Acetylcholine Conformational Flexibility and Its Neutral Hydrolysis in Aqueous Solution

Author:

Fadilla Rizka N.12ORCID,Rusydi Febdian23ORCID,Madinah Roichatul24ORCID,Dipojono Hermawan K.5ORCID,Ahmad Faozan6ORCID,Mudasir Mudasir7ORCID,Puspitasari Ira28ORCID,Morikawa Yoshitada19ORCID

Affiliation:

1. Department of Precision Engineering Graduate School of Engineering Osaka University 2-1 Yamadaoka Suita Osaka 565-0871 Japan

2. Research Center for Quantum Engineering Design Faculty of Science and Technology Universitas Airlangga Jl. Mulyorejo Surabaya 60115 Indonesia

3. Department of Physics Faculty of Science and Technology Universitas Airlangga Jl. Mulyorejo Surabaya 60115 Indonesia

4. Department of Chemical Sciences Faculty of Science and Technology Universiti Kebangsaan Malaysia 43600 Bangi Selangor Malaysia

5. Advanced Functional Materials Research Group Department of Engineering Physics Faculty of Industrial Technology Institut Teknologi Bandung Jl. Ganesha no. 10 Bandung 40132 Indonesia

6. Department of Physics Faculty of Mathematics and Science IPB University Bogor 16680 Indonesia

7. Department of Chemistry Faculty of Mathematics and Natural Sciences Universitas Gadjah Mada Yogyakarta 55281 Indonesia

8. Information System Study Program Faculty of Science and Technology Universitas Airlangga Jl. Mulyorejo Surabaya 60115 Indonesia

9. Research Center for Precision Engineering Graduate School of Engineering Osaka University 2-1 Yamadaoka Suita 565-0871 Osaka Japan

Abstract

AbstractEnzymatic hydrolysis is the main target to deal with ACh depletion. However, a recent study indicates that the non‐enzymatic one may contribute to the depletion. This study highlights the necessity of considering possible conformers, discrete‐continuum models, and dispersive effects for investigating the neutral (non‐enzymatic) hydrolysis of flexible molecules in aqueous solution. We systematically built the possible conformers within the first‐principles framework. The results confirm the reactivity of high‐energy ACh conformer towards neutral hydrolysis. We proposed that conformational changes occur before the hydrolysis. The calculated activation and reaction energy shows that the discrete‐continuum solvation model gives the closest result to experimental observations. This study also shows that neglecting dispersive effects brings unreliable structures in the initial state, which leads to unreliable activation energy.

Publisher

Wiley

Subject

General Chemistry

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