Chip-based nLC-TOF-MS is a highly stable technology for large-scale high-throughput analyses |
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Authors: | L. Renee Ruhaak Sandra L. Taylor Suzanne Miyamoto Karen Kelly Gary S. Leiserowitz David Gandara Carlito B. Lebrilla Kyoungmi Kim |
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Affiliation: | 1. Department of Chemistry, University of California Davis, One Shields Avenue, Davis, CA, 95616, USA 2. Division of Biostatistics, Department of Public Health Sciences, University of California Davis, Davis, CA, 95616, USA 3. Division of Hematology and Oncology, University of California Davis Comprehensive Cancer Center, Sacramento, CA, 95817, USA 4. Division of Gynecologic Oncology, University of California Davis Comprehensive Cancer Center, Sacramento, CA, 95817, USA
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Abstract: | Many studies focused on the discovery of novel biomarkers for the diagnosis and treatment of disease states are facilitated by mass spectrometry-based technology. HPLC coupled to mass spectrometry is widely used; miniaturization of this technique using nano-liquid chromatography (LC)-mass spectrometry (MS) usually results in better sensitivity, but is associated with limited repeatability. The recent introduction of chip-based technology has significantly improved the stability of nano-LC-MS, but no substantial studies to verify this have been performed. To evaluate the temporal repeatability of chip-based nano-LC-MS analyses, N-glycans released from a serum sample were repeatedly analyzed using nLC-PGC-chip-TOF-MS on three non-consecutive days. With an average inter-day coefficient of variation of 4 %, determined on log10-transformed integrals, the repeatability of the system is very high. Overall, chip-based nano-LC-MS appears to be a highly stable technology, which is suitable for the profiling of large numbers of clinical samples for biomarker discovery. |
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