DocumentCode
1449820
Title
Modeling Study of the Light Stimulation of a Neuron Cell With Channelrhodopsin-2 Mutants
Author
Grossman, Nir ; Nikolic, Konstantin ; Toumazou, Christofer ; Degenaar, Patrick
Author_Institution
Inst. of Biomed. Eng., Imperial Coll. London, Imperial, CA, USA
Volume
58
Issue
6
fYear
2011
fDate
6/1/2011 12:00:00 AM
Firstpage
1742
Lastpage
1751
Abstract
Channelrhodopsin-2 (ChR2) has become a widely used tool for stimulating neurons with light. Nevertheless, the underlying dynamics of the ChR2-evoked spikes are still not yet fully understood. Here, we develop a model that describes the response of ChR2-expressing neurons to light stimuli and use the model to explore the light-to-spike process. We show that an optimal stimulation yield is achieved when the optical energies are delivered in short pulses. The model allows us to theoretically examine the effects of using various types of ChR2 mutants. We show that while increasing the lifetime and shuttering speed of ChR2 have limited effect, reducing the threshold irradiance by increased conductance will eliminate adaptation and allow constant dynamic range. The model and the conclusion presented in this study can help to interpret experimental results, design illumination protocols, and seek improvement strategies in the nascent optogenetic field.
Keywords
bioelectric phenomena; cellular biophysics; neurophysiology; photosynthesis; physiological models; proteins; channelrhodopsin-2 mutants; design illumination protocols; light stimulation; light-to-spike process; nascent optogenetic field; optical energies; optimal stimulation yield; photosynthesis; seek improvement strategies; shuttering speed; threshold irradiance; Adaptation model; Biomembranes; Electric potential; Lighting; Neurons; Photoconductivity; Biophysics; channelrhodopsin (ChR2); modeling; neurostimulation; optogenetics; Animals; CA3 Region, Hippocampal; Chlamydomonas reinhardtii; Evoked Potentials; Ion Channels; Light; Models, Neurological; Mutation; Neural Conduction; Neurons; Plant Proteins; Rats; Rhodopsin;
fLanguage
English
Journal_Title
Biomedical Engineering, IEEE Transactions on
Publisher
ieee
ISSN
0018-9294
Type
jour
DOI
10.1109/TBME.2011.2114883
Filename
5713238
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