Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/327281
Type: Artigo
Title: Combined Utilization Of H-1 Nmr, Ir, And Theoretical Calculations To Elucidate The Conformational Preferences Of Some L-histidine Derivatives
Author: Braga
Carolyne B.; Rittner
Roberto
Abstract: The conformational preferences of amino acids and their derivatives have been the subject of many investigations, because protein folding pathways that determine three-dimensional geometries are primarily restricted by the conformational space of each amino acid residue. Here we systematically describe the conformational behavior of L-histidine methyl ester (HisOMe) and its N-acetylated derivative (AcHisOMe) in the isolated phase and in solution. To this end, we employed spectroscopic techniques (H-1 NMR and IR), supported by quantum chemical calculations. Initially, the energetically favorable conformers, their energies, and structural properties obtained by density functional theory (DFT) and MollerPlesset perturbation theory (MP2) calculations in the isolated phase and in solution via the implicit solvation model IEF-PCM were presented. Next, experimental (3)J(HH) spinspin coupling constants obtained in different aprotic nonpolar and polar solvents were compared with the theoretically predicted ones for each conformer at the IEF-PCM/omega B97X-D/EPR-III level. A joint analysis of these data allowed the elucidation of the conformational preferences of the compounds in solution. Infrared data were also employed as a complement to estimate the HisOMe conformer populations. Finally, the quantum theory of atoms in molecules (QTAIM), the noncovalent interactions (NCI), and the natural bond orbitals (NBO) analyses were used to determine the intramolecular interactions that govern the relative conformational stabilities.
Subject: Quantum-chemical Calculations
Methyl-ester
Intramolecular Interactions
Density Functionals
Noncovalent Interactions
Thermochemical Kinetics
Nmr-spectroscopy
L-phenylalanine
L-tryptophan
Amino-acids
Editor: Amer Chemical Soc
Washington
Rights: fechado
Identifier DOI: 10.1021/acs.jpca.6b12515
Address: http://pubs-acs-org.ez88.periodicos.capes.gov.br/doi/abs/10.1021/acs.jpca.6b12515
Date Issue: 2017
Appears in Collections:Unicamp - Artigos e Outros Documentos

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