Capillary electrophoresis mass spectrometry coupling with immobilized enzyme electrospray capillaries
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
17376460
DOI
10.1016/j.chroma.2007.02.095
PII: S0021-9673(07)00425-6
Knihovny.cz E-zdroje
- MeSH
- biokompatibilní potahované materiály MeSH
- elektroforéza kapilární metody MeSH
- elektroforéza mikročipová MeSH
- elektrolyty MeSH
- enzymy imobilizované chemická syntéza klasifikace 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
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biokompatibilní potahované materiály MeSH
- elektrolyty MeSH
- enzymy imobilizované MeSH
- pepsin A MeSH
- proteiny MeSH
- trypsin 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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