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Pregled bibliografske jedinice broj: 1014244

Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution


Ramek, Michael; Marković, Marijana; Mutapčić, Ilina; Pejić, Jelena; Kelterer, Anne-Marie; Sabolović, Jasmina
Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution // ChemistryOpen, 8 (2019), 852-868 doi:10.1002/open.201900159 (međunarodna recenzija, članak, znanstveni)


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Naslov
Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution

Autori
Ramek, Michael ; Marković, Marijana ; Mutapčić, Ilina ; Pejić, Jelena ; Kelterer, Anne-Marie ; Sabolović, Jasmina

Izvornik
ChemistryOpen (2191-1363) 8 (2019); 852-868

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Amino acids ; Apical coordination ; Conformation analysis ; Density functional calculations ; EPR g tensor and hyperfine coupling

Sažetak
This study explores the structural properties and energy landscapes of the physiologically important bis(L‐asparaginato)copper(II) [Cu(L‐Asn)2] and (L‐histidinato)(L‐asparaginato)copper(II) [Cu(L‐His)(L‐Asn)]. The conformational analyses in the gas phase and implicitly modeled water medium, and magnetic parameters of electron paramagnetic resonance spectra were attained using density functional theory calculations. The apical CuII coordination and hydrogen bonding were analyzed. Predicted lower‐energy structures enabled the confirmation and, for apical bonding, also the refinement of structural proposals from literature. Available experimental results were indecisive regarding the amido‐group binding in the CuII equatorial plane in solutions, but the examination of the relative stability of Cu(L‐Asn)2 conformers in 30 binding modes confirms the glycine‐like mode as the most stable one. Previously reported experimental results for Cu(L‐His)(l‐Asn) were interpreted for l‐His to have a tridentate histamine‐like mode. However, the aqueous conformers with l‐His in the glycinato mode are also predicted to have low energies, which does not contradict the tridentate L‐His binding. The predicted magnetic parameters of conformers with an apical oxygen atom (intramolecular or from a water molecule) can reproduce the experimental data. An extent of conformational flexibility and abundance of L‐His‐containing ternary copper(II) amino acid complexes under physiological conditions may be related.

Izvorni jezik
Engleski



POVEZANOST RADA


Projekti:
HRZZ-IP-2014-09-3500 - Fiziološki i stereokemijski važni kompleksi bakra (II) s aminokiselinama: molekulsko modeliranje kombinirano s eksperimentalnim istraživanjima (CopperAminoAcidates) (Sabolović, Jasmina, HRZZ - 2014-09) ( CroRIS)

Poveznice na cjeloviti tekst rada:

doi onlinelibrary.wiley.com onlinelibrary.wiley.com

Citiraj ovu publikaciju:

Ramek, Michael; Marković, Marijana; Mutapčić, Ilina; Pejić, Jelena; Kelterer, Anne-Marie; Sabolović, Jasmina
Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution // ChemistryOpen, 8 (2019), 852-868 doi:10.1002/open.201900159 (međunarodna recenzija, članak, znanstveni)
Ramek, M., Marković, M., Mutapčić, I., Pejić, J., Kelterer, A. & Sabolović, J. (2019) Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution. ChemistryOpen, 8, 852-868 doi:10.1002/open.201900159.
@article{article, author = {Ramek, Michael and Markovi\'{c}, Marijana and Mutap\v{c}i\'{c}, Ilina and Peji\'{c}, Jelena and Kelterer, Anne-Marie and Sabolovi\'{c}, Jasmina}, year = {2019}, pages = {852-868}, DOI = {10.1002/open.201900159}, keywords = {Amino acids, Apical coordination, Conformation analysis, Density functional calculations, EPR g tensor and hyperfine coupling}, journal = {ChemistryOpen}, doi = {10.1002/open.201900159}, volume = {8}, issn = {2191-1363}, title = {Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution}, keyword = {Amino acids, Apical coordination, Conformation analysis, Density functional calculations, EPR g tensor and hyperfine coupling} }
@article{article, author = {Ramek, Michael and Markovi\'{c}, Marijana and Mutap\v{c}i\'{c}, Ilina and Peji\'{c}, Jelena and Kelterer, Anne-Marie and Sabolovi\'{c}, Jasmina}, year = {2019}, pages = {852-868}, DOI = {10.1002/open.201900159}, keywords = {Amino acids, Apical coordination, Conformation analysis, Density functional calculations, EPR g tensor and hyperfine coupling}, journal = {ChemistryOpen}, doi = {10.1002/open.201900159}, volume = {8}, issn = {2191-1363}, title = {Conformational Analyses of Physiological Binary and Ternary Copper(II) Complexes with L‐Asparagine and L‐Histidine ; Study of Tridentate Binding of Copper(II) in Aqueous Solution}, keyword = {Amino acids, Apical coordination, Conformation analysis, Density functional calculations, EPR g tensor and hyperfine coupling} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


Citati:





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