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PMID: 6095896 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification of an opioid receptor subunit carrying the mu binding site.

Biochemistry ·Vol. 23 ·No. 23 ·1984-11-06 ·Pages 5385-9

Newman EL, Barnard EA

Abstract

The enkephalin affinity reagent [3H]Tyr-D-Ala-Gly-Phe-Leu-CH2Cl [( 3H]DALECK) was synthesized. It exhibited high-affinity reversible binding, at pH 7.4, to both mu and delta opioid receptor sites in rat brain membranes. At pH 8.1, nanomolar levels of [3H]DALECK produced an irreversible labeling in synaptic membranes, essentially only in one subunit of 58 000 daltons. The irreversible phase of the reaction reduced the subsequent binding of a mu-selective enkephalin derivative but not that of a delta-selective one. It is concluded that a mu subunit of the opioid receptor exists, can be alkylated specifically, and is of Mr 58 000.

MeSH Terms
Affinity Labels/metabolism Alkylation Amino Acid Chloromethyl Ketones/chemical synthesis,metabolism Animals Binding Sites Brain/metabolism Enkephalin, Ala(2)-MePhe(4)-Gly(5)- Enkephalin, Leucine/analogs & derivatives,metabolism Enkephalin, Leucine-2-Alanine Enkephalins/metabolism Hydrogen-Ion Concentration Intracellular Membranes/metabolism Microsomes/metabolism Mitochondria/metabolism Molecular Weight Rats Receptors, Opioid/metabolism Synaptic Membranes/metabolism
Chemicals
Affinity Labels Amino Acid Chloromethyl Ketones Enkephalins Receptors, Opioid Enkephalin, Ala(2)-MePhe(4)-Gly(5)- Enkephalin, Leucine Enkephalin, Leucine-2-Alanine tyrosyl-alanyl-glycyl-phenylalanyl-leucine chloromethyl ketone
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Newman E L
Barnard E A
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1984-11-06
Pages
5385-9
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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