Literature DB >> 32817125

Finding proteases that make cells go viral.

Hector C Aguilar1, David W Buchholz2.   

Abstract

The activation of influenza virus hemagglutinin (HA) glycoprotein via cleavage by host cell proteases is essential for viral infectivity, and understanding the mechanisms for HA protein cleavage and how they may differ depending on the biological context is important for the development of flu treatments. However, the HA proteases involved in the activation of many viral strains remain unidentified. In this issue, Harbig et al. identify a repertoire of proteases that cleave HA and determine the proteases' functionality against specific HA glycoproteins.
© 2020 Aguilar and Buchholz.

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Year:  2020        PMID: 32817125      PMCID: PMC7450131          DOI: 10.1074/jbc.H120.015153

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  8 in total

1.  Proteolytic activation of influenza viruses by serine proteases TMPRSS2 and HAT from human airway epithelium.

Authors:  Eva Böttcher; Tatyana Matrosovich; Michaela Beyerle; Hans-Dieter Klenk; Wolfgang Garten; Mikhail Matrosovich
Journal:  J Virol       Date:  2006-10       Impact factor: 5.103

Review 2.  Aprotinin and similar protease inhibitors as drugs against influenza.

Authors:  O P Zhirnov; H D Klenk; P F Wright
Journal:  Antiviral Res       Date:  2011-07-23       Impact factor: 5.970

Review 3.  Role of hemagglutinin cleavage for the pathogenicity of influenza virus.

Authors:  D A Steinhauer
Journal:  Virology       Date:  1999-05-25       Impact factor: 3.616

4.  Transcriptome profiling and protease inhibition experiments identify proteases that activate H3N2 influenza A and influenza B viruses in murine airways.

Authors:  Anne Harbig; Marco Mernberger; Linda Bittel; Stephan Pleschka; Klaus Schughart; Torsten Steinmetzer; Thorsten Stiewe; Andrea Nist; Eva Böttcher-Friebertshäuser
Journal:  J Biol Chem       Date:  2020-04-17       Impact factor: 5.157

5.  TMPRSS2 is a host factor that is essential for pneumotropism and pathogenicity of H7N9 influenza A virus in mice.

Authors:  Carolin Tarnow; Géraldine Engels; Annika Arendt; Folker Schwalm; Hanna Sediri; Annette Preuss; Peter S Nelson; Wolfgang Garten; Hans-Dieter Klenk; Gülsah Gabriel; Eva Böttcher-Friebertshäuser
Journal:  J Virol       Date:  2014-02-12       Impact factor: 5.103

6.  SARS-CoV-2 entry factors are highly expressed in nasal epithelial cells together with innate immune genes.

Authors:  Waradon Sungnak; Ni Huang; Christophe Bécavin; Marijn Berg; Rachel Queen; Monika Litvinukova; Carlos Talavera-López; Henrike Maatz; Daniel Reichart; Fotios Sampaziotis; Kaylee B Worlock; Masahiro Yoshida; Josephine L Barnes
Journal:  Nat Med       Date:  2020-04-23       Impact factor: 53.440

7.  Tmprss2 is essential for influenza H1N1 virus pathogenesis in mice.

Authors:  Bastian Hatesuer; Stephanie Bertram; Nora Mehnert; Mahmoud M Bahgat; Peter S Nelson; Stefan Pöhlmann; Stefan Pöhlman; Klaus Schughart
Journal:  PLoS Pathog       Date:  2013-12-05       Impact factor: 6.823

8.  The Proteolytic Activation of (H3N2) Influenza A Virus Hemagglutinin Is Facilitated by Different Type II Transmembrane Serine Proteases.

Authors:  Nora Kühn; Silke Bergmann; Nadine Kösterke; Ruth L O Lambertz; Anna Keppner; Judith M A van den Brand; Stefan Pöhlmann; Siegfried Weiß; Edith Hummler; Bastian Hatesuer; Klaus Schughart
Journal:  J Virol       Date:  2016-04-14       Impact factor: 5.103

  8 in total

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