Next Article in Journal
Monitoring for Response to Antineoplastic Drugs: The Potential of a Metabolomic Approach
Next Article in Special Issue
Dynamics of Monoterpene Formation in Spike Lavender Plants
Previous Article in Journal
Metabolomic Modularity Analysis (MMA) to Quantify Human Liver Perfusion Dynamics
Previous Article in Special Issue
Bacterial Substrate Transformation Tracked by Stable-Isotope-Guided NMR Metabolomics: Application in a Natural Aquatic Microbial Community
Open AccessArticle

Cell-Type Specific Metabolic Flux Analysis: A Challenge for Metabolic Phenotyping and a Potential Solution in Plants

Department of Plant Sciences, University of Oxford, Oxford OX1 3RB, UK
*
Authors to whom correspondence should be addressed.
Current address: The Francis Crick Institute, London NW1 1AT, UK.
Metabolites 2017, 7(4), 59; https://doi.org/10.3390/metabo7040059
Received: 27 September 2017 / Revised: 9 November 2017 / Accepted: 10 November 2017 / Published: 13 November 2017
(This article belongs to the Special Issue Isotope Guided Metabolomics and Flux Analysis)
Stable isotope labelling experiments are used routinely in metabolic flux analysis (MFA) to determine the metabolic phenotype of cells and tissues. A complication arises in multicellular systems because single cell measurements of transcriptomes, proteomes and metabolomes in multicellular organisms suggest that the metabolic phenotype will differ between cell types. In silico analysis of simulated metabolite isotopomer datasets shows that cellular heterogeneity confounds conventional MFA because labelling data averaged over multiple cell types does not necessarily yield averaged flux values. A potential solution to this problem—the use of cell-type specific reporter proteins as a source of cell-type specific labelling data—is proposed and the practicality of implementing this strategy in the roots of Arabidopsis thaliana seedlings is explored. A protocol for the immunopurification of ectopically expressed green fluorescent protein (GFP) from Arabidopsis thaliana seedlings using a GFP-binding nanobody is developed, and through GC-MS analysis of protein hydrolysates it is established that constitutively expressed GFP reports accurately on the labelling of total protein in root tissues. It is also demonstrated that the constitutive expression of GFP does not perturb metabolism. The principal obstacle to the implementation of the method in tissues with cell-type specific GFP expression is the sensitivity of the GC-MS system. View Full-Text
Keywords: Arabidopsis thaliana; cellular differentiation; green fluorescent protein (GFP); metabolic flux analysis; metabolic phenotype; primary metabolism; reporter protein; systems biology Arabidopsis thaliana; cellular differentiation; green fluorescent protein (GFP); metabolic flux analysis; metabolic phenotype; primary metabolism; reporter protein; systems biology
Show Figures

Figure 1

MDPI and ACS Style

Rossi, M.T.; Kalde, M.; Srisakvarakul, C.; Kruger, N.J.; Ratcliffe, R.G. Cell-Type Specific Metabolic Flux Analysis: A Challenge for Metabolic Phenotyping and a Potential Solution in Plants. Metabolites 2017, 7, 59.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Back to TopTop