Effect of the basic residue on the energetics and dynamics of dissociation of phosphopeptides

• Published in: International journal of mass spectrometry Vol. 330-332; pp. 295 - 301
• Main Authors: Laskin, Julia, Kong, Ricky P.W., Song, Tao, Chu, Ivan K.
• Format: Journal Article
• Language: English
• Published: United States Elsevier B.V 15.12.2012
• Subjects: Activation entropy; Environmental Molecular Sciences Laboratory; Kinetics; Phosphorylated peptide; RRKM modeling; Surface-induced dissociation (SID); Threshold energy; Activation entropy; RRKM modeling; Phosphorylated peptide; Kinetics; Threshold energy; Surface-induced dissociation (SID)
• ISSN: 1387-3806; 1873-2798
• DOI: 10.1016/j.ijms.2012.09.013

[Display omitted] ► We examined energy and entropy effects in dissociation of protonated peptides containing phosphoserine using surface-induced dissociation combined with RRKM modeling. ► Different kinetics for H3PO4 loss from phosphoserine were observed under the mobile proton and nonmobile proton condition. ► The loss of H3PO4 from phosphoserine is a two-step process. ► In the presence of a basic residue, the phosphate abstraction from the phosphorylated side chain is followed by dissociation of the ion–molecule complex. ► The relative rate constants of the two steps determine the observed kinetics. Time- and collision-energy-resolved surface-induced dissociation (SID) of protonated peptides containing phosphoserine (s) was studied using a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer configured for SID experiments. We examined fragmentation of three singly protonated peptides: GGGsGGG, KGGsGGG and RGGsGGG. Fragmentation of GGGsGGG occurs under the mobile proton condition, while the ionizing proton is sequestered by the basic residue, resulting in the nonmobile proton condition in dissociation of the two basic peptides: KGGsGGG and RGGsGGG. RRKM modeling of the experimental data demonstrates that the energetics and dynamics of H3PO4 loss are different under mobile and nonmobile proton conditions. Specifically, fragmentation of GGGsGGG is characterized by a higher dissociation barrier, 1.68eV, and higher activation entropy, 11e.u. (e.u.=entropy unit), than fragmentation of the basic peptides. Similar threshold energies of 1.36eV and 1.40eV and activation entropies of −4.9e.u. and 0.3e.u. were obtained for KGGsGGG and RGGsGGG, respectively. We propose that the loss of H3PO4 from phosphoserine is a two-step process, in which the phosphate abstraction from the phosphorylated side chain is followed by dissociation of the ion–molecule complex.