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Zwitterionic structures of selenocysteine-containing dipeptides and their interactions with Cu(II) ions

Gunajyoti Das and Shilpi Mandal

Department of Chemistry, North Eastern Hill University, Shillong-793022, India

 

E-mail: guna_das78@yahoo.co.in

Abstract: The molecular structures of a series of selenocysteine-containing dipeptides in their zwitterionic forms were studied using the B3LYP/6-311++G(d,p) level in the aqueous phase. The B3LYP and BHandHLYP functionals in combination with 6-311++G(d,p) and LANL2DZ basis sets were used to investigate the effects of metal coordination on the structural and molecular properties of the dipeptides by complexing them with bivalent copper ions. The results from this DFT study provide valuable insights into the interaction enthalpies (metal ion-binding affinities) and free energies, the influence of the C-terminal moiety on the backbone structural features, the existence of various types of intramolecular H-bond interactions, harmonic vibrational frequencies, along with various other electronic properties pertaining to the zwitterions of the dipeptide molecules as well as their metallic complexes. Metal coordination via the carboxylate groups tends to enhance the planarity of the amide planes. The participations of the N- and C-terminal side-chain moieties in metal-binding markedly enhance the thermodynamic stability of the metalated dipeptides. The theoretical λmax values, calculated using the TD/DFT level for all the systems, well represent the occurrence of d-d transitions in the Cu-dipeptide complexes

Keywords: selenocysteine – zwitterionic dipeptides – interactions – with Cu(II) ions – vibrational frequencies – theoretical λmax values

Full paper is available at www.springerlink.com.

DOI: 10.1515/chempap-2015-0064

 

Chemical Papers 69 (4) 616–626 (2015)

Tuesday, May 11, 2021

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