Complexation of neurotransmitters ‒ dopamine, serotonin and melatonin ‒ with a DTPA-based cyclophane of high rigidity: 1H NMR shift and line-broadening

Ana Gabriela Arvízu-Santamaría, Rosa Elena Navarro, Yedith Soberanes, Enrique F. Velázquez, Hisila Santacruz, Motomichi Inoue

Research output: Contribution to journalArticlepeer-review

Abstract

The 1H NMR signals of the titled neurotransmitters undergo up-field shift accompanied by line-broadening in NMR titration with the DTPA-based cyclophane at pD 7.3; the cyclophane consists of a 4,4′-bis(1,1′-biphenyl-4,4′-dihydroxy)dianiline unit cyclised by a DTPA (diethylenetriaminepentaacetate) group through two amide linkages. Changes in chemical shifts of dopamine indicate the formation of a 1:1 complex with the formation constant K1 400 M−1; the complex of serotonin is likely to form a 2:1 host‒guest complex with β2 ≈ 105 M−2; melatonin does not form a complex with definite stoichiometry. The primary binding forces in the dopamine and serotonin complexes are electrostatic interaction between cationic neurotransmitter and anionic cyclophane molecules, and the resulting ionic pairs are stabilised by encapsulation. The electrostatic interaction is weakened by electrolytes; in 0.1 M Trizma buffer, dopamine does not yield a definite complex, and serotonin forms a 1:1 complex with K1 80 M−1. Extreme line-broadening of neurotransmitter signals suggests that the molecular motion of the guest molecule is slowed in the complex by interactions with the receptor molecule whose internal molecular motion is quenched partially. The high rigidity of the cyclophane enhances intermolecular interaction in the hydrophobic regions to prolong the lifetime of the complex.
Original languageSpanish (Mexico)
Pages (from-to)658-667
Number of pages10
JournalSupramolecular Chemistry
Volume29
Issue number9
DOIs
StatePublished - 2 Sep 2017
Externally publishedYes

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