Delimiting the binding site for quaternary ammonium lidocaine derivatives in the acetylcholine receptor channel

Juan M. Pascual, Arthur Karlin

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

The triethylammonium QX-314 and the trimethylammonium QX-222 are lidocaine derivatives that act as open-channel blockers of the acetylcholine (ACh) receptor. When bound, these blockers should occlude some of the residues lining the channel. Eight residues in the second membrane-spanning segment (M2) of the mouse-muscle α subunit were mutated one at a time to cysteine and expressed together with wild-type β, γ, and δ subunits in Xenopus oocytes. The rate constant for the reaction of each substituted cysteine with 2-aminoethyl methanethiosulfonate (MTSEA) was determined from the time course of the irreversible effect of MTSEA on the ACh-induced current. The reactions were carried out in the presence and absence of ACh and in the presence and absence of QX-314 and QX-222. These blockers had no effect on the reactions in the absence of ACh. In the presence of ACh, both blockers retarded the reaction of extracellularly applied MTSEA with cysteine substituted for residues from αVal255, one third of the distance in from the extracellular end of M2, to αGlu241, flanking the intracellular end of M2, but not with cysteine substituted for αLeu258 or αGlu262, at the extracellular end of M2. The reactions of MTSEA with cysteines substituted for αLeu258 and αGlu262 were considerably faster in the presence of ACh than in its absence. That QX-314 and QX-222 did not protect αL258C and αE262C against reaction with MTSEA in the presence of ACh implies that protection of the other residues was due to occlusion of the channel and not to the promotion of a less reactive state from a remote site. Given the 12- Å overall length of the blockers and the α-helical conformation of M2 in the open state, the binding site for both blockers extends from αVal255 down to αSer248.

Original languageEnglish (US)
Pages (from-to)611-621
Number of pages11
JournalJournal of General Physiology
Volume112
Issue number5
DOIs
StatePublished - Nov 1998

Fingerprint

Cholinergic Receptors
Lidocaine
Ammonium Compounds
Acetylcholine
Binding Sites
Cysteine
Xenopus
Oocytes
methanethiosulfonate ethylammonium
Muscles
Membranes
QX-222
QX-314

Keywords

  • Cysteine mutagenesis
  • Methanethiosulfonate
  • Open- channel block
  • Reaction kinetics

ASJC Scopus subject areas

  • Physiology

Cite this

Delimiting the binding site for quaternary ammonium lidocaine derivatives in the acetylcholine receptor channel. / Pascual, Juan M.; Karlin, Arthur.

In: Journal of General Physiology, Vol. 112, No. 5, 11.1998, p. 611-621.

Research output: Contribution to journalArticle

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