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A molecular container providing supramolecular protection against acetylcholine hydrolysis.
Lu, Yi-Long; Su, Jing; Li, Jian-Wei; Xu, Wen-Rong.
Affiliation
  • Lu YL; Key Laboratory of Advanced Materials of Tropical Island Resources of Ministry of Education, School of Chemistry and Chemical Engineering, Hainan University, Haikou 570228, PR China. xuwr2016@hainanu.edu.cn.
  • Su J; Key Laboratory of Advanced Materials of Tropical Island Resources of Ministry of Education, School of Chemistry and Chemical Engineering, Hainan University, Haikou 570228, PR China. xuwr2016@hainanu.edu.cn.
  • Li JW; MediCity Research Laboratory, University of Turku, Tykistökatu 6, FI-20520 Turku, Finland. jianwei.li@utu.fi.
  • Xu WR; Key Laboratory of Advanced Materials of Tropical Island Resources of Ministry of Education, School of Chemistry and Chemical Engineering, Hainan University, Haikou 570228, PR China. xuwr2016@hainanu.edu.cn.
Org Biomol Chem ; 22(8): 1634-1638, 2024 02 21.
Article in En | MEDLINE | ID: mdl-38323382
ABSTRACT
Alzheimer's disease (AD) is characterized by cognitive decline, often attributed to the deficiency of acetylcholine, which can undergo hydrolysis by acetylcholinesterase (AChE) within the biological milieu. Here, we report a supramolecular strategy that takes advantage of confinement effects to inhibit such a hydrolysis process, shedding some light on AD therapy. A water-soluble and bowl-shaped molecule, hexacarboxylated tribenzotriquinacene (TBTQ-C6), was employed to shield acetylcholine (G1) from enzymatic degradation through host-guest binding interactions. Our study revealed highly efficient host-guest interactions with a binding ratio of 1 3, resulting in a significant reduction in acetylcholine hydrolysis from 91.1% to 7.4% in the presence of AChE under otherwise identical conditions. Furthermore, TBTQ-C6 showed potential for attenuating the degradation of butyrylcholine (G2) by butyrylcholinesterase (BChE). The broader implications of this study extend to the potential use of molecular containers in various biochemical and pharmacological applications, opening new avenues for research in the field of neurodegenerative diseases.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Butyrylcholinesterase / Alzheimer Disease Limits: Humans Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Butyrylcholinesterase / Alzheimer Disease Limits: Humans Language: En Year: 2024 Type: Article