ChemRxiv
February 7, 2023
Vito F. Palmisano, Claudio Agnorelli, David Erritzøe et al.
1 citation
Classic psychedelics target the 5-HT2A serotonin receptor, but their precise mode of action remains unclear. Computational modeling of the receptor's orthosteric binding pocket for several psychedelics—including serotonin, LSD, DMT, and a photoswitchable analog (AzoDMT)—revealed two nearly equivalent binding poses. LSD and serotonin preferred the canonical crystallized pose, whereas DMT and 4-OH-DMT slightly favored a newly identified pose. The cis form of AzoDMT was the most stable, and its azobenzene domain interacted with the same residue (L229) responsible for LSD's extracellular loop closure. These simulations clarify drug–protein interactions and may aid development of new psychedelic compounds.
ACS Chemical Neuroscience
February 18, 2026
Vito F. Palmisano, Micaela Vidal−sánchez, Juan J. Nogueira
Bulky substitutions on the N-benzyl ring of 25CN-NBx compounds cause a significant shift in the position of W336, a key toggle switch residue in the 5-HT2A receptor. This shift influences receptor activation and is thought to play a crucial role in mediating psychedelic signaling. Potential of mean force calculations along the toggle switch's dihedral angle confirm this result. End-state free energy calculations show that 25CN-NB-2-OH-3-Me and 25CN-NB-2-OH-5-MeO have the highest and lowest affinities, respectively, for the receptor. When W336 adopts its negative dihedral state, it establishes stronger van der Waals interactions with residues F332 and I163, key players in receptor activation. This framework can extend to other G protein-coupled receptors where the toggle switch is central to signal activation.
January 22, 2025
Vito F. Palmisano
The development of new treatments for neuropsychiatric disorders has been slow, but the psychedelic renaissance offers promising therapeutic avenues that may reduce side effects and eliminate the need for chronic antidepressant use. A key goal is understanding how altered states of consciousness contribute to antidepressant effects, requiring tools to selectively activate specific neural populations. Photopharmacology, using external stimuli to control photoactive compounds with precision and minimal toxicity, is a compelling approach. This thesis uses computational methods—including molecular dynamics, enhanced sampling, quantum mechanics/molecular mechanics, and quantum mechanics—to study 5-HT2A receptor agonists' binding, membrane permeability, and photophysical properties, aiming to advance innovative therapies.