Abstract
Serotonin is an essential mediator regulating diverse neural processes, and its deregulation is related to the development of debilitating neurological diseases. In particular, the human serotonin transporter (hSERT) is fundamental in completing the synaptic neural cycle by allowing reuptake of serotonin. Its inhibition is particularly attractive, especially as a pharmacological target against depressive syndrome. Here, we analyze, by using long-range molecular dynamic simulations, the behavior of a molecular photoswitch whose cis- and trans-isomers inhibit the hSERT differently. In particular, we evidence the structural and molecular basis behind the higher inhibiting capacity of the cis-isomer, which blocks more efficiently the hSERT conformational cycle, leading to serotonin uptake.
Original language | English |
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Pages (from-to) | 10333-10339 |
Number of pages | 7 |
Journal | The Journal of Physical Chemistry Letters |
Volume | 14 |
Issue number | 46 |
DOIs | |
Publication status | Published - 23 Nov 2023 |
Austrian Fields of Science 2012
- 104017 Physical chemistry
- 106045 Theoretical biology
Keywords
- Humans
- Biological Transport
- Molecular Dynamics Simulation
- Serotonin/metabolism
- Serotonin Plasma Membrane Transport Proteins/chemistry