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pH-dependent X-ray Photoelectron Chemical Shifts and Surface Distribution of Cysteine in Aqueous Solution.
Carravetta, Vincenzo; de Abreu Gomes, Anderson Herbert; Monti, Susanna; Mocellin, Alexandra; Marinho, Ricardo R T; Björneholm, Olle; Ågren, Hans; Naves de Brito, Arnaldo.
Afiliación
  • Carravetta V; Institute of Chemical and Physical Processes , CNR-IPCF , via G. Moruzzi 1 , I-56124 Pisa , Italy.
  • de Abreu Gomes AH; Department of Applied Physics, Institute of Physics "Gleb Wataghin" , University of Campinas , 13.083-859 Campinas , SP , Brazil.
  • Monti S; Institute of Chemistry of Organometallic Compounds , CNR-ICCOM , via G. Moruzzi 1 , I-56124 Pisa , Italy.
  • Mocellin A; Institute of Physics , Brasilia University , Box 4455, Brasília 70910-970 , Brazil.
  • Marinho RRT; Institute of Physics , Brasilia University , Box 4455, Brasília 70910-970 , Brazil.
  • Björneholm O; Institute of Physics , Federal University of Bahia , 40.170-115 , Salvador , BA , Brazil.
  • Ågren H; Department of Physics and Astronomy , Uppsala University , 752 36 Uppsala , Sweden.
  • Naves de Brito A; Department of Physics and Astronomy , Uppsala University , 752 36 Uppsala , Sweden.
J Phys Chem B ; 123(17): 3776-3785, 2019 05 02.
Article en En | MEDLINE | ID: mdl-30964991
ABSTRACT
The distribution and protonation states of amino acids in water droplets are of considerable concern in studies on the formation of clouds in the atmosphere as well as in many biological contexts. In the present work we use the amino acid cysteine as a prototypical example and explore the protonation states of this molecule in aqueous solution, which are strongly affected by the acidity of the environment and also can show different distributions between surface and bulk. We use a combination of X-ray photoelectron chemical shift measurements, density functional theory calculations of the shifts, and reactive force field molecular dynamics simulations of the underlying structural dynamics. We explore how the photoelectron spectra distinctly reflect the different protonation states that are generated by variation of the solution acidity and how the distribution of these protonation states can differ between bulk and surface regions. At specific pH values, we find that the distribution of the cysteine species at the surface is quite different from that in bulk, in particular, for the appearance in the surface region of species which do not exist in bulk. Some ramifications of this finding are discussed.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Phys Chem B Asunto de la revista: QUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Phys Chem B Asunto de la revista: QUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Italia
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