TY - JOUR
T1 - Neuronal PDZ domains
T2 - A promising new molecular target for inhaled anesthetics?
AU - Tao, Yuan Xiang
AU - Johns, Roger A.
PY - 2004/8
Y1 - 2004/8
N2 - Despite widespread use of volatile general anesthetics in millions of patients each year, the mechanisms by which they exert multiple effects on the behavior of central neurons are poorly understood. PDZ [postsynaptic density 95 (PSD-95), discs large (Dlg), and zonula occludens-1 (Z0-1)] domains are ubiquitous protein interaction modules that participate in neuronal signaling. Recent studies have indicated that clinically relevant concentrations of inhaled anesthetics dose-dependently and specifically inhibit the PDZ domain-mediated protein interactions among multiprotein signaling complexes. These inhibitory effects are immediate, potent, reversible, and occur at a hydrophobic peptide-binding groove on the surface of the PDZ domain. Thus, the PDZ domain might be a new molecular target for inhalational anesthetics.
AB - Despite widespread use of volatile general anesthetics in millions of patients each year, the mechanisms by which they exert multiple effects on the behavior of central neurons are poorly understood. PDZ [postsynaptic density 95 (PSD-95), discs large (Dlg), and zonula occludens-1 (Z0-1)] domains are ubiquitous protein interaction modules that participate in neuronal signaling. Recent studies have indicated that clinically relevant concentrations of inhaled anesthetics dose-dependently and specifically inhibit the PDZ domain-mediated protein interactions among multiprotein signaling complexes. These inhibitory effects are immediate, potent, reversible, and occur at a hydrophobic peptide-binding groove on the surface of the PDZ domain. Thus, the PDZ domain might be a new molecular target for inhalational anesthetics.
UR - http://www.scopus.com/inward/record.url?scp=4444370650&partnerID=8YFLogxK
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U2 - https://doi.org/10.1124/mi.4.4.5
DO - https://doi.org/10.1124/mi.4.4.5
M3 - Review article
C2 - 15304557
SN - 1534-0384
VL - 4
SP - 215
EP - 221
JO - Molecular interventions
JF - Molecular interventions
IS - 4
ER -