[NMR paper] Water proton NMR-a sensitive probe for solute association.
Water proton NMR-a sensitive probe for solute association.
Water proton NMR-a sensitive probe for solute association.
Chem Commun (Camb). 2015 Mar 19;
Authors: Feng Y, Taraban MB, Yu YB
Abstract
It is found that the transverse relaxation rate R2 of the water protons can be used to quantify protein aggregation and surfactant micellization in water. The simplicity and high intensity of the water proton signal enables non-invasive chemical analysis not readily achievable through solute proton signals, such as inspecting finished...
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[NMR paper] Fluorinated Aromatic Amino Acids are Sensitive 19F NMR Probes for Bromodomain-Ligand Interactions.
Fluorinated Aromatic Amino Acids are Sensitive 19F NMR Probes for Bromodomain-Ligand Interactions.
Related Articles Fluorinated Aromatic Amino Acids are Sensitive 19F NMR Probes for Bromodomain-Ligand Interactions.
ACS Chem Biol. 2014 Oct 7;
Authors: Mishra NK, Urick AK, Ember S, Schonbrunn E, Pomerantz WC
Abstract
We describe a 19F NMR method for detecting bromodomain-ligand interactions using fluorine-labeled aromatic amino acids due to the conservation of aromatic residues in the bromodomain binding site. We test the...
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10-08-2014 05:52 PM
A pH-Sensitive, Colorful,Lanthanide-Chelating ParamagneticNMR Probe
A pH-Sensitive, Colorful,Lanthanide-Chelating ParamagneticNMR Probe
Wei-Min Liu, Peter H. J. Keizers, Mathias A. S. Hass, Anneloes Blok, Monika Timmer, Alexi J. C. Sarris, Mark Overhand and Marcellus Ubbink
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja307824e/aop/images/medium/ja-2012-07824e_0011.gif
Journal of the American Chemical Society
DOI: 10.1021/ja307824e
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/NuKda-fEQQ4
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Site-Directed Methyl Group Labeling as an NMR Probe of Structure and Dynamics in Supramolecular Protein Systems: Applications to the Proteasome and to the ClpP Protease
Site-Directed Methyl Group Labeling as an NMR Probe of Structure and Dynamics in Supramolecular Protein Systems: Applications to the Proteasome and to the ClpP Protease
Tomasz L. Religa, Amy M. Ruschak, Rina Rosenzweig and Lewis E. Kay
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja202259a/aop/images/medium/ja-2011-02259a_0002.gif
Journal of the American Chemical Society
DOI: 10.1021/ja202259a
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/rQfCMlQFoW8
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Site-Directed Methyl Group Labeling as an NMR Probe of Structure and Dynamics in Supra-Molecular Protein Systems: Applications to the Proteasome and to the ClpP Protease.
Site-Directed Methyl Group Labeling as an NMR Probe of Structure and Dynamics in Supra-Molecular Protein Systems: Applications to the Proteasome and to the ClpP Protease.
Site-Directed Methyl Group Labeling as an NMR Probe of Structure and Dynamics in Supra-Molecular Protein Systems: Applications to the Proteasome and to the ClpP Protease.
J Am Chem Soc. 2011 May 11;
Authors: Religa TL, Ruschak AM, Rosenzweig R, Kay LE
Methyl groups are powerful reporters of structure, motion and function in NMR studies of supra-molecular protein assemblies. Their...
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[NMR paper] Using NMR as a probe of protein structure and function.
Using NMR as a probe of protein structure and function.
Related Articles Using NMR as a probe of protein structure and function.
Biochem Soc Trans. 1999 Aug;27(4):701-13
Authors: Malthouse JP