Different Binding Orientations for the Same Agonist at Homologous Receptors: A Lock and Key or a Simple Wedge?
Abstract
Using unnatural amino acid mutagenesis, the binding site for serotonin at the novel Caenorhabditis elegans receptor MOD-1 has been probed. As with the closely related serotonin receptor 5-HT_3, MOD-1 makes use of a strong cation−π interaction between the ammonium of serotonin and the indole side chain of a tryptophan. However, the specific Trp used by MOD-1 is different from that used for 5-HT_3 (and the nAChR), aligning with a residue more than 40 amino acids distant in sequence space and on a different "loop" of the agonist binding site. This suggests a significant rearrangement of the ligand on binding these two closely related receptors. It is suggested that, unlike enzymes, receptors and other signaling molecules may need only to deliver an agonist to a general binding region, rather than establishing precise drug−receptor interactions.
Additional Information
© 2003 American Chemical Society. Received February 21, 2003. Publication Date (Web): May 16, 2003. This work was support by the NIH (NS-34407 and NS-11756). We thank Darren Beene for helpful discussion.Attached Files
Supplemental Material - ja0348086si20030415_012813.pdf
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Additional details
- Eprint ID
- 77328
- DOI
- 10.1021/ja0348086
- Resolver ID
- CaltechAUTHORS:20170510-080843497
- NIH
- NS-34407
- NIH
- NS-11756
- Created
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2017-05-16Created from EPrint's datestamp field
- Updated
-
2021-11-15Created from EPrint's last_modified field