Abstract
The slow inward calcium channel, identified by physiologic and pharmacologic responses and [3H]nitrendipine-specific binding, has been characterized by radiation inactivation and covalent affinity labeling. Target size analysis of guinea pig ileum longitudinal smooth muscle membranes indicates a molecular weight of 278,000 for the calcium channel. An affinity label analog of nifedipine and nitrendipine, 2,6-dimethyl-3,5-dicarbomethoxy-4-(2-isothiocyanatophenyl)-1,4-dihydropyridine, was found to inhibit the calcium channel by a covalent interaction with a protein subunit (Mr = 45,000) of the calcium channel.
| Original language | English |
|---|---|
| Pages (from-to) | 9344-9348 |
| Number of pages | 5 |
| Journal | Journal of Biological Chemistry |
| Volume | 258 |
| Issue number | 15 |
| DOIs | |
| State | Published - Aug 10 1983 |
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