The techniques I've heard of are:

1. Switch to glass electrodes (not compatible with my experiments)

2. Play around with relative positions of fiber optic and electrode (all locations I've tried still end up with artifact -- but we are very constrained in space so not much flexibility)

3. Record the light artifact alone elsewhere in the brain and subtract it out before doing spike sorting. 

Is #3 really reliable? Any issues to be aware of? Any other ideas/other metals/coatings that might help?

Details: I'm delivering short pulses of light (473 nm, 2 ms) in awake, head-fixed mice and recording the response in ChR2-expressing neurons. Currently using tungsten wires (1.5 MOhm) coated with parylene-c. Light is generated by a laser and delivered via a fiber optic, inserted through the same guide tube as the electrode, and positioned 0-2 mm back from the tip of the electrode. 

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