Journal
JOURNAL OF PROTEOME RESEARCH
Volume 8, Issue 5, Pages 2397-2406Publisher
AMER CHEMICAL SOC
DOI: 10.1021/pr8010205
Keywords
Adrenal gland; Chemometrics; MCR-ALS; MPCA; HRMAS H-1 NMR spectroscopy; Kidney; Liver; Intact tissue; Metabonomics; Pancreas; PARAFAC; PCA; Plasma
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Multicompartmental metabolic profiling combined with multivariate data analysis offers a unique opportunity to explore the multidimensional metabolic relationships between various biological matrices. Here, we applied unsupervised chemometric methods for integrating H-1 NMR metabolic profiles from mouse plasma, liver, pancreas, adrenal gland and kidney cortex matrices in order to infer intercompartments functional links. Principal Component Analysis (PCA) revealed metabolic differences between matrices but contained limited information on intercompartment metabolic relationships. Multiway PCA enabled the assessment of interindividual metabolic variability across multiple compartments in a single model and, therefore, metabolic correlations between different organs and circulating biofluids. However, this approach does not provide information on the relative contribution of one compartment to another. Integration of metabolic profiles using Multivariate Curve Resolution (MCR) and Parallel Factor Analysis (PARAFAC) methods provided an overview of functional relationships across matrices and enabled the characterization of compartment-specific metabolite signatures, the spectrotypes. In particular, the spectrotypes describe biochemical profiles specific or common to different biological compartments. Consequently, MCR-ALS and PARAFAC appeared to be better adapted for stepwise variable and compartment selection for further correlation analysis. Such a combination of chemometric techniques could provide new research avenues to assess the efficacy of drug or nutritional interventions on targeted organs.
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