1. Department of Molecular and Integrative Physiology, Center for Biophysics and Computational Biology, and Neuroscience Program, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA

Correspondence to: Claudio Grosman¹ Correspondence and requests for materials should be addressed to C.G. (Email: grosman@life.uiuc.edu).

Abstract

Although membrane proteins often rely on ionizable residues for structure and function, their ionization states under physiological conditions largely elude experimental estimation. To gain insight into the effect of the local microenvironment on the proton affinity of ionizable residues, we have engineered individual lysines, histidines and arginines along the -helical lining of the transmembrane pore of the nicotinic acetylcholine receptor. We can detect individual proton binding–unbinding reactions electrophysiologically at the level of a single proton on a single side chain as brief blocking–unblocking events of the passing cation current. Kinetic analysis of these fluctuations yields the position-dependent rates of proton transfer, from which the corresponding pK_a values and shifts in pK_a can be calculated. Here we present a self-consistent, residue-by-residue description of the microenvironment around the pore-lining transmembrane -helices (M2) in the open-channel conformation, in terms of the excess free energy that is required to keep the engineered basic side chains protonated relative to bulk water. A comparison with closed-channel data leads us to propose that the rotation of M2, which is frequently invoked as a hallmark of the gating mechanism of Cys-loop receptors, is minimal, if any.

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