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How light triggers brain activity

Protein research

Date:
April 23, 2019
Source:
Ruhr-University Bochum
Summary:
Optogenetics uses light to control brain processes. It is based on light-controlled proteins such as channelrhodopsin-2, an ion channel that opens when it's exposed to light, thus activating cellular processes. The researchers have now shed light on its mode of action.
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Optogenetics uses light to control brain processes. It is based on light-controlled proteins such as channelrhodopsin-2, an ion channel that opens when it's exposed to light, thus activating cellular processes. The researchers have now shed light on its mode of action.

Enormous therapeutic potential

Researchers consider optogenetics to have enormous therapeutic potential. "It is feasible that light might be used to make blind people see or to treat agitated paralysis in Parkinson's patients," explains Klaus Gerwert.

Discovered by Peter Hegemann, channelrhodopsin-2 is the central light-activated protein in optogenetics. If this ion channel is applied to nerve cells, the channels can be opened by light, thus activating the cell.

In the past scientists could not agree on how the channel is activated. "But it is precisely the understanding of the molecular reactions in the protein and of the ionic conductivity resulting thereof that is essential for optimising the protein for its potential applications," says Gerwert.

Two parallel paths

With joined forces, the researchers from Bochum and Berlin figured out how the channel is activated in detail. By combining time-resolved Fourier Transform Infrared Spectroscopy, biomolecular simulations, and electrophysiological experiments, they demonstrated that photoexcitation triggers two different structures -- and not, as previously assumed, only one. One of them results in the required channel activation that is used in optogenetics. The parallel path provides merely a weak proton stream; however, the longer exposure, the more it gains the upper hand and suppresses the required channel activation. Accordingly, the optogenetic tool soon starts to lose its effectiveness. "If we block the unwanted parallel path by implementing specific protein design, we could optimise the optogenetic tool considerably," concludes Gerwert.

Conducting research into channelrhodopsin, the Bochum-based researchers drew on their extensive experience regarding the mechanism of the light-driven proton pump bacteriorhodopsin, which they solved in detail several years ago. "Just as in bacteriorhodopsin, protein-bound water molecules play a crucial role in proton conductivity," explains Klaus Gerwert.


Story Source:

Materials provided by Ruhr-University Bochum. Note: Content may be edited for style and length.


Journal Reference:

  1. Jens Kuhne, Johannes Vierock, Stefan Alexander Tennigkeit, Max-Aylmer Dreier, Jonas Wietek, Dennis Petersen, Konstantin Gavriljuk, Samir F. El-Mashtoly, Peter Hegemann, Klaus Gerwert. Unifying photocycle model for light adaptation and temporal evolution of cation conductance in channelrhodopsin-2. Proceedings of the National Academy of Sciences, 2019; 201818707 DOI: 10.1073/pnas.1818707116

Cite This Page:

Ruhr-University Bochum. "How light triggers brain activity." ScienceDaily. ScienceDaily, 23 April 2019. <www.sciencedaily.com/releases/2019/04/190423133620.htm>.
Ruhr-University Bochum. (2019, April 23). How light triggers brain activity. ScienceDaily. Retrieved December 10, 2024 from www.sciencedaily.com/releases/2019/04/190423133620.htm
Ruhr-University Bochum. "How light triggers brain activity." ScienceDaily. www.sciencedaily.com/releases/2019/04/190423133620.htm (accessed December 10, 2024).

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