The coordination between Al(III) and sialic acid (N-acetylneuraminic acid, HL, pKa = 2.58 ± 0.01) was studied by potentiometric titrations at 25 degrees in aqueous 0.2 M KCl, by 1H NMR, and by electrospray ionization mass spectrometry (ESI-MS). The potentiometric measurements gave the following aluminium complex stoichiometries and stability constants: log bAlLH-1+=-1:28 ± 0:01, logb(AlLH-2) = -6.34 ± 0.02, and logb(AlL2H-1) = -1.14 ± 0.04. The 1H NMR spectra yielded structural information on species AlLH-1+. The ESI-MS data confirmed the metal–ligand stoichiometry of the complexes. The metal–ligand speciation at micromolar Al(III) concentrations (i.e., under in vivo conditions) at physiological pH values reveals that considerable amount of Al(III) is complexed. This suggests that the toxic effect of Al(III) towards cellular membranes might be due to its coordination by protein-bound sialic acid.
The aluminium(III)-sialic acid interaction: A potential role in aluminium-induced cellular membrane degeneration
DI MARCO, VALERIO;BERTANI, ROBERTA;
2006
Abstract
The coordination between Al(III) and sialic acid (N-acetylneuraminic acid, HL, pKa = 2.58 ± 0.01) was studied by potentiometric titrations at 25 degrees in aqueous 0.2 M KCl, by 1H NMR, and by electrospray ionization mass spectrometry (ESI-MS). The potentiometric measurements gave the following aluminium complex stoichiometries and stability constants: log bAlLH-1+=-1:28 ± 0:01, logb(AlLH-2) = -6.34 ± 0.02, and logb(AlL2H-1) = -1.14 ± 0.04. The 1H NMR spectra yielded structural information on species AlLH-1+. The ESI-MS data confirmed the metal–ligand stoichiometry of the complexes. The metal–ligand speciation at micromolar Al(III) concentrations (i.e., under in vivo conditions) at physiological pH values reveals that considerable amount of Al(III) is complexed. This suggests that the toxic effect of Al(III) towards cellular membranes might be due to its coordination by protein-bound sialic acid.
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