tetano
Editor, Senior Moderator
PLoS One. 2013;8(1):e54070. doi: 10.1371/journal.pone.0054070. Epub 2013 Jan 10.
An assay suitable for high throughput screening of anti-influenza drugs.
Mao L, Wang J, Degrado WF, Inouye M.
Source
Department of Biochemistry and Center for Advanced Biotechnology and Medicine, Robert Wood Johnson Medical School, Piscataway, New Jersey, United States of America.
Abstract
We developed a novel drug screening system for anti-influenza A virus by targeting the M2 proton channel. In the SPP (Single Protein Production) system, E. coli cell growth occurs only in the presence of effective M2 channel inhibitors, and thus simple measurement of cell growth was used as readouts for drug screening. Two potential inhibitors for M2 (V27A) mutant were verified using this method, which inhibit both the mutant and wild-type M2 channels.
PMID:
23326573
[PubMed - in process]
PMCID:
PMC3542334
Free PMC Article
http://www.ncbi.nlm.nih.gov/pubmed/23326573
An assay suitable for high throughput screening of anti-influenza drugs.
Mao L, Wang J, Degrado WF, Inouye M.
Source
Department of Biochemistry and Center for Advanced Biotechnology and Medicine, Robert Wood Johnson Medical School, Piscataway, New Jersey, United States of America.
Abstract
We developed a novel drug screening system for anti-influenza A virus by targeting the M2 proton channel. In the SPP (Single Protein Production) system, E. coli cell growth occurs only in the presence of effective M2 channel inhibitors, and thus simple measurement of cell growth was used as readouts for drug screening. Two potential inhibitors for M2 (V27A) mutant were verified using this method, which inhibit both the mutant and wild-type M2 channels.
PMID:
23326573
[PubMed - in process]
PMCID:
PMC3542334
Free PMC Article
http://www.ncbi.nlm.nih.gov/pubmed/23326573