Literature DB >> 30230312

A Robust Proton Flux (pHlux) Assay for Studying the Function and Inhibition of the Influenza A M2 Proton Channel.

Paul Santner1, João Miguel da Silva Martins1, Jonas S Laursen2, Lars Behrendt1, Leise Riber3, Christian A Olsen2,4, Isaiah T Arkin5, Jakob R Winther1, Martin Willemoës1, Kresten Lindorff-Larsen1.   

Abstract

The M2 protein is an important target for drugs in the fight against the influenza virus. Because of the emergence of resistance against antivirals directed toward the M2 proton channel, the search for new drugs against resistant M2 variants is of high importance. Robust and sensitive assays for testing potential drug compounds on different M2 variants are valuable tools in this search for new inhibitors. In this work, we describe a fluorescence sensor-based assay, which we termed "pHlux", that measures proton conduction through M2 when synthesized from an expression vector in Escherichia coli. The assay was compared to a previously established bacterial potassium ion transport complementation assay, and the results were compared to simulations obtained from analysis of a computational model of M2 and its interaction with inhibitor molecules. The inhibition of M2 was measured for five different inhibitors, including Rimantadine, Amantadine, and spiro type compounds, and the drug resistance of the M2 mutant variants (swine flu, V27A, and S31N) was confirmed. We demonstrate that the pHlux assay is robust and highly sensitive and shows potential for high-throughput screening.

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Year:  2018        PMID: 30230312     DOI: 10.1021/acs.biochem.8b00721

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  8 in total

1.  The L46P mutant confers a novel allosteric mechanism of resistance toward the influenza A virus M2 S31N proton channel blockers.

Authors:  Rami Musharrafieh; Panagiotis I Lagarias; Chunlong Ma; Gene S Tan; Antonios Kolocouris; Jun Wang
Journal:  Mol Pharmacol       Date:  2019-06-07       Impact factor: 4.436

2.  SARS-CoV-2 E protein is a potential ion channel that can be inhibited by Gliclazide and Memantine.

Authors:  Prabhat Pratap Singh Tomar; Isaiah T Arkin
Journal:  Biochem Biophys Res Commun       Date:  2020-06-20       Impact factor: 3.575

3.  Potential Viroporin Candidates From Pathogenic Viruses Using Bacteria-Based Bioassays.

Authors:  Prabhat Pratap Singh Tomar; Rivka Oren; Miriam Krugliak; Isaiah T Arkin
Journal:  Viruses       Date:  2019-07-09       Impact factor: 5.048

4.  Searching for Blockers of Dengue and West Nile Virus Viroporins.

Authors:  Hiya Lahiri; Isaiah T Arkin
Journal:  Viruses       Date:  2022-08-11       Impact factor: 5.818

Review 5.  Put a cork in it: Plugging the M2 viral ion channel to sink influenza.

Authors:  Pouria H Jalily; Maggie C Duncan; David Fedida; Jun Wang; Ian Tietjen
Journal:  Antiviral Res       Date:  2020-03-27       Impact factor: 5.970

6.  Blockers of the SARS-CoV-2 3a Channel Identified by Targeted Drug Repurposing.

Authors:  Prabhat Pratap Singh Tomar; Miriam Krugliak; Isaiah T Arkin
Journal:  Viruses       Date:  2021-03-23       Impact factor: 5.048

7.  Identification of SARS-CoV-2 E Channel Blockers from a Repurposed Drug Library.

Authors:  Prabhat Pratap Singh Tomar; Miriam Krugliak; Isaiah T Arkin
Journal:  Pharmaceuticals (Basel)       Date:  2021-06-23

8.  Zika M-A Potential Viroporin: Mutational Study and Drug Repurposing.

Authors:  Prabhat Pratap Singh Tomar; Miriam Krugliak; Anamika Singh; Isaiah T Arkin
Journal:  Biomedicines       Date:  2022-03-10
  8 in total

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