期刊
ANALYTICAL CHEMISTRY
卷 72, 期 5, 页码 1015-1022出版社
AMER CHEMICAL SOC
DOI: 10.1021/ac991150z
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资金
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM015847, R37GM015847] Funding Source: NIH RePORTER
- NIGMS NIH HHS [GM 15847] Funding Source: Medline
A novel microfabricated device was implemented for facile coupling of capillary electrophoresis with mass spectrometry (CE/MS), The device was constructed from glass wafers using standard photolithographic/wet chemical etching methods. The design integrated (a) sample inlet ports, (b) the separation channel, (c) a liquid junction, and (d) a guiding channel for the insertion of the electrospray capillary, which was enclosed in a miniaturized subatmospheric electrospray chamber of an ion trap MS. The replaceable electrospray capillary was precisely aligned with the exit of the separation channel by a microfabricated guiding channel. No glue was necessary to seal the electrospray capillary. This design allowed simple and fast replacement of either the microdevice or the electrospray capillary. The performance of the device was tested for CE/MS of peptides, proteins, and protein tryptic digests. On-line tandem mass spectrometry was used for the structure identification of the protein digest products. High-efficiency/high-resolution separations could be obtained on a longer channel (11 cm on-chip) microdevice, and fast separations (under 50 s) were achieved with a short (4.5 cm on-chip) separation channel. In the experiments, both electrokinetic and pressure injections were used. The separation efficiency was comparable to that obtained from conventional capillary electrophoresis.
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