiliation:

1. Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Rössle-Straße 10, 13125 Berlin, Germany

2. Institut für Chemie, Humboldt-Universität zu Berlin, Brook-Taylor-Street 2, 12489 Berlin, Germany

3. Institut für translationale HIV Forschung, Universitätsklinikum Essen, Virchowstree 171, 45147 Essen, Germany

4. Forschungszentrum für Elektronenmikroskopie und Gerätezentrum BioSupraMol, Institut für Chemie und Biochemie, Freie Universität Berlin, Berlin 14195, Germany

5. Institut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany

6. Max-Planck Institute for the Physics of Complex Systems, Nöthnitzer Street 38, Dresden 01187, Germany

7. Institut für Physik, Universität Augsburg, Augsburg 86159, Germany

Funder

Deutsche Forschungsgemeinschaft

Berlin University Alliance

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.2c00166

Reference34 articles.

1. A brief review of influenza virus infection

2. Multivalent Peptide-Nanoparticle Conjugates for Influenza-Virus Inhibition

3. Aptamers for Anti-Viral Therapeutics and Diagnostics

4. Linear polysialoside outperforms dendritic analogs for inhibition of influenza virus infection in vitro and in vivo

5. Chemoenzymatic synthesis and application of a sialoglycopolymer with a chitosan backbone as a potent inhibitor of human influenza virus hemagglutination

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