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Photoaffinity labeling of acetylcholine receptor in millisecond time scale
Photoaffinity labeling of acetylcholine receptors can be performed with a time resolution allowing to discriminate reaction sites within the receptor protein in its different functional states. This is achieved by a combination of a stopped-flow apparatus with a high energy pulse laser. The photoaff...
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Published in: | FEBS letters 1984-01, Vol.166 (1), p.146-150 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Photoaffinity labeling of acetylcholine receptors can be performed with a time resolution allowing to discriminate reaction sites within the receptor protein in its different functional states. This is achieved by a combination of a stopped-flow apparatus with a high energy pulse laser. The photoaffinity label used is the lipophilic cation [
3H]TPMP
+ which has been shown to be a non-competitive antagonist and a specific ion channel blocker. AChR in its resting (channel closed) and active (channel open) state incorporates the label mainly into the α-polypeptide chain of the receptor. Only several hundred milliseconds after mixing AChR with agonist labeling of δ-chains becomes significant. |
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ISSN: | 0014-5793 1873-3468 |
DOI: | 10.1016/0014-5793(84)80061-7 |