[ASAP] Constraints on the Structure of Fibrils Formed by a Racemic Mixture of Amyloid-? Peptides from Solid-State NMR, Electron Microscopy, and Theory
Constraints on the Structure of Fibrils Formed by a Racemic Mixture of Amyloid-? Peptides from Solid-State NMR, Electron Microscopy, and Theory
Jevgenij A. Raskatov, Alejandro R. Foley, John M. Louis, Wai-Ming Yau, and Robert Tycko
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.1c06339/20210810/images/medium/ja1c06339_0009.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.1c06339
http://feeds.feedburner.com/~r/acs/jacsat/~4/icEctWA9HQc
[ASAP] Tailorable Indirect to Direct Band-Gap Double Perovskites with Bright White-Light Emission: Decoding Chemical Structure Using Solid-State NMR
Tailorable Indirect to Direct Band-Gap Double Perovskites with Bright White-Light Emission: Decoding Chemical Structure Using Solid-State NMR
Abhoy Karmakar†, Guy M. Bernard†, Alkiviathes Meldrum‡, Anton O. Oliynyk§, and Vladimir K. Michaelis*†
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.0c02198/20200604/images/medium/ja0c02198_0010.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.0c02198
http://feeds.feedburner.com/~r/acs/jacsat/~4/0mALpvaVuq4
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[NMR paper] 3D Structure Determination of Amyloid Fibrils using Solid-State NMR Spectroscopy.
3D Structure Determination of Amyloid Fibrils using Solid-State NMR Spectroscopy.
3D Structure Determination of Amyloid Fibrils using Solid-State NMR Spectroscopy.
Methods. 2018 Apr 05;:
Authors: Loquet A, El Mammeri N, Stanek J, Berbon M, Bardiaux B, Pintacuda G, Habenstein B
Abstract
The amyloid fold is structurally characterized by a typical cross-? architecture, which is under debate to represent an energy-favourable folding state that many globular or natively unfolded proteins can adopt. Being initially solely associated...
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04-09-2018 11:12 AM
[NMR paper] The effect of drug binding on specific sites in transmembrane helices 4 and 6 of the ABC exporter MsbA studied by DNP-enhanced solid-state NMR.
The effect of drug binding on specific sites in transmembrane helices 4 and 6 of the ABC exporter MsbA studied by DNP-enhanced solid-state NMR.
Related Articles The effect of drug binding on specific sites in transmembrane helices 4 and 6 of the ABC exporter MsbA studied by DNP-enhanced solid-state NMR.
Biochim Biophys Acta. 2017 Oct 22;:
Authors: Spadaccini R, Kaur H, Becker-Baldus J, Glaubitz C
Abstract
MsbA, a homodimeric ABC exporter, translocates its native substrate lipid A as well as a range of smaller, amphiphilic...
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10-28-2017 08:03 AM
Solid-state NMR analysis of interaction sites of curcumin and 42-residue amyloid ?-protein fibrils.
Solid-state NMR analysis of interaction sites of curcumin and 42-residue amyloid ?-protein fibrils.
Solid-state NMR analysis of interaction sites of curcumin and 42-residue amyloid ?-protein fibrils.
Bioorg Med Chem. 2011 Aug 27;
Authors: Masuda Y, Fukuchi M, Yatagawa T, Tada M, Takeda K, Irie K, Akagi KI, Monobe Y, Imazawa T, Takegoshi K
Abstract
Aggregation of 42-residue amyloid ?-protein (A?42) plays a pivotal role in the etiology of Alzheimer's disease (AD). Curcumin, the yellow pigment in the rhizome of turmeric, attracts...
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09-20-2011 03:10 PM
Molecular-Level Examination of Cu2+ Binding Structure for Amyloid Fibrils of 40-Residue Alzheimer’s ? by Solid-State NMR Spectroscopy
Molecular-Level Examination of Cu2+ Binding Structure for Amyloid Fibrils of 40-Residue Alzheimer’s ? by Solid-State NMR Spectroscopy
Sudhakar Parthasarathy, Fei Long, Yifat Miller, Yiling Xiao, Dan McElheny, Kent Thurber, Buyong Ma, Ruth Nussinov and Yoshitaka Ishii
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja1072178/aop/images/medium/ja-2010-072178_0006.gif
Journal of the American Chemical Society
DOI: 10.1021/ja1072178
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA ...
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02-22-2011 11:06 PM
Probing water-accessibility in HET-s(218-289) amyloid fibrils by solid-state NMR.
Probing water-accessibility in HET-s(218-289) amyloid fibrils by solid-state NMR.
Probing water-accessibility in HET-s(218-289) amyloid fibrils by solid-state NMR.
J Mol Biol. 2010 Nov 18;
Authors: Van Melckebeke H, Schanda P, Gath J, Wasmer C, Verel R, Lange A, Meier BH, Böckmann A
Despite its importance in the context of conformational diseases, structural information is still sparse for protein fibrils. Hydrogen/deuterium exchange measurements of backbone amides allow to identify hydrogen-bonding patterns and reveal pertinent information about...