- Short Report
- Open Access
A short update on the structure of drug binding sites on neurotransmitter transporters
© Ravna et al; licensee BioMed Central Ltd. 2011
Received: 15 August 2011
Accepted: 22 December 2011
Published: 22 December 2011
The dopamine (DAT), noradrenalin (NET) and serotonin (SERT) transporters are molecular targets for different classes of psychotropic drugs. Cocaine and the SSRI (S)-citalopram block neurotransmitter reuptake competitively, but while cocaine is a non-selective reuptake inhibitor, (S)-citalopram is a selective SERT inhibitor.
Here we present comparisons of the binding sites and the electrostatic potential surfaces (EPS) of DAT, NET and SERT homology models based on two different LeuTAa templates; with a substrate (leucine) in an occluded conformation (PDB id 2a65), and with an inhibitor (tryptophan) in an open-to-out conformation (PDB id 3f3a). In the occluded homology models, two conserved aromatic amino acids (tyrosine and phenylalanine) formed a gate between the putative binding pockets, and this contact was interrupted in the open to out conformation. The EPS of DAT and NET were generally negative in the vestibular area, whereas the EPS of the vestibular area of SERT was more neutral.
The findings presented here contribute as an update on the structure of the binding sites of DAT, NET and SERT. The updated models, which have larger ligand binding site areas than models based on other templates, may serve as improved tools for virtual ligand screening.
There are three main dopaminergic pathways in the brain, the mesolimbic/mesocortical pathway involved in emotion- and drug-induced reward systems, the nigrostriatal pathway involved in motor control, and the tuberohypophyseal neurons involved in regulation of secretions from pituitary gland. The reward system is linked to drug abuse, and it is activated when a person receives positive reinforcement for certain behaviors, which can be artificial rewards (addictive drugs) or natural rewards (sex or food). When cocaine binds to DAT, a "reward" associated with an elevated dopamine concentration in the synapse in the Nucleus Accumbens occurs . Individuals with the hypodopaminergic trait involving an impairment of the reward cascade ("Brain Reward Cascade Model") termed "Reward Deficiency syndrome" (RDS), which may be due to several genes, and also due to environmental stimuli, have higher risk for substance abuse, impulsive behavior, eating bingeing, pathological gambling, ADHD and sex addiction etc. [2, 3].
Cocaine has similar binding affinities for DAT and the noradrenalin (NET) and serotonin (SERT) transporters. In addition to stimulant action, NET and SERT are molecular targets for antidepressants (selective serotonin reuptake inhibitors (SSRIs), selective noradrenaline reuptake inhibitors (NERI), serotonin-noradrenalin reuptake inhibitors (SNRI), and tricyclic antidepressants (TCA)). Binding studies have demonstrated that SSRIs are from 300 to 3,500 times more selective for SERT over NET, and generally have low affinities for DAT .
DAT, NET and SERT belong to the large neurotransmitter: sodium symporter (NSS) family of transporters , and they regulate monoamine concentrations at neuronal synapses by carrying monoamines across neuronal membranes into presynaptic nerve cells, using an inwardly directed sodium gradient as an energy source. Cocaine elevates the concentration of all three neurotransmitters at synapses, while SSRIs and NERIs elevate the concentration of serotonin and noradrenaline, respectively. Both serotonergic and noradrenergic neurons are localized in the pons and medulla (raphe nuclei), and their axons project to brain regions such as the limbic system, the cerebral cortex and hypothalamus.
Structural information about DAT, SERT and NET and their drug interactions is important for understanding their molecular mechanisms of action, and provide useful tools for new drug discovery. Elucidating differences in binding site conformations of occluded and open-outward neurotransmitter transporter models, and investigating differences in the electrostatic potential surfaces of the three transporters, may give insight into binding modes of drugs in different conformations and to the different transporters. No X-ray crystal structures of mammalian human DAT, SERT or NET have been reported, but several Aquifex aeolicus LeuTAa crystal structures have been published [6–8]. LeuTAa is a bacterial homologue of DAT, SERT and NET that is regarded as suitable template for molecular models of these transporters. The sequence identity between LeuTAa and DAT, NET and SERT is ~20% .
In present study, we have used the crystal structure of LeuTAa, complexed with an inhibitor (tryptophan) in an open-to-out conformation  (PDB id 3f3a) as a template for molecular modeling of DAT, SERT and NET. We have compared the binding site conformations of the models with the binding site conformations of our previous DAT, SERT and NET models  that were based on the crystal structure of LeuTAa, complexed with a substrate (leucine) in an occluded conformation  (PDB id 2a65). Molecular models of DAT, NET and SERT were constructed using the ICM version 3.6 . The modeling procedure of DAT, NET and SERT based on LeuTAa in the occluded conformation  has previously been described in . A comprehensive amino acid sequence alignment  of all known prokaryotic and eukaryotic neurotransmitter: sodium symporter (NSS) proteins including DAT, NET and SERT, was used as input alignment. In the ICM homology modeling module, the model is constructed from a few core sections defined by the average of Cα atom positions in the conserved regions. Loops are searched for within several thousand high quality three dimensional (3D) protein structures by matching them with regard to sequence similarity and steric interactions with the surroundings of the model. The best fitting loop is selected by calculating the maps around the loops and scoring them based on their relative energies.
The models were refined by globally optimizing side-chain positions and annealing of the backbones using the RefineModel macro of ICM. This macro included (1) a Monte Carlo simulation  of side chains, (2) five steps of iterative annealing of the backbone structure, and (3) a second Monte Carlo simulation of side chains. In step 1 of the RefineModel macro, a side-chain conformational analysis using the "MonteCarlo fast" option of the ICM global optimization procedure for sampling of the conformational space of a molecule, is performed . Iterative random movements, followed by local energy minimizations, and by a complete energy calculation, were performed, and each iteration was accepted or rejected based on energy and temperature criteria. Step 2 performed an iterative annealing of the backbone with provided tethers, which are harmonic restraints pulling an atom in the model to a static point in space represented by a corresponding atom in the template. A second Monte Carlo side-chain sampling was performed in step 3.
The ICM PocketFinder algorithm, which detects cavities of sufficient size to bind ligands,  was used to detect putative drug binding pockets in the DAT, NET and SERT models. A tolerance level of 3 was used, thus cavities with a volume greater than 3 Å3 were considered. The reason for choosing a tolerance level of 3, instead of the default tolerance level of 4.6, is that a larger area is detected as a binding pocket. The algorithm, which uses a transformation of the Lennard-Jones potential calculated from a three-dimensional protein structure, does not require any knowledge about a potential ligand molecule. Thus, the ICM PocketFinder algorithm is based solely on protein structure . The detected putative drug binding pockets were compared with detected putative drug binding pockets in DAT, NET and SERT in occluded conformation .
Results and discussion
Amino acids reported by ICM PocketFinder to contribute to the binding pockets of open-to-out DAT, NET and SERT
F76, A77, D79, L80 A81, W84, R85, Y88
F72, A73, D75, L76, A77, W80, R81, Y84
Y95, A96, D98, G100, W103, R104, Y107, I108
V152, F155, Y156, I159
145, V148, Y151, Y152, I155, W158
A169, I172, A173, Y175, Y176, I179, W182
F320, S321, G323, F326, V328
F317, S318, G320, F323, V325
F335, L336, L337, G338, F341, V343
V382, A383, K384, D385, G386, P387, L389, I390
A380, E382, G383, A384, L386, V387, F388
A398, K399, D400, A401, P403, L405, L406, F407
S422, A423, G426
S419, S420, G423
F472, D476, A480
G465, I466, L469, T470
The stereochemical qualities of the models were checked using the Structural Analysis and Verification Server (SAVS) http://nihserver.mbi.ucla.edu/SAVS/. Programs run on SAVS, which examine the stereochemical quality of a protein structure by analyzing its overall and residue-by-residue geometry, were Procheck , What_check , and Errat . The overall quality factors of the DAT, NET and SERT models were 90.0, 93.7 and 87.6, respectively. The DAT model Ramachandran plot revealed that 93.8% of the residues were in the most favored regions, 5.9% were in additional allowed regions, 0.3% were in generously allowed regions, and 0.0% were in disallowed regions. The Ramachandran plot of NET reported 93.7% (most favored regions), 6.1% (additional allowed regions), 0.3% (generously allowed regions), and 0.0% (disallowed regions), and the Ramachandran plot of SERT reported 94.0% (most favored regions), 6.0% (additional allowed regions), 0.0% (generously allowed regions), and 0.0% (disallowed regions). All three models were satisfactory according to What_check.
The ligand binding site areas of our previous DAT, NET and SERT models  were tighter, possibly resulting in a greater chance of sterical hindrance for docked ligands. The updated models presented in this short report, which have larger ligand binding site areas than models based on other templates, may serve as improved tools for virtual ligand screening.
Co-ordinates of the DAT, NET and SERT models are available from the authors upon request.
This work was supported by a grant from the Nevronor program of the Research Council of Norway (project 176956), by the Polish-Norwegian Research Fund (grant PNRF-103-A1-1/07).
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