期刊
JOURNAL OF CHROMATOGRAPHY A
卷 1218, 期 38, 页码 6732-6741出版社
ELSEVIER
DOI: 10.1016/j.chroma.2011.07.105
关键词
Retention prediction; Chemical identification; Isocratic to gradient conversion; Retention projection; Gradient profile; Cross-instrument
资金
- National Science Foundation [IOS-0923960, MCB-0725149]
- Minnesota Agricultural Experiment Station
- Gordon and Margaret Bailey Endowment for Environmental Horticulture
- Direct For Biological Sciences
- Div Of Molecular and Cellular Bioscience [0725149] Funding Source: National Science Foundation
Using current data analysis techniques, even the most advanced LC-MS instrumentation can identify only a small fraction of compounds found in typical biological extracts. Augmenting MS information with HPLC retention information allows many more to be identified. In fact, our calculations indicate that a quadrupole MS is able to identify more compounds than an FTICR-MS when the quadrupole spectrum is augmented with retention information. Unfortunately, retention information is extremely difficult to harness for compound identification. Here, we demonstrate the first use of isocratic data measured on one LC-MS to project gradient retention on to different LC-MS systems. Using 35 chemically diverse solutes chosen to encompass the full range of reversed-phase alkylsilica interactions, and using experimental conditions typical of metabolomics experiments, gradient retention was projected from one instrument to another with only 1.2-2.6% error-enough accuracy to considerably improve compound identification. Besides accounting for nonlinear relationships of retention versus solvent composition as well as dead time versus solvent composition, accounting for the precise shape of the gradient profile (not just the dwell volume) improved projection accuracy on one instrument by up to 4 fold whereas flow rate non-idealities likely caused considerable error on the other instrument. Thus, these two factors must be taken into account to accurately project retention on diverse instrumentation. (C) 2011 Elsevier B.V. All rights reserved.
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