Litcius/Paper detail

Imidazole–Imidazole Hydrogen Bonding in the pH-Sensing Histidine Side Chains of Influenza A M2

Kumar Tekwani Movellan, Melanie Wegstroth, Kerstin Overkamp, Andrei Leonov, Stefan Becker, Loren B. Andreas

2020Journal of the American Chemical Society49 citationsDOIOpen Access PDF

Abstract

The arrangement of histidine side chains in influenza A M2 tetramer determines their pKa values, which define pH-controlled proton conduction critical to the virus lifecycle. Both water-associated and hydrogen-bonded imidazole–imidazolium histidine quaternary structures have been proposed, based on crystal structures and NMR chemical shifts, respectively. Here we show, using the conduction domain construct of M2 in lipid bilayers, that the imidazole rings are hydrogen bonded even at a pH of 7.8 in the neutral charge state. An intermolecular 8.9 ± 0.3 Hz 2hJNN hydrogen bond is observed between H37 Nε and Nδ recorded in a fully protonated sample with 100 kHz magic-angle spinning. This interaction could not be detected in the drug-bound sample.

Topics & Concepts

ChemistryImidazoleHydrogen bondSide chainProtonationTetramerCrystallographyHistidineIntermolecular forceStereochemistryMoleculeOrganic chemistryEnzymeIonPolymerInfluenza Virus Research StudiesLipid Membrane Structure and BehaviorAdvanced NMR Techniques and Applications