Can you elaborate on the damage that is occurring, even with cryoprotectants?
Why/how would low temps in a cryoprotectant denature proteins?
If you have time I would really like to see the detailed posts, perhaps even in a new thread. I am also a bioengineer/biophysicist but I have little knowledge of neuroscience.
I'll eventually organize my thoughts in something worthy of a post. Until then, this has already gone into way more detail than I intended. Thus, briefly:
The damage that is occurring - distortion of membranes, denaturation of proteins (very likely), disruption of signalling pathways. Just changing the exact localization of Ca microdomains within a synapse can wreak havoc, replacing the liquid completely? Not going to work.
I don't necessarily think that low temps have anything to do with denaturation. Replacing the solvent, however, would do it almost unav...
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