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Capillary electrophoresis mass spectrometry coupling with immobilized enzyme electrospray capillaries
J Krenkova, K Kleparnik, F Foret
Jazyk angličtina Země Nizozemsko
- MeSH
- biokompatibilní potahované materiály MeSH
- elektroforéza kapilární metody MeSH
- elektroforéza mikročipová MeSH
- elektrolyty MeSH
- enzymy imobilizované chemická syntéza klasifikace MeSH
- financování organizované MeSH
- hmotnostní spektrometrie s elektrosprejovou ionizací metody MeSH
- mikrochemie MeSH
- on-line systémy MeSH
- pepsin A metabolismus MeSH
- proteiny analýza chemie MeSH
- sekvenční analýza proteinů metody MeSH
- senzitivita a specificita MeSH
- studie proveditelnosti MeSH
- trypsin metabolismus MeSH
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 microm 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.
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- $a Capillary electrophoresis mass spectrometry coupling with immobilized enzyme electrospray capillaries / $c J Krenkova, K Kleparnik, F Foret
- 314 __
- $a Institute of Analytical Chemistry, Academy of Sciences of the Czech Republic, Veveri 97, 602 00 Brno, Czech Republic.
- 520 9_
- $a 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 microm 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.
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- $a elektrolyty $7 D004573
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- $a proteiny $x analýza $x chemie $7 D011506
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