@article {2012|1960,
	title = {General Anesthetics Predicted to Block the {GLIC} Pore with Micromolar Affinity},
	journal = {Plos Comput. Biol.},
	volume = {8},
	number = {5},
	year = {2012},
	pages = {e1002532},
	publisher = {Public Library of Science},
	abstract = {<p>Author Summary</p> <p>Although general anesthesia is performed every day on thousands of people, its detailed microscopic mechanisms are not known. What is known is that general anesthetic drugs modulate the activity of ion channels in the central nervous system. These channels are proteins that open in response to binding of neurotransmitter molecules, creating an electric current through the cell membrane and thus propagating nerve impulses between cells. One possible mechanism for ion channel inhibition by anesthetics is that the drugs bind inside the pore of the channels, blocking ion current. Here we investigate such a pore block mechanism by computing the strength of the drugs{\textquoteright} interaction with the pore {\textendash} and hence the likelihood of binding, in the case of GLIC, a bacterial channel protein. The results, obtained from numerical simulations of atomic models of GLIC, indicate that the anesthetics isoflurane and propofol have a tendency to bind in the pore that is strong enough to explain blocking of the channel, even at low concentration of the drugs.</p>},
	doi = {10.1371/journal.pcbi.1002532},
	url = {http://dx.doi.org/10.1371\%2Fjournal.pcbi.1002532},
	author = {LeBard, David N. and J{\'e}r{\^o}me H{\'e}nin and Roderic G Eckenhoff and Michael L Klein and Brannigan, Grace}
}
