TY - JOUR
T1 - Fast Kinetic Studies on the Allosteric Interactions between Acetylcholine Receptor and Local Anesthetic Binding Sites
AU - HEIDMANN, Thierry
AU - CHANGEUX, Jean‐Pierre ‐P
PY - 1979/1/1
Y1 - 1979/1/1
N2 - Preincubation of receptor‐rich membrane fragments from Torpedo marmorata with tertiary amine local anesthetics and several toxins such as histrionicotoxin, crotoxin and cerulotoxin, modifies the amplitude and time course of the relaxation processes monitored upon rapid mixing of the membrane fragments with the fluorescent agonist, Dns‐C6‐Cho. In particular, the amplitude of the rapid relaxation process, which is proportional to the fraction of acetylcholine receptor sites in a high‐affinity state, increases; accordingly, the rate constant of the ‘slow’ and ‘intermediate’ relaxation processes also increases up to ten times (except with histrionicotoxin) whereas in a higher range of local anesthetic concentrations the rate constant of the ‘rapid’ relaxation processes decreases. The data are accounted for by a two‐state model of the acetylcholine regulator, assuming distinct binding sites for cholinergic agonists and local anesthetics and allosteric interactions between these two classes of sites; local anesthetics stabilize the regulator in a high‐affinity state for agonists even in the absence of agonist, and modify the rate constants for the interconversions between the low‐affinity and high‐affinity states. The model accounts for the ‘slow’ fluorescence increase monitored upon addition of local anesthetics to a suspension of receptor‐rich membranes supplemented with trace amounts of Dns‐C6‐Cho. The effect of local anesthetics on the apparent rate constant of the ‘rapid’ relaxation process can be accounted for on the basis of an additional low‐affinity binding of local anesthetics to the acetylcholine receptor site. Finally the increase of the apparent rate constant of the ‘intermediate’ relaxation process can be simply accounted for by assuming the existence of a third state, corresponding to the ‘active’ state, to which local anesthetics bind and block ionic transport.
AB - Preincubation of receptor‐rich membrane fragments from Torpedo marmorata with tertiary amine local anesthetics and several toxins such as histrionicotoxin, crotoxin and cerulotoxin, modifies the amplitude and time course of the relaxation processes monitored upon rapid mixing of the membrane fragments with the fluorescent agonist, Dns‐C6‐Cho. In particular, the amplitude of the rapid relaxation process, which is proportional to the fraction of acetylcholine receptor sites in a high‐affinity state, increases; accordingly, the rate constant of the ‘slow’ and ‘intermediate’ relaxation processes also increases up to ten times (except with histrionicotoxin) whereas in a higher range of local anesthetic concentrations the rate constant of the ‘rapid’ relaxation processes decreases. The data are accounted for by a two‐state model of the acetylcholine regulator, assuming distinct binding sites for cholinergic agonists and local anesthetics and allosteric interactions between these two classes of sites; local anesthetics stabilize the regulator in a high‐affinity state for agonists even in the absence of agonist, and modify the rate constants for the interconversions between the low‐affinity and high‐affinity states. The model accounts for the ‘slow’ fluorescence increase monitored upon addition of local anesthetics to a suspension of receptor‐rich membranes supplemented with trace amounts of Dns‐C6‐Cho. The effect of local anesthetics on the apparent rate constant of the ‘rapid’ relaxation process can be accounted for on the basis of an additional low‐affinity binding of local anesthetics to the acetylcholine receptor site. Finally the increase of the apparent rate constant of the ‘intermediate’ relaxation process can be simply accounted for by assuming the existence of a third state, corresponding to the ‘active’ state, to which local anesthetics bind and block ionic transport.
UR - http://www.scopus.com/inward/record.url?scp=0018762233&partnerID=8YFLogxK
U2 - 10.1111/j.1432-1033.1979.tb12894.x
DO - 10.1111/j.1432-1033.1979.tb12894.x
M3 - Article
C2 - 436844
AN - SCOPUS:0018762233
SN - 0014-2956
VL - 94
SP - 281
EP - 296
JO - European Journal of Biochemistry
JF - European Journal of Biochemistry
IS - 1
ER -