Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 18 von 30

Details

Autor(en) / Beteiligte
Titel
Utilizing Microchip Capillary Electrophoresis Electrospray Ionization for Hydrogen Exchange Mass Spectrometry
Ist Teil von
  • Analytical chemistry (Washington), 2015-06, Vol.87 (12), p.6280-6287
Ort / Verlag
United States: American Chemical Society
Erscheinungsjahr
2015
Quelle
MEDLINE
Beschreibungen/Notizen
  • Hydrogen exchange (HX) mass spectrometry (MS) of complex mixtures requires a fast, reproducible, and high peak capacity separation prior to MS detection. The current paradigm relies on liquid chromatography (LC) with fast gradients performed at low temperatures to minimize back exchange. Unfortunately, under these conditions, the efficiency of LC is limited due to resistance to mass transfer, reducing the capability to analyze complex samples. Capillary electrophoresis (CE), on the other hand, is not limited by resistance to mass transfer, enabling very rapid separations that are not adversely affected by low temperature. Previously, we have demonstrated an integrated microfluidic device coupling CE with electrospray ionization (ESI) capable of very rapid and high efficiency separations. In this work, we demonstrate the utility of this microchip CE-ESI device for HX MS. High speed CE-ESI of a bovine hemoglobin pepsin digestion was performed in 1 min with a peak capacity of 62 versus a similar LC separation performed in 7 min with peak capacity of 31. A room temperature CE method performed in 1.25 min provided similar deuterium retention as an 8.5 min LC method conducted at 0 °C. Separation of a complex mixture with CE was done with considerably better speed and nearly triple the peak capacity than the equivalent separation by LC. Overall, the results indicate the potential utility of microchip CE-ESI for HX MS.
Sprache
Englisch
Identifikatoren
ISSN: 0003-2700
eISSN: 1520-6882
DOI: 10.1021/acs.analchem.5b01179
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4470751

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX