Insight into the Mechanism of the Influenza A Proton Channel from a Structure in a Lipid Bilayer

Author:

Sharma Mukesh12,Yi Myunggi34,Dong Hao34,Qin Huajun1,Peterson Emily5,Busath David D.5,Zhou Huan-Xiang34,Cross Timothy A.124

Affiliation:

1. Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306, USA.

2. National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310, USA.

3. Department of Physics, Florida State University, Tallahassee, FL 32306, USA.

4. Institute of Molecular Biophysics, Florida State University, Tallahassee, FL 32306, USA.

5. Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84602, USA.

Abstract

M2 Out of the Envelope The M2 protein from influenza A virus forms an acid-activated tetrameric proton channel in the viral envelope and is essential for viral replication. Two manuscripts shed light on the functional mechanism of this channel. Sharma et al. (p. 509 ; see the Perspective by Fiorin et al. ) determined the structure of the conductance domain in a lipid bilayer and propose that a histidine and tryptophan from each monomer form a cluster that guides protons through the channel in a mechanism that involves forming and breaking hydrogen bonds between adjacent pairs of histidines. Hu et al. (p. 505 ; see the Perspective by Fiorin et al. ) focused on the structure and dynamics of the proton-selective histidine at high and low pH, proposing that proton conduction involves histidine deprotonation and reprotonation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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