Premium
Proton affinity ladder for uridine and analogs: influence of the hydroxyl group on the sugar ring conformation
Author(s) -
Mezzache S.,
Alves S.,
Pepe C.,
Quelquejeu M.,
Fournier F.,
Valery J.M.,
Tabet J.C.
Publication year - 2005
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/jms.844
Subject(s) - chemistry , protonation , substituent , stereochemistry , ring (chemistry) , furanose , nucleoside , alkane stereochemistry , glycosidic bond , crystallography , crystal structure , ion , enzyme , organic chemistry
A ladder of relative proton affinities ( PA ) for a series of modified uridines (e.g. araU, ddU, 5BrU, 5BrdU and 5IU) was established from competitive dissociations of proton‐bound heterodimers using Cooks and co‐workers' kinetic method. The studied heterodimers are constituted of a modified nucleoside and either an amino acid or a nucleoside with known PA value. These non‐covalent heterodimers were prepared under electrospray conditions to be selected and dissociated into the ion‐trap analyzer. These results allowed our PA ladder of uridine and deoxyuridine analogs substituted at the C‐5 position in the uracil ring to be extended. From this scale, it was showed that the substitution of hydrogen atom at the C‐2′ position in the sugar ring by a hydroxyl group involves a decrease of about 7 kJ mol −1 . The experimental values for U, 5MeU, dU, 5MedU, ddU and araU are consistent with those obtained by DFT calculations (B3P86/6–31+G*//B3LYP/6–31G*). Several neutral and protonated conformations of these compounds were considered, in particular the ring conformation of furanose and the orientation of the base with respect to the sugar ring. These calculated results showed the influence of sugar substituent on the conformation of the neutral form of theses nucleosides. However, the most stable protonated structure is the same for all the studied nucleosides except for araU, where the position of the anti 2′‐OH group imposes a specific conformation. Copyright © 2005 John Wiley & Sons, Ltd.