Ab-initio study of pyrrole ring deformation in the indole group of 5-HT interacting with water molecules

Kei Odai*, Tohru Sugimoto, Etsuro Ito

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

5-Hydroxytryptamine (5-HT; serotonin) regulates metab-olism and various homeostatic mechanisms in the body, and is involved in depression. These complicated functions of 5-HT are supported by several 5-HT receptor and 5-HT transporter subtypes. The development of agonists/antagonists and activators/inhibitors of 5-HT receptors and transporters is a strong target for drug studies. Toward this purpose, we calculated the confor-mations and electrical states of ionized 5-HT in aqueous solution using ab-initio methods. When we assumed an ionized 5-HT molecule and three surrounding water molecules, the hydrogen bond network for these four molecules formed a ring shape, resulting in deformation of the pyrrole ring in the indole group of 5-HT. To our knowledge, this is the first finding demonstrating deformation of the indole skeleton. The findings suggest that the direct involvement of water in the binding between 5-HT and its receptors and transporters should be taken account when designing candidate 5-HT active compounds.

Original languageEnglish
Pages (from-to)127-131
Number of pages5
JournalBiophysics and physicobiology
Volume16
DOIs
Publication statusPublished - 2019

Keywords

  • 5-hydroxytryptamine
  • ab-initio calculation
  • optimization
  • self-consistent reaction field method

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Physiology
  • Biochemistry, Genetics and Molecular Biology (miscellaneous)

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