Gas phase copper(I) ion affinities of valine, lysine, and arginine based on the dissociation of Cu+-bound heterodimers at varying internal energies

Citation
Ba. Cerda et C. Wesdemiotis, Gas phase copper(I) ion affinities of valine, lysine, and arginine based on the dissociation of Cu+-bound heterodimers at varying internal energies, INT J MASS, 187, 1999, pp. 107-116
Citations number
38
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY
ISSN journal
13873806 → ACNP
Volume
187
Year of publication
1999
Pages
107 - 116
Database
ISI
SICI code
1387-3806(19990429)187:<107:GPCIAO>2.0.ZU;2-O
Abstract
The Cu+ affinities of the amino acids valine (Val), lysine (Lys), and argin ine (Arg) are determined in the gas phase based on the dissociations of Cu-bound dimers [A + B-i]Cu+, in which A represents one of the three amino ac ids studied and B-i a set of different amino acids of known Cu+ affinity (k inetic method). In order to deconvolute entropic contributions from experim entally measured free energies, the decompositions of [A + B-i]Cu+ are asse ssed as a function of internal energy using angle-resolved mass spectrometr y. The Cu+ affinities deduced for Val, Lys, and Arg are 283, 355, and 364 k J mol(-1), respectively. Lysine and arginine are found to have substantiall y larger entropies of Cu+ attachment when compared to valine. The combined affinity and entropy data are consistent with participation of the flexible side chain substituents of lysine and arginine in the coordination of Cu+, yielding multidentate complexes of markedly higher stability than the alip hatic amino acid valine. (Int J Mass Spectrom 185/186/187 (1999) 107-116) ( C) 1999 Elsevier Science B.V.