small angle scattering
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2021 ◽  
Vol 12 (1) ◽  
pp. 90
Author(s):  
Sebastian Jaksch

Small-angle scattering, and its neutron expression small-angle neutron scattering (SANS), has developed into an invaluable tool for the investigation of microscopic and mesoscopic structures in recent decades [...]


BBA Advances ◽  
2021 ◽  
pp. 100033
Author(s):  
Kerrie A. Morrison ◽  
Aswin Doekhie ◽  
George M. Neville ◽  
Gareth J. Price ◽  
Paul Whitley ◽  
...  

2021 ◽  
Vol 242 (1) ◽  
Author(s):  
Sergey Zholudev ◽  
Tatiana Kiseleva ◽  
Aleksandr Chumakov ◽  
Eduard Levin ◽  
Vyacheslav Rusakov ◽  
...  

2021 ◽  
Vol 54 (6) ◽  
Author(s):  
Cedric J. Gommes ◽  
Sebastian Jaksch ◽  
Henrich Frielinghaus

Many experimental methods are available for the characterization of nanostructures, but most of them are limited by stringent experimental conditions. When it comes to analysing nanostructures in the bulk or in their natural environment – even as ordinary as water at room temperature – small-angle scattering (SAS) of X-rays or neutrons is often the only option. The rapid worldwide development of synchrotron and neutron facilities over recent decades has opened unprecedented possibilities for using SAS in situ and in a time-resolved way. But, in spite of its huge potential in the field of nanomaterials in general, SAS is covered far less than other characterization methods in non-specialized curricula. Presented here is a rigorous discussion of small-angle scattering, at a technical level comparable to the classical undergraduate coverage of X-ray diffraction by crystals and which contains diffraction as a particular case.


2021 ◽  
Vol 118 (48) ◽  
pp. e2112783118
Author(s):  
Veronica Lattanzi ◽  
Ingemar André ◽  
Urs Gasser ◽  
Marija Dubackic ◽  
Ulf Olsson ◽  
...  

Amyloid fibrils are associated with a number of neurodegenerative diseases, including fibrils of amyloid β42 peptide (Aβ42) in Alzheimer’s disease. These fibrils are a source of toxicity to neuronal cells through surface-catalyzed generation of toxic oligomers. Detailed knowledge of the fibril structure may thus facilitate therapeutic development. We use small-angle scattering to provide information on the fibril cross-section dimension and shape for Aβ42 fibrils prepared in aqueous phosphate buffer at pH = 7.4 and pH 8.0 under quiescent conditions at 37 °C from pure recombinant Aβ42 peptide. Fitting the data using a continuum model reveals an elliptical cross-section and a peptide mass-per-unit length compatible with two filaments of two monomers, four monomers per plane. To provide a more detailed atomistic model, the data were fitted using as a starting state a high-resolution structure of the two-monomer arrangement in filaments from solid-state NMR (Protein Data Bank ID 5kk3). First, a twofold symmetric model including residues 11 to 42 of two monomers in the filament was optimized in terms of twist angle and local packing using Rosetta. A two-filament model was then built and optimized through fitting to the scattering data allowing the two N-termini in each filament to take different conformations, with the same conformation in each of the two filaments. This provides an atomistic model of the fibril with twofold rotation symmetry around the fibril axis. Intriguingly, no polydispersity as regards the number of filaments was observed in our system over separate samples, suggesting that the two-filament arrangement represents a free energy minimum for the Aβ42 fibril.


2021 ◽  
Vol 54 (6) ◽  
Author(s):  
Jill Trewhella

Errors in the article by Jill Trewhella [J. Appl. Cryst. (2021), 54, 1029–1033] are corrected.


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