Related ArticlesHeteronuclear NMR As a 4-in-1 Analytical Platform for Detecting Modification-Specific Signatures of Therapeutic Insulin Formulations.
Anal Chem. 2014 Feb 5;
Authors: Jin X, Kang S, Kwon H, Park S
Abstract
Detecting possible modifications of therapeutic proteins is a critical element of the quality control of protein drugs. Typically, a number of techniques are used to evaluate different modifications of therapeutic protein formulations. Using heteronuclear NMR spectroscopy, we show that the difference between various insulin formulations can be detected "as is" with little pretreatment and quickly. As an application to the quality control of insulin formulations, the NMR approach was compared with four different analytical methods: with reverse phase high pressure liquid chromatography (HPLC) (for mutations), with size exclusion chromatography (for oligomerization), with electrophoresis (for denaturation), and with mass spectrometry (for deamidation). All of the results showed that this single NMR method can provide the specific signatures for each modification and information that is at least equivalent to that offered by the conventional analytical methods. Importantly, NMR could yield information at each amino acid residue level which no other technique provided. The suggested NMR method, then, can be considered to be a facile and effective means of evaluating therapeutic protein formulations in a multifaceted way.
PMID: 24499031 [PubMed - as supplied by publisher]
DynamicNuclear Polarization Enhanced NMR Spectroscopyfor Pharmaceutical Formulations
DynamicNuclear Polarization Enhanced NMR Spectroscopyfor Pharmaceutical Formulations
Aaron J. Rossini, Cory M. Widdifield, Alexandre Zagdoun, Moreno Lelli, Martin Schwarzwa?lder, Christophe Cope?ret, Anne Lesage and Lyndon Emsley
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja4092038/aop/images/medium/ja-2013-092038_0008.gif
Journal of the American Chemical Society
DOI: 10.1021/ja4092038
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/nHKQlpO4cTw
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[NMR paper] Heteronuclear NMR provides an accurate assessment of therapeutic insulin's quality.
Heteronuclear NMR provides an accurate assessment of therapeutic insulin's quality.
Related Articles Heteronuclear NMR provides an accurate assessment of therapeutic insulin's quality.
J Pharm Biomed Anal. 2013 Feb 20;78-79C:252-254
Authors: Quinternet M, Starck JP, Delsuc MA, Kieffer B
Abstract
New generations of drugs are using more and more often therapeutic proteins as the active ingredient, prompting the regulation agencies to adapt their analytical methods. Fast and unambiguous information on the secondary, tertiary and quaternary...
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03-19-2013 01:22 PM
[NMR paper] Heteronuclear NMR studies of the specificity of the post-translational modification o
Heteronuclear NMR studies of the specificity of the post-translational modification of biotinyl domains by biotinyl protein ligase.
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FEBS Lett. 2000 Aug 18;479(3):93-8
Authors: Reche PA, Howard MJ, Broadhurst RW, Perham RN
The lipoyl domains of 2-oxo acid dehydrogenase multienzyme complexes and the biotinyl domains of biotin-dependent enzymes have homologous structures, but the target lysine...
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[NMR paper] Probing site-specific interactions in protein-DNA complexes using heteronuclear NMR s
Probing site-specific interactions in protein-DNA complexes using heteronuclear NMR spectroscopy and molecular modeling: binding of Cro repressor to OR3.
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J Biomol Struct Dyn. 1998 Aug;16(1):13-20
Authors: Edwards CA, Tung CS, Silks LA, Gatewood JM, Fee JA, Mariappan SV
In this paper, a general method is developed to study site-specific interactions in DNA-protein complexes...
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[NMR paper] Comparative 2D NMR studies of human insulin and des-pentapeptide insulin: sequential
Comparative 2D NMR studies of human insulin and des-pentapeptide insulin: sequential resonance assignment and implications for protein dynamics and receptor recognition.
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Biochemistry. 1991 Jun 4;30(22):5505-15
Authors: Hua QX, Weiss MA
The solution structure and dynamics of human insulin are investigated by 2D 1H NMR spectroscopy in reference to a previously...
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[NMR paper] Heteronuclear 2D NMR studies of an engineered insulin monomer: assignment and charact
Heteronuclear 2D NMR studies of an engineered insulin monomer: assignment and characterization of the receptor-binding surface by selective 2H and 13C labeling with application to protein design.
Related Articles Heteronuclear 2D NMR studies of an engineered insulin monomer: assignment and characterization of the receptor-binding surface by selective 2H and 13C labeling with application to protein design.
Biochemistry. 1991 Jul 30;30(30):7373-89
Authors: Weiss MA, Hua QX, Lynch CS, Frank BH, Shoelson SE
Insulin provides an important model for...
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08-21-2010 11:12 PM
[NMR paper] Heteronuclear 2D NMR studies of an engineered insulin monomer: assignment and charact
Heteronuclear 2D NMR studies of an engineered insulin monomer: assignment and characterization of the receptor-binding surface by selective 2H and 13C labeling with application to protein design.
Related Articles Heteronuclear 2D NMR studies of an engineered insulin monomer: assignment and characterization of the receptor-binding surface by selective 2H and 13C labeling with application to protein design.
Biochemistry. 1991 Jul 30;30(30):7373-89
Authors: Weiss MA, Hua QX, Lynch CS, Frank BH, Shoelson SE
Insulin provides an important model for...
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[NMR paper] Complete sequence-specific 1H NMR assignments for human insulin.
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Biochemistry. 1990 Mar 27;29(12):2906-13
Authors: Kline AD, Justice RM
Solvent conditions where human insulin could be studied by high-resolution NMR were determined. Both low pH and addition of acetonitrile were required to overcome the protein's self-association and to obtain useful spectra. Two hundred eighty-six 1H resonances were located and assigned to specific sites on the protein by using...