Location in Muscarinic Acetylcholine Receptors of Sites for [³H]Propylbenzilcholine Mustard Binding and for Phosphorylation with Protein Kinase C

<jats:p><jats:bold>Abstract: </jats:bold> Muscarinic acetylcholine receptors purified from porcine cerebra or atria were covalently labeled with [<jats:sup>3</jats:sup>H]propylbenzilylcholine mustard ([<jats:sup>3</jats:sup>H]PrBCM), and then the labeled receptors were subjected to limited hydrolysis with trypsin, V8 protease, and lysyl endopeptidase, followed by analysis involving sodium dodecyl sulfate‐polyacrylamide gel electrophoresis, fluorography, autoradiography, or immunostaining. The labeled peptides were located on the basis of their reactivity with antibodies raised against three synthetic peptides with partial sequences of the m1 or m2 receptor, and of their sensitivity to endoglycosidase F, which was taken as evidence that they contain glycosylation sites near the N terminus. The [<jats:sup>3</jats:sup>H]PrBCM‐binding site in both cerebral and atrial receptors was found to be located between the N terminus and the second intracellular loop, because the size of the smallest deglycosylated peptide that contained both the [<jats:sup>3</jats:sup>H]PrBCM‐binding and glycosylation sites was ∼ 16 kDa. Cerebral receptors were <jats:sup>32</jats:sup>P‐phosphorylated with protein kinase C, and the major phosphorylation sites in cerebral muscarinic receptors were found to be located in a C‐terminal segment including a part of the third intracellular loop, because a <jats:sup>32</jats:sup>P‐labeled peptide of 12–14 kDa reacted with anti‐(m 1 C‐terminal peptide) antiserum. The presence of an intramolecular disulfide bond, probably between Cys 98 and Cys 178 in the first and second extracellular loops, respectively, was suggested by the finding that a peptide of ∼ 17 kDa containing the [<jats:sup>3</jats:sup>H]PrBCM‐binding site, but not the glycosylation sites, was partly converted to a peptide of ∼ 12 kDa on treatment with β‐mercaptoethanol.</jats:p>