The neuronal S100B protein is a calcium-tuned suppressor of amyloid-β aggregation - Science Advances
The neuronal S100B protein is a calcium-tuned suppressor of amyloid-β aggregation - Science Advances
The neuronal S100B protein is a calcium-tuned suppressor of amyloid-β aggregation Science Advances
We further speculated that the peak disappearances might also be caused either by the formation of a multimeric complex that is too large to be detected in the NMR experiments (although no precipitation was visible in the NMR titration experiments) or, ...
A persulfidation-based mechanism controls aquaporin-8 conductance - Science Advances
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A persulfidation-based mechanism controls aquaporin-8 conductance
Science Advances
1Protein Transport and Secretion Unit, Division of Genetics and Cell Biology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, UniversitÃ* Vita-Salute San Raffaele, 20132 Milan, Italy. 2Biomolecular Nuclear Magnetic ...
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A persulfidation-based mechanism controls aquaporin-8 conductance - Science Advances
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05-03-2018 06:46 PM
Protein Science by DNA Sequencing: How Advances in Molecular Biology Are Accelerating Biochemistry
Protein Science by DNA Sequencing: How Advances in Molecular Biology Are Accelerating Biochemistry
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.7b00886/20171020/images/medium/bi-2017-008868_0004.gif
Biochemistry
DOI: 10.1021/acs.biochem.7b00886
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10-24-2017 01:41 AM
[NMR paper] Distribution of amyloid-like and oligomeric species from protein aggregation kinetics
Distribution of amyloid-like and oligomeric species from protein aggregation kinetics
Amyloid fibrils and soluble oligomers are two types of protein aggregates associated with neurodegeneration. Classic therapeutic strategies try to prevent the nucleation and spread of amyloid fibrils, whilst diffusible oligomers have emerged as promising drug targets affecting downstream pathogenic processes. We developed a generic protein aggregation model and validate it against measured compositions of fibrillar and non-fibrillar assemblies of ataxin-3, a protein implicated in Machado-Joseph disease....
Recent advances in application of 27Al NMR spectroscopy to materials science
Recent advances in application of 27Al NMR spectroscopy to materials science
Publication date: May 2016
Source:Progress in Nuclear Magnetic Resonance Spectroscopy, Volumes 94–95</br>
Author(s): Mohamed Haouas, Francis Taulelle, Charlotte Martineau</br>
Valuable information about the local environment of the aluminum nucleus can be obtained through 27Al Nuclear Magnetic Resonance (NMR) parameters like the isotropic chemical shift, scalar and quadrupolar coupling constants, and relaxation rate. With nearly 250 scientific articles per year dealing with 27Al NMR...
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04-09-2016 03:54 AM
Solid-State NMR and FTIR Study of a Neuronal Calcium Sensor (NCS) Protein, Recoverin
Solid-State NMR and FTIR Study of a Neuronal Calcium Sensor (NCS) Protein, Recoverin
Publication date: 28 January 2014
Source:Biophysical Journal, Volume 106, Issue 2, Supplement 1</br>
Author(s): Kim Potvin-Fournier , Audrey Picard-Lafond , Melanie Schneider , Geneviève Valois-Paillard , Thierry Lefèvre , Philippe Calvez , Line Cantin , Christian Salesse , Michèle Auger</br>
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01-29-2014 12:50 AM
Structures Behind the Amyloid Aggregation of ?-Synuclein: An NMR Based Approach.
Structures Behind the Amyloid Aggregation of ?-Synuclein: An NMR Based Approach.
Structures Behind the Amyloid Aggregation of ?-Synuclein: An NMR Based Approach.
Curr Protein Pept Sci. 2011 Feb 24;
Authors: Orcellet ML, Fernández CO
The misfolding of proteins into a toxic conformation is proposed to be at the molecular foundation of a number of neurodegenerative disorders including Alzheimer's and Parkinson's diseases. Evidence that ?-synuclein amyloidogenesis plays a causative role in the development of Parkinson's disease is furnished by a...
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02-26-2011 11:56 AM
[NMR paper] Backbone dynamics of the calcium-signaling protein apo-S100B as determined by 15N NMR
Backbone dynamics of the calcium-signaling protein apo-S100B as determined by 15N NMR relaxation.
Related Articles Backbone dynamics of the calcium-signaling protein apo-S100B as determined by 15N NMR relaxation.
Biochemistry. 2001 Mar 27;40(12):3439-48
Authors: Inman KG, Baldisseri DM, Miller KE, Weber DJ
Backbone dynamics of homodimeric apo-S100B were studied by (15)N nuclear magnetic resonance relaxation at 9.4 and 14.1 T. Longitudinal relaxation (T(1)), transverse relaxation (T(2)), and the (15)N- NOE were measured for 80 of 91 backbone...