RT Journal Article SR Electronic T1 Peptide Inhibitors Disrupt the Serotonin 5-HT2C Receptor Interaction with Phosphatase and Tensin Homolog to Allosterically Modulate Cellular Signaling and Behavior JF The Journal of Neuroscience JO J. Neurosci. FD Society for Neuroscience SP 1615 OP 1630 DO 10.1523/JNEUROSCI.2656-12.2013 VO 33 IS 4 A1 Noelle C. Anastasio A1 Scott R. Gilbertson A1 Marcy J. Bubar A1 Anton Agarkov A1 Sonja J. Stutz A1 Yowjiun Jeng A1 Nicole M. Bremer A1 Thressa D. Smith A1 Robert G. Fox A1 Sarah E. Swinford A1 Patricia K. Seitz A1 Marc N. Charendoff A1 John W. Craft, Jr A1 Fernanda M. Laezza A1 Cheryl S. Watson A1 James M. Briggs A1 Kathryn A. Cunningham YR 2013 UL http://www.jneurosci.org/content/33/4/1615.abstract AB Serotonin (5-hydroxytryptamine; 5-HT) signaling through the 5-HT2C receptor (5-HT2CR) is essential in normal physiology, whereas aberrant 5-HT2CR function is thought to contribute to the pathogenesis of multiple neural disorders. The 5-HT2CR interacts with specific protein partners, but the impact of such interactions on 5-HT2CR function is poorly understood. Here, we report convergent cellular and behavioral data that the interaction between the 5-HT2CR and protein phosphatase and tensin homolog (PTEN) serves as a regulatory mechanism to control 5-HT2CR-mediated biology but not that of the closely homologous 5-HT2AR. A peptide derived from the third intracellular loop of the human 5-HT2CR [3L4F (third loop, fourth fragment)] disrupted the association, allosterically augmented 5-HT2CR-mediated signaling in live cells, and acted as a positive allosteric modulator in rats in vivo. We identified the critical residues within an 8 aa fragment of the 3L4F peptide that maintained efficacy (within the picomolar range) in live cells similar to that of the 3L4F peptide. Last, molecular modeling identified key structural features and potential interaction sites of the active 3L4F peptides against PTEN. These compelling data demonstrate the specificity and importance of this protein assembly in cellular events and behaviors mediated by 5-HT2CR signaling and provide a chemical guidepost to the future development of drug-like peptide or small-molecule inhibitors as neuroprobes to study 5-HT2CR allostery and therapeutics for 5-HT2CR-mediated disorders.