NMR characterization of Tacrine in aqueous solution and insights into its interaction with amyloid-β_1-40 aggregates revealed by STD.

Authors

Matheus Yoshimitsu Tatsuta Nakamae, Paula S Rivero-Jerez, Anna Paola Butera, Fernando Macedo

Published in

Biophysical chemistry. Volume 340. Pages 107722. Oct 13, 2026. Epub Oct 13, 2026.

Abstract

The deposition of β-amyloid peptide (Aβ) aggregates in the brain is widely accepted as one of the major factors driving the development of Alzheimer's disease (AD). Tacrine (9-amino-1,2,3,4-tetrahydroacridine) is one of the most potent acetylcholinesterase inhibitors approved for the symptomatic treatment of AD, but its clinical use was discontinued due to hepatotoxicity. Recent studies have reported that tacrine can interact with Aβ and inhibit its aggregation, although the underlying mechanism is not yet fully elucidated, highlighting the need for detailed spectroscopic characterization under physiologically relevant conditions. Here, we report, to the best of our knowledge, the first complete and unambiguous assignment of the ¹H and ¹³C NMR resonances of tacrine in aqueous solution at near-physiological pH using a combination of ROESY, HSQC, and HMBC experiments. pH-dependent ¹HNMR studies revealed that aromatic proton resonances are highly sensitive to protonation state, displaying pronounced but fully reversible chemical-shift variations. The resulting spectral map provides a reliable basis for ligand-observed NMR investigations of tacrine and related compounds in aqueous media. Moreover, saturation transfer difference (STD)-NMR experiments were optimized to investigate the interaction of tacrine with soluble Aβ_1-40 aggregates. Under the optimized conditions, clear STD effects were observed exclusively in the presence of Aβ_1-40, confirming direct ligand-aggregate interaction. Differential saturation transfer among aromatic protons, particularly for H-7, suggests distinct proximity relationships within the tacrine- Aβ_1-40 complex. Together, these results establish a robust spectroscopic and methodological framework for future NMR studies of tacrine-based ligands and their interactions with amyloid assemblies.

PMID:
42913299
Bibliographic data and abstract were imported from PubMed on 24 Oct 2026.

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