Quantitative Detection of Pegylated Biomacromolecules in Biological Fluids by NMR.
Anal Chem. 2016 Feb 29;
Authors: Alvares RD, Hasabnis A, Prosser RS, Macdonald PM
Abstract
The accumulation, bio-distribution and clearance profiles of therapeutic agents are key factors relevant to their efficacy. Determining these properties constitutes an ongoing experimental challenge. Many such therapeutics, including small molecules, peptides, proteins, tissue scaffolds, and drug delivery vehicles, are conjugated to poly(ethylene glycol) (PEG) as this improves their bioavailability and in vivo stability. We demonstrate here that 1H nuclear magnetic resonance (NMR) spectroscopy can be used to quantify PEGylated species in complex biological fluids directly, rapidly and with minimal sample preparation. PEG bears a large number of spectroscopically equivalent protons exhibiting a narrow NMR line width while resonating at a 1H NMR frequency distinct from most other biochemical signals. We demonstrate that PEG provides a robust signal allowing detection of concentrations as low as 10 µg/mL in blood. This PEG detection limit is lowered by another order of magnitude when background proton signals are minimized using 13C-enriched PEG in combination with a double quantum filter to remove (1)H signals from non-13C-labelled species. Quantitative detection of PEG via these methods is shown in pig blood and goat serum as examples of complex biological fluids. More practically, we quantify the blood clearance of (13)C-PEG and PEGylated-BSA (bovine serum albumin) following their intravenous injection in live rats. Given the relative insensitivity of line width to PEG size, we anticipate that the biodistribution and clearance profiles of virtually any PEGylated biomacromolecule from biological fluid samples can be routinely measured by 1H NMR without any filtering or treatment steps.
PMID: 26927487 [PubMed - as supplied by publisher]
[NMR paper] Solid-State NMR of PEGylated Proteins.
Solid-State NMR of PEGylated Proteins.
Related Articles Solid-State NMR of PEGylated Proteins.
Angew Chem Int Ed Engl. 2016 Jan 12;
Authors: Ravera E, Ciambellotti S, Cerofolini L, Martelli T, Kozyreva T, Bernacchioni C, Giuntini S, Fragai M, Turano P, Luchinat C
Abstract
PEGylated proteins are widely used in biomedicine but, in spite of their importance, no atomic-level information is available since they are generally resistant to structural characterization approaches. PEGylated proteins are shown here to yield highly resolved...
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01-13-2016 05:24 PM
Study of PEGylated model protein reveals porous structure based on PEG size - Phys.Org
Study of PEGylated model protein reveals porous structure based on PEG size - Phys.Org
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Study of PEGylated model protein reveals porous structure based on PEG size
Phys.Org
NMR studies using 1H-15N heteronuclear single-quantum correlation spectroscopy showed that the PEG-Pc had well-dispersed resonances that indicated the protein remained folded in a stable conformation. Chemical shift perturbations were only...
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09-22-2015 06:40 PM
[NMR paper] In-Cell NMR and EPR Spectroscopy of Biomacromolecules.
In-Cell NMR and EPR Spectroscopy of Biomacromolecules.
In-Cell NMR and EPR Spectroscopy of Biomacromolecules.
Angew Chem Int Ed Engl. 2014 Jul 28;
Authors: Hänsel R, Luh LM, Corbeski I, Trantirek L, Dötsch V
Abstract
The dream of cell biologists is to be able to watch biological macromolecules perform their duties in the intracellular environment of live cells. Ideally, the observation of both the location and the conformation of these macromolecules with biophysical techniques is desired. The development of many fluorescence...
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07-30-2014 10:22 AM
[NMR paper] NMR Spectroscopy on Domain Dynamics in Biomacromolecules.
NMR Spectroscopy on Domain Dynamics in Biomacromolecules.
Related Articles NMR Spectroscopy on Domain Dynamics in Biomacromolecules.
Prog Biophys Mol Biol. 2013 May 15;
Authors: Shapiro YE
Abstract
Domain dynamics in biomacromolecules is currently an area of intense research because of its importance for understanding the huge quantity of available data relating the structure and function of proteins and nucleic acids. Control of structural flexibility is essential for the proper functioning of the biomacromolecules. Biophysical...
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05-21-2013 02:34 PM
Journal Highlight: Quantitative NMR: An applicable method for quantitative analysis of medicinal plant extracts and herbal products
Journal Highlight: Quantitative NMR: An applicable method for quantitative analysis of medicinal plant extracts and herbal products
http://www.spectroscopynow.com/common/images/thumbnails/13abcca009b.jpgA quantitative NMR method has been reported for quantitative analysis of three medicinal plant extracts and their herbal products without the need of authentic standards.
Source: Spectroscopynow.com
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02-03-2013 08:49 AM
Ultrafast quantitative 2D NMR: an efficient tool for the measurement of specific isotopic enrichments in complex biological mixtures.
Ultrafast quantitative 2D NMR: an efficient tool for the measurement of specific isotopic enrichments in complex biological mixtures.
Ultrafast quantitative 2D NMR: an efficient tool for the measurement of specific isotopic enrichments in complex biological mixtures.
Anal Chem. 2011 Apr 15;83(8):3112-9
Authors: Giraudeau P, Massou S, Robin Y, Cahoreau E, Portais JC, Akoka S
Two-dimensional nuclear magnetic resonance (2D NMR) is a promising tool for studying metabolic fluxes by measuring (13)C-enrichments in complex mixtures of (13)C-labeled...
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08-04-2011 11:41 AM
[NMR paper] Lipid-protein stoichiometries in a crystalline biological membrane: NMR quantitative
Lipid-protein stoichiometries in a crystalline biological membrane: NMR quantitative analysis of the lipid extract of the purple membrane.
Related Articles Lipid-protein stoichiometries in a crystalline biological membrane: NMR quantitative analysis of the lipid extract of the purple membrane.
J Lipid Res. 2002 Jan;43(1):132-40
Authors: Corcelli A, Lattanzio VM, Mascolo G, Papadia P, Fanizzi F
The lipid/protein stoichiometries of a naturally crystalline biological membrane, the purple membrane (PM) of Halobacterium salinarum, have been...
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11-24-2010 08:49 PM
[NMR paper] Analysis of biological fluids using 600 MHz proton NMR spectroscopy: application of h
Analysis of biological fluids using 600 MHz proton NMR spectroscopy: application of homonuclear two-dimensional J-resolved spectroscopy to urine and blood plasma for spectral simplification and assignment.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles Analysis of biological fluids using 600 MHz proton NMR spectroscopy: application of homonuclear two-dimensional J-resolved spectroscopy to urine and blood plasma for spectral simplification and assignment.
J Pharm Biomed Anal. 1993...