Giuseppe
Emeritus
Biochem Biophys Res Commun. 2008 Nov 5. [Epub ahead of print]
An in-depth analysis of the biological functional studies based on the NMR M2 channel structure of influenza A virus.
Huang RB, Du QS, Wang CH, Chou KC. - Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530004, China.
The long-sought three-dimensional structure of the M2 proton channel of influenza A virus was successfully determined recently by the high-resolution NMR [J.R. Schnell, J.J. Chou, Structure and mechanism of the M2 proton channel of influenza A virus, Nature 451 (2008) 591-595].
Such a milestone work has provided a solid structural basis for studying drug-resistance problems.
However, the action mechanism revealed from the NMR structure is completely different from the traditional view and hence prone to be misinterpreted as "conflicting" with some previous biological functional studies.
To clarify this kind of confusion, an in-depth analysis was performed for these functional studies, particularly for the mutations D44N, D44A and N44D on position 44, and the mutations on positions 27-38.
The analyzed results have provided not only compelling evidences to further validate the NMR structure but also very useful clues for dealing with the drug-resistance problems and developing new effective drugs against H5N1 avian influenza virus, an impending threat to human beings.
PMID: 18996090 [PubMed - as supplied by publisher
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An in-depth analysis of the biological functional studies based on the NMR M2 channel structure of influenza A virus.
Huang RB, Du QS, Wang CH, Chou KC. - Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530004, China.
The long-sought three-dimensional structure of the M2 proton channel of influenza A virus was successfully determined recently by the high-resolution NMR [J.R. Schnell, J.J. Chou, Structure and mechanism of the M2 proton channel of influenza A virus, Nature 451 (2008) 591-595].
Such a milestone work has provided a solid structural basis for studying drug-resistance problems.
However, the action mechanism revealed from the NMR structure is completely different from the traditional view and hence prone to be misinterpreted as "conflicting" with some previous biological functional studies.
To clarify this kind of confusion, an in-depth analysis was performed for these functional studies, particularly for the mutations D44N, D44A and N44D on position 44, and the mutations on positions 27-38.
The analyzed results have provided not only compelling evidences to further validate the NMR structure but also very useful clues for dealing with the drug-resistance problems and developing new effective drugs against H5N1 avian influenza virus, an impending threat to human beings.
PMID: 18996090 [PubMed - as supplied by publisher
-
-----