Improved mass spectrometric detection of acidic peptides by variations in the functional group pKa values of reverse micelle extraction agents. Issue 6 (22nd February 2018)

• Record Type: Journal Article
• Authors: Zhao, Bo; Serrano, Mahalia A. C.; Wang, Meizhe; Liu, Tianying; Gordon, Mallory R.; Thayumanavan, S.; Vachet, Richard W.
• Is Part Of: Analyst. Volume 143:Issue 6(2018)
• Page Start: 1434
• Page End: 1443
• Publication Date: 2018-02-22
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/c7an02094e
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : Functional groups in reverse micelles maintain their aqueous phase p K a and allow selective extraction of peptides according to isoelectric point. Abstract : Polymeric reverse micelles can be used to selectively extract peptides from complex mixtures via a two-phase extraction approach. In previous work, we have shown that the charge polarity of the hydrophilic functional group that is in the interior of the reverse micelle dictates the extraction selectivity. To investigate how the extraction is influenced by the inherent p K a of the functional group, we designed and tested a series of polymeric reverse micelles with variations in the hydrophilic functional group. From this series of polymers, we find that the extraction capability of the reverse micelles in an apolar phase is directly related to the aqueous phase p K a of the interior functional group, suggesting that the functional groups maintain their inherent chemistry even in the confined environment of the reverse micelle interior. Because these functional groups maintain their inherent p K a in the reverse micelle interior, they provide predictable extraction selectivity upon changes in aqueous phase pH. We exploit this finding to demonstrate that sulfonate-containing polymers can be used to remove basic peptides from complex mixtures, thereby allowing the improved detection of acidic peptides. Using these new materials, we also demonstrate a new means of isoelectric point (pI) bracketing that allows the mass spectrometric detection of peptides with a defined and narrow range of pI values.