scholarly journals Amyloid β 42 fibril structure based on small-angle scattering

2021 ◽  
Vol 118 (48) ◽  
pp. e2112783118
Author(s):  
Veronica Lattanzi ◽  
Ingemar André ◽  
Urs Gasser ◽  
Marija Dubackic ◽  
Ulf Olsson ◽  
...  
Keyword(s):  
Cross Section ◽  
Small Angle ◽  
Small Angle Scattering ◽  
Scattering Data ◽  
Detailed Knowledge ◽  
Atomistic Model ◽  
Elliptical Cross ◽  
Fibril Structure ◽  
Angle Scattering ◽  
Starting State

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.

Interpretation of small-angle scattering data of inhomogeneous ellipsoids

2004 ◽  
Vol 37 (5) ◽  
pp. 815-822 ◽  
Author(s):  
Gerhard Fritz ◽  
Alexander Bergmann
Keyword(s):  
Cross Sections ◽  
Small Angle ◽  
Theoretical Calculations ◽  
Negative Contrast ◽  
Small Angle Scattering ◽  
Distribution Functions ◽  
Distance Distribution ◽  
Scattering Data ◽  
Elliptical Cross ◽  
Angle Scattering

Small-angle scattering data of inhomogeneous ellipsoidal particles are discussed in terms of their pair distance distribution functionsp(r). Special attention is given to the determination of core and shell thicknesses and axis ratios as well as to large distances within the particles, since cross terms between parts of positive and negative contrast within the particle can produce misleading results, similar to homogeneous particles or Janus particles. Cross-section pair distance distribution functionspc(r) of cylinders with elliptical cross sections show similar behaviour. Theoretical calculations are compared with small-angle X-ray and neutron scattering (SAXS and SANS) data of cetyltrimethylammonium bromide in aqueous KCl solutions.

Cross-Section Structure of Cylindrical and Polymer-like Micelles from Small-Angle Scattering Data. 2. Experimental Results

Langmuir ◽  
1996 ◽  
Vol 12 (10) ◽  
pp. 2433-2440 ◽  
Author(s):  
Peter Schurtenberger ◽  
Götz Jerke ◽  
Carolina Cavaco ◽  
Jan Skov Pedersen
Keyword(s):  
Cross Section ◽  
Small Angle ◽  
Small Angle Scattering ◽  
Experimental Results ◽  
Scattering Data ◽  
Angle Scattering ◽  
Section Structure

scholarly journals 2017 publication guidelines for structural modelling of small-angle scattering data from biomolecules in solution: an update

2017 ◽  
Vol 73 (9) ◽  
pp. 710-728 ◽  
Author(s):  
Jill Trewhella ◽  
Anthony P. Duff ◽  
Dominique Durand ◽  
Frank Gabel ◽  
J. Mitchell Guss ◽  
...  
Keyword(s):  
Small Angle ◽  
Task Force ◽  
Data Bank ◽  
Small Angle Scattering ◽  
Scattering Data ◽  
Quality Data ◽  
Angle Scattering ◽  
Publication Guidelines ◽  
Guidelines And Recommendations

In 2012, preliminary guidelines were published addressing sample quality, data acquisition and reduction, presentation of scattering data and validation, and modelling for biomolecular small-angle scattering (SAS) experiments. Biomolecular SAS has since continued to grow and authors have increasingly adopted the preliminary guidelines. In parallel, integrative/hybrid determination of biomolecular structures is a rapidly growing field that is expanding the scope of structural biology. For SAS to contribute maximally to this field, it is essential to ensure open access to the information required for evaluation of the quality of SAS samples and data, as well as the validity of SAS-based structural models. To this end, the preliminary guidelines for data presentation in a publication are reviewed and updated, and the deposition of data and associated models in a public archive is recommended. These guidelines and recommendations have been prepared in consultation with the members of the International Union of Crystallography (IUCr) Small-Angle Scattering and Journals Commissions, the Worldwide Protein Data Bank (wwPDB) Small-Angle Scattering Validation Task Force and additional experts in the field.

A Study of Beryllium-Based Materials and Comparison of Their X-Ray Homogeneities According to Small-Angle Scattering Data

2018 ◽  
Vol 63 (6) ◽  
pp. 874-882 ◽  
Author(s):  
A. A. Semenov ◽  
V. V. Volkov ◽  
A. V. Zabrodin ◽  
V. V. Gorlevskii ◽  
M. S. Sheverdyaev ◽  
...  
Keyword(s):  
Small Angle ◽  
Small Angle Scattering ◽  
Scattering Data ◽  
X Ray ◽  
Angle Scattering

scholarly journals Small-angle scattering data representation in SASCIF and integrative/hybrid methods dictionary

2017 ◽  
Vol 73 (a2) ◽  
pp. C1441-C1441
Author(s):  
Brinda Vallat ◽  
Benjamin Webb ◽  
John Westbrook ◽  
Andrej Sali ◽  
Helen Berman
Keyword(s):  
Small Angle ◽  
Hybrid Methods ◽  
Data Representation ◽  
Small Angle Scattering ◽  
Scattering Data ◽  
Angle Scattering

scholarly journals The canSAS standard for storing reduced one-dimensional small-angle scattering data in XML files

2008 ◽  
Vol 64 (a1) ◽  
pp. C554-C554
Author(s):  
P.R. Jemian ◽  
A.J. Jackson ◽  
S.M. King ◽  
K.C. Littrell ◽  
A.R.J. Nelson ◽  
...  
Keyword(s):  
Small Angle ◽  
Small Angle Scattering ◽  
Scattering Data ◽  
One Dimensional ◽  
Angle Scattering

Small-angle scattering of interacting particles. II. Generalized indirect Fourier transformation under consideration of the effective structure factor for polydisperse systems

1999 ◽  
Vol 32 (2) ◽  
pp. 197-209 ◽  
Author(s):  
B. Weyerich ◽  
J. Brunner-Popela ◽  
O. Glatter
Keyword(s):  
Form Factor ◽  
Small Angle ◽  
Structure Factor ◽  
Fourier Transformation ◽  
Hard Spheres ◽  
Small Angle Scattering ◽  
Scattering Data ◽  
Model Free ◽  
Angle Scattering ◽  
The Gift

The indirect Fourier transformation (IFT) is the method of choice for the model-free evaluation of small-angle scattering data. Unfortunately, this technique is only useful for dilute solutions because, for higher concentrations, particle interactions can no longer be neglected. Thus an advanced technique was developed as a generalized version, the so-called generalized indirect Fourier transformation (GIFT). It is based on the simultaneous determination of the form factor, representing the intraparticle contributions, and the structure factor, describing the interparticle contributions. The former can be determined absolutely free from model assumptions, whereas the latter has to be calculated according to an adequate model. In this paper, various models for the structure factor are compared,e.g.the effective structure factor for polydisperse hard spheres, the averaged structure factor, the local monodisperse approximation and the decoupling approximation. Furthermore, the structure factor for polydisperse rod-like particles is presented. As the model-free evaluation of small-angle scattering data is an essential point of the GIFT technique, the use of a structure factor without any influence of the form amplitude is advisable, at least during the first evaluation procedure. Therefore, a series of simulations are performed to check the possibility of the representation of various structure factors (such as the effective structure factor for hard spheres or the structure factor for rod-like particles) by the less exact but much simpler averaged structure factor. In all the observed cases, it was possible to recover the exact form factor with a free determined parameter set for the structure factor. The resulting parameters of the averaged structure factor have to be understood as apparent model parameters and therefore have only limited physical relevance. Thus the GIFT represents a technique for the model independent evaluation of scattering data with a minimum ofa prioriinformation.

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