Journal of the American Society for Mass Spectrometry · 2016 · 94 citations · 37 references
PharmacyBiochemistryMolecular BiologyAnalytical ChemistryChromatographic AnalysisMass Spectrometric AnalysisChromatographyLiquid ChromatographyMass SpectrometryMobile Phase OptimizationMobile Phase SelectionStationary Phase ChemistryElectrospray IonizationLiquid Chromatography-mass SpectrometryLiquid Chromatography-mass Spectrometry AnalysisLiquid Chromatography-mass Spectrometry Method DevelopmentMass Spectrometry-compatible Mobile PhasesMobile Phase EffectsReversed-phase Mobile PhasesSolvent Optimization
Hexafluoroisopropanol (HFIP) has been widely used as an acidic modifier for mobile phases for liquid chromatography-mass spectrometry (LC-MS) analysis of oligonucleotides ever since the first report of its use for this purpose. This is not surprising, considering the exceptional performance of HFIP compared with carboxylic acids, which cause significant MS signal suppression in electrospray ionization. However, we have found that other fluorinated alcohols can also be utilized for mobile phase preparation and the choice of optimal fluorinated alcohol is determined by the ion-pairing (IP) agent. Although HFIP is a very good choice to be used alongside less hydrophobic IP agents, other fluorinated alcohols such as 1,1,1,3,3,3-hexafluoro-2-methyl-2-propanol (HFMIP) can significantly outperform HFIP when used with more hydrophobic IP agents. We also found that more acidic fluorinated alcohols assist with the transfer of oligonucleotides with secondary structure (e.g., folded strands and hairpins) into the gas phase. Graphical Abstract ᅟ.
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Ion mobility–mass spectrometry analysis of large protein complexes
Brandon T. Ruotolo, Justin L. P. Benesch, Alan M. Sandercock et al. · Nature Protocols · 2008 · 1.1K citations
Analysis of Oligonucleotides by HPLC−Electrospray Ionization Mass Spectrometry
Alex Apffel, John A. Chakel, Steven M. Fischer et al. · Analytical Chemistry · 1997 · 398 citations
Pharmacy, Biochemistry, Chemistry +16