Molar Mass Profiling of Synthetic Polymers by Free-Solution Capillary Electrophoresis of DNA−Polymer Conjugates

• Published in: Analytical chemistry (Washington) Vol. 73; no. 8; pp. 1795 - 1803
• Main Authors: Vreeland, Wyatt N, Desruisseaux, Claude, Karger, Achim E, Drouin, Guy, Slater, Gary W, Barron, Annelise E
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 15.04.2001
• Subjects: Analysis; Applied sciences; capillary electrophoresis; Deoxyribonucleic acid; DNA; DNA - analysis; DNA - chemistry; Drag; Electrophoresis; Electrophoresis, Capillary; Exact sciences and technology; Fluorescence; Laser applications; Methods; Molecular Weight; Organic polymers; Physicochemistry of polymers; polyethylene glycol; Polyethylene Glycols - analysis; Polyethylene Glycols - chemistry; Polymerization; Polymers; Properties and characterization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Structure, morphology and analysis; Ethylene oxide polymer; Matrix isolation; Time of flight mass spectroscopy; Water soluble compound; Polydispersed polymer; Molecular weight distribution; Functionalization; Photoionization; Molecular weight determination; Capillary electrophoresis; Single stranded DNA; Laser desorption
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac001380+

The molar mass distribution of a polymer sample is a critical determinant of its material properties and is generally analyzed by gel permeation chromatography or more recently, by MALDI-TOF mass spectrometry. We describe here a novel method for the determination of the degree of polymerization of polydisperse, uncharged, water-soluble polymers (e.g., poly(ethylene glycol) (PEG)), based upon single-monomer resolution of DNA−polymer conjugates by free-solution capillary electrophoresis. This is accomplished by end-on covalent conjugation of a polydisperse, uncharged polymer sample (PEG) to a monodisperse, fluorescently labeled DNA oligomer, followed by electrophoretic analysis. The monodisperse, charged DNA “engine” confers to each conjugate an equal amount of electromotive force, while the varying contour lengths of the uncharged, polydisperse polymers engender different amounts of hydrodynamic drag. The balance of electromotive and hydrodynamic forces enables rapid, high-resolution separation of the DNA−polymer conjugates as a function of the size of the uncharged PEG tail. This provides a profile of the molar mass distribution of the original polymer sample that can be detected by laser-induced fluorescence through excitation of the dye-labeled DNA. We call this method free solution conjugate electrophoresis (FSCE). Theory-based analysis of the resulting electrophoresis data allows precise calculation of the degree of polymerization of the PEG portion of each conjugate molecule. Knowledge of the molecular mass of the uncharged polymer's repeat unit allows for direct calculation of the molar mass averages as well as sample polydispersity index. The results of these analyses are strikingly reminiscent of MALDI-TOF spectra taken of the same PEG samples. PEG samples of 3.4-, 5-, and 20-kDa nominal average molar mass were analyzed by FSCE and MALDI-TOF; the values of the molar mass averages, M w and M n, typically agree to within 5%. Measurements and molar mass calculations are performed without any internal standards or calibration. Moreover, when DNA−polymer conjugate analysis is performed in a chip-based electrophoresis system, separation is complete in less than 13 min. FSCE offers an alternative to MALDI-TOF for the characterization of uncharged, water-soluble polymers that can be uniquely conjugated to DNA.