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Optogenetic tool elucidated: Opening of the ion channel with light

Date:
February 28, 2012
Source:
Ruhr-Universitaet-Bochum
Summary:
Controlling nerve cells with the aid of light: this is made possible by optogenetics. It enables, for example, the investigation of neurobiological processes with unprecedented spatial and temporal precision. Biophysicists have now succeeded in explaining the switching mechanism.

The Bochum homology model predicts the structure of a channelrhodopsin so well that it has been even possible to make statements about its function. The illustration shows the prediction in comparison to the later crystal structure.
Credit: Image courtesy of Ruhr-Universitaet-Bochum

Controlling nerve cells with the aid of light: this is made possible by optogenetics. It enables, for example, the investigation of neurobiological processes with unprecedented spatial and temporal precision. The key tool of optogenetics is the light-activated protein channelrhodopsin. Biophysicists from Bochum and Berlin have now succeeded in explaining the switching mechanism through an interdisciplinary approach. The researchers report on their findings in the Journal of Biological Chemistry.

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Redistribution of water molecules

Until now, little has been known about the mechanism of the protein -- especially about how the channel opens. However, deeper understanding is a prerequisite in order to be able to use the light-controlled protein specifically for neurobiological applications. In a new, multi-disciplinary approach, the Bochum scientists led by Prof. Dr. Klaus Gerwert (Department of Biophysics at the RUB) and their cooperation partners in Berlin have been able to shed light on the switching mechanism. The result: the light-induced change in the charge state of amino acid glutamate 90 (E90) triggers an increased penetration of water molecules, so that the protein can now purposefully conduct ions through the cell membrane.

Three methods combined

Using time-resolved infrared spectroscopy, the RUB biophysicists Jens Kuhne and Dr. Erik Freier have been able to show for the first time that the channel is opened through the deprotonation of the amino acid glutamate 90 (E90). In addition, the electrophysiological experiments of the researchers in Berlin confirm that a mutation of the amino acid leads to a change in the ion permeability of the protein. Instead of using safety goggles and lab coats, the two biophysicists Kirstin Eisenhauer and Dr. Steffen Wolf at the Department of Biophysics used supercomputers to simulate how the protonation change of the glutamate opens the channel and allows water molecules to penetrate.

Shortly after the Bochum pre-publication on the Internet, Japanese researchers published the three-dimensional structure of a channelrhodopsin online in Nature. "The structure work impressively confirms our biomolecular simulations and the key role played by the amino acid E90 in the switching of the channel," says Prof. Klaus Gerwert. "We are therefore particularly proud to have been preeminent in this internationally competitive field."


Story Source:

The above story is based on materials provided by Ruhr-Universitaet-Bochum. Note: Materials may be edited for content and length.


Journal Reference:

  1. K. Eisenhauer, J. Kuhne, E. Ritter, A. Berndt, S. Wolf, E. Freier, F. Bartl, P. Hegemann, K. Gerwert. In Channelrhodopsin-2 Glu-90 Is Crucial for Ion Selectivity and Is Deprotonated during the Photocycle. Journal of Biological Chemistry, 2012; 287 (9): 6904 DOI: 10.1074/jbc.M111.327700

Cite This Page:

Ruhr-Universitaet-Bochum. "Optogenetic tool elucidated: Opening of the ion channel with light." ScienceDaily. ScienceDaily, 28 February 2012. <www.sciencedaily.com/releases/2012/02/120228101710.htm>.
Ruhr-Universitaet-Bochum. (2012, February 28). Optogenetic tool elucidated: Opening of the ion channel with light. ScienceDaily. Retrieved October 25, 2014 from www.sciencedaily.com/releases/2012/02/120228101710.htm
Ruhr-Universitaet-Bochum. "Optogenetic tool elucidated: Opening of the ion channel with light." ScienceDaily. www.sciencedaily.com/releases/2012/02/120228101710.htm (accessed October 25, 2014).

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