4.6 Article

Capillary electrophoresis mass spectrometry coupling with immobilized enzyme electrospray capillaries

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1159, Issue 1-2, Pages 110-118

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2007.02.095

Keywords

capillary enzyme reactor; electrospray; mass spectrometry; capillary electrophoresis

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Open tubular capillary enzyme reactors were studied for rapid protein digestion and possible on-line integration into a CE/ESI/MS system. The need to minimize the time of the analyte molecules to diffuse towards the surface immobilized enzyme and to maximize the surface-to-volume (S/V) ratio of the open tubular reactors dictated the use of very narrow bore capillaries. Extremely small protein amounts (atto-femtomoles loaded) could be digested with enzymes immobilized directly on the inside wall of a 10 mu m I.D. capillary. Covalently immobilized L-1-tosylamido-2-phenylethyl chloromethyl ketone (TPCK)-trypsin and pepsin A were tested for the surface immobilization. The enzymatic activity was characterized in the flow-through mode with on-line coupling to electrospray ionization-time of flight-mass spectrometer (ESI/TOF-MS) under a range of protein concentrations, buffer pH's, temperatures and reaction times. The optimized reactors were tested as the nanospray needles for fast identification of proteins using CE-ESI/TOF-MS. (c) 2007 Elsevier B.V. All rights reserved.

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