We describe an approach to efficiently determine the backbone conformation of solid proteins that utilizes selective and extensive (13)C labeling in conjunction with two-dimensional magic-angle-spinning NMR. The selective (13)C labeling approach aims to reduce line broadening and other multispin com
Two-compartment model for determination of glycolytic rates of solid tumors by in vivo13C NMR spectroscopy
β Scribed by Dmitri Artemov; Zaver M. Bhujwalla; Ulrich Pilatus; Jerry D. Glickson
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 125 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0952-3480
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β¦ Synopsis
Carbon-13 NMR spectroscopy of 13 C enriched substrates is useful for non-invasively determining metabolic fluxes of cells and tissues. Our study demonstrates that for RIF-1 tumor cells, examined under monolayer culture with continuous perfusion and also grown as solid subcutaneously (sc) implanted tumors in vivo, the levels of intracellular glucose and intermediates of the glycolytic pathway are below the level of detection by NMR spectroscopy. For these tumors, glucose transport into the cell is the most probable rate limiting step of the glycolytic pathway. Under these limiting conditions a simple two-compartment model of glycolysis applies. This model yields two parameters: the average rate of glycolysis and the rate of lactate clearance through the vasculature. For the RIF-1 tumor these parameters were 0.022 AE 0.01 and 0.034 AE 0.006 min Γ1 , respectively.
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A multiple-pulse technique for complete dipolar decoupling of ment, the directly detected dimension still exhibits 13 C-13 C directly bonded 13 C-labeled sites is described. It achieves signifidipolar splittings, which produce complex spectral patterns, cant spectral simplifications in a recently in
The orientations of the 13C chemical shift tensors in undoped cis-and tram-polyacetylene have been determined from the chemical shift-dipolar two-dimensional powder patterns observed in rotating samples.
## Abstract The complete assignment of cholesterol ^1^H and ^13^C NMR resonances in a lipid bilayer environment (L~Ξ±~βdimyristoylphosphatidylcholine/cholesterol 2:1) has been obtained by a combination of 1D and 2D MAS NMR experiments: ^13^C spectral editing, geβHSQC, dipolar HETCOR and Jβbased HETC