Eur. Phys. J. D (2012) 66: 121
https://doi.org/10.1140/epjd/e2012-20638-y

Regular Article

Systematic theoretical investigation of a positron binding to amino acid molecules using the ab initio multi-component molecular orbital approach

Quantum Chemistry DivisionYokohama City University, Seto 22-2, Kanazawa-ku, 236-0027 Yokohama Japan

^a e-mail: tachi@yokohama-cu.ac.jp

Received: 2 November 2011
Received in final form: 21 January 2012
Published online: 17 May 2012

Abstract

The feature of positron binding to twenty neutral amino acid molecules with the global minimum (GM) and intramoleculear hydrogen-bonded (HB) structures was analysed using the ab initio multi-component molecular orbital method. All amino acid molecules in the intramoleculear HB structures have positive positron affinity (PA, the binding energy of a positron) values, which means that a positron can be attached to parent molecules, while in the GM structures only three amino acid molecules of Gln, Trp, and His have positive PA values. Analysing the positronic orbitals of each positronic amino acid molecule and the electrostatic potential maps of the corresponding parent molecules, we found that long-range electrostatic interaction is the most crucial role in positron binding to neutral amino acid molecules. The strong correlation is observed between the PA and dipole moment, that is, a polar molecule with a large dipole moment has a large PA value. The critical dipole moment of neutral amino acid molecules for binding a positron was found at about 3.46 Debye. From the systematic analysis of twenty kinds of amino acid molecule, we theoretically confirmed the possibility of positron binding to conformers of amino acid molecules with strong dipole moment.