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Proc Natl Acad Sci U S A. 2017 Dec 19;114(51):13357-13362. doi: 10.1073/pnas.1705624114. Epub 2017 Aug 23.

XFEL structures of the influenza M2 proton channel: Room temperature water networks and insights into proton conduction.

Author information

1
Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158.
2
Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158.
3
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.
4
SPring-8 Angstrom Compact Free Electron Laser (SACLA) Science Research Group, RIKEN SPring-8 Center, Saitama 351-0198, Japan.
5
Structural Biology Research Center, High Energy Accelerator Research Organization (KEK), Ibaraki 305-0801, Japan.
6
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720.
7
School of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853.
8
Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305.
9
Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305.
10
Department of Neurology and Neurological Sciences, Stanford University, Palo Alto, CA 94304.
11
Department of Photon Science, Stanford University, Stanford, CA 94305.
12
Department of Structural Biology, Stanford University, Stanford, CA 94305.
13
Division of Food Science and Biotechnology, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.
14
Institute for Protein Research, Osaka University, Osaka 565-0871, Japan.
15
Experimental Instrumentation Team, Japan Synchrotron Radiation Research Institute, Hyogo 679-5198, Japan.
16
Department of Cell Biology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.
17
Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158; william.degrado@ucsf.edu.

Abstract

The M2 proton channel of influenza A is a drug target that is essential for the reproduction of the flu virus. It is also a model system for the study of selective, unidirectional proton transport across a membrane. Ordered water molecules arranged in "wires" inside the channel pore have been proposed to play a role in both the conduction of protons to the four gating His37 residues and the stabilization of multiple positive charges within the channel. To visualize the solvent in the pore of the channel at room temperature while minimizing the effects of radiation damage, data were collected to a resolution of 1.4 Å using an X-ray free-electron laser (XFEL) at three different pH conditions: pH 5.5, pH 6.5, and pH 8.0. Data were collected on the Inwardopen state, which is an intermediate that accumulates at high protonation of the His37 tetrad. At pH 5.5, a continuous hydrogen-bonded network of water molecules spans the vertical length of the channel, consistent with a Grotthuss mechanism model for proton transport to the His37 tetrad. This ordered solvent at pH 5.5 could act to stabilize the positive charges that build up on the gating His37 tetrad during the proton conduction cycle. The number of ordered pore waters decreases at pH 6.5 and 8.0, where the Inwardopen state is less stable. These studies provide a graphical view of the response of water to a change in charge within a restricted channel environment.

KEYWORDS:

XFEL; influenza; membrane protein; proton channel

PMID:
28835537
PMCID:
PMC5754760
DOI:
10.1073/pnas.1705624114
[Indexed for MEDLINE]
Free PMC Article

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