Source:http://linkedlifedata.com/resource/pubmed/id/19946785
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-2-24
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pubmed:abstractText |
Influenza A virus encodes an integral membrane protein, A/M2, that forms a pH-gated proton channel that is essential for viral replication. The A/M2 channel is a target for the anti-influenza drug amantadine, although the effectiveness of this drug has been diminished by the appearance of naturally occurring point mutations in the channel pore. Thus, there is a great need to discover novel anti-influenza therapeutics, and, since the A/M2 channel is a proven target, approaches are needed to screen for new classes of inhibitors for the A/M2 channel. Prior in-depth studies of the activity and drug sensitivity of A/M2 channels have employed labor-intensive electrophysiology techniques. In this study, we tested the validity of electrophysiological measurements with solid-supported membranes (SSM) as a less labor-intensive alternative technique for the investigation of A/M2 ion channel properties and for drug screening. By comparing the SSM-based measurements of the activity and drug sensitivity of A/M2 wild-type and mutant channels with measurements made with conventional electrophysiology methods, we show that SSM-based electrophysiology is an efficient and reliable tool for functional studies of the A/M2 channel protein and for screening compounds for inhibitory activity against the channel.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/GM56416,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI-57363,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI-74517,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI057363-05,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI071342-01,
http://linkedlifedata.com/resource/pubmed/grant/U01 AI1074571
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1432-2013
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
459
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
593-605
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pubmed:dateRevised |
2011-9-22
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pubmed:meshHeading |
pubmed-meshheading:19946785-Amantadine,
pubmed-meshheading:19946785-Animals,
pubmed-meshheading:19946785-Antiviral Agents,
pubmed-meshheading:19946785-CHO Cells,
pubmed-meshheading:19946785-Cell Membrane,
pubmed-meshheading:19946785-Cricetinae,
pubmed-meshheading:19946785-Cricetulus,
pubmed-meshheading:19946785-Drug Resistance, Viral,
pubmed-meshheading:19946785-Electrophysiology,
pubmed-meshheading:19946785-Humans,
pubmed-meshheading:19946785-Influenza A virus,
pubmed-meshheading:19946785-Microbial Sensitivity Tests,
pubmed-meshheading:19946785-Reproducibility of Results,
pubmed-meshheading:19946785-Viral Matrix Proteins,
pubmed-meshheading:19946785-Virus Replication
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pubmed:year |
2010
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pubmed:articleTitle |
Solid-supported membrane technology for the investigation of the influenza A virus M2 channel activity.
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pubmed:affiliation |
Department of Neurobiology and Physiology, Northwestern University, Hogan Hall, 2205 Tech Drive, Evanston, IL 60208-3500, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Evaluation Studies,
Research Support, N.I.H., Extramural
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