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Amazing Stability of Phosphate-Quaternary Amine Interactions
Author(s) -
Amina S. Woods,
Susan C. Moyer,
Shelley N. Jackson
Publication year - 2008
Publication title -
journal of proteome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.644
H-Index - 161
eISSN - 1535-3907
pISSN - 1535-3893
DOI - 10.1021/pr8001595
Subject(s) - chemistry , protein quaternary structure , covalent bond , non covalent interactions , mass spectrometry , dissociation (chemistry) , electrospray ionization , infrared multiphoton dissociation , molecule , amine gas treating , ammonium , phosphate , combinatorial chemistry , hydrogen bond , organic chemistry , chromatography , biochemistry , protein subunit , gene
We have previously used MALDI mass spectrometry to highlight ammonium- or guanidinium-aromatic interactions via cation-pi bonding and ammonium- or guanidinium-phosphate interactions through salt bridge formation. In the present work, the gas-phase stability and dissociation pathways of the interaction between phosphorylated peptides and compounds containing quaternary amines are demonstrated using electrospray ionization mass spectrometry. The presence of one quaternary amine in a compound is enough to form a noncovalent complex with a phosphorylated residue. However, if two quaternary amines are present in one molecule, the electrostatic interactions of the quaternary amines with the phosphate results in a "covalent-like" stability, and these bonds can withstand fragmentation by collision-induced dissociation at energies similar to those that fragment covalent bonds. Such interactions are important in accounting for physiological, pathophysiological, and pharmacological effects of many therapeutic compounds and small molecules containing quaternary amines or phosphates.

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