% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@INBOOK{Franke:453978,
author = {Franke, Daniel and Svergun, Dmitri I.},
title = {{S}ynchrotron {S}mall-{A}ngle {X}-{R}ay {S}cattering on
{B}iological {M}acromolecules in {S}olution},
address = {Cham},
publisher = {Springer International Publishing},
reportid = {PUBDB-2021-00335},
pages = {1645-1672},
year = {2020},
comment = {Synchrotron Light Sources and Free-Electron Lasers /
Jaeschke, Eberhard J. (Editor) ; Cham : Springer
International Publishing, 2020, Chapter 34 ; ISBN:
978-3-030-23200-9 ; doi:10.1007/978-3-030-23201-6},
booktitle = {Synchrotron Light Sources and
Free-Electron Lasers / Jaeschke,
Eberhard J. (Editor) ; Cham : Springer
International Publishing, 2020, Chapter
34 ; ISBN: 978-3-030-23200-9 ;
doi:10.1007/978-3-030-23201-6},
abstract = {Small-angle X-ray scattering (SAXS) is a powerful method
for the structural analysis of macromolecular solutions,
allowing one to study the structure of native particles and
complexes and to rapidly analyze structural changes in
response to variations in external conditions. On
synchrotrons, SAXS benefits enormously from the high
brilliance of the radiation, providing a considerable
advantage for the timescale of measurements (allowing also
for time-resolved experiments) and the small amounts of
material required. Emerging automation of the scattering
experiment, data processing, and interpretation make
synchrotron solution SAXS a streamline tool for large-scale
structural studies in molecular biology. In the present
chapter, a brief account will be given of the basic
principles of SAXS by macromolecular solutions and of the
synchrotron SAXS instrumentation. The main concepts of SAXS
data analysis from monodisperse solutions will be considered
and the methods for computation of the overall structural
parameters and ab initio low-resolution shape
reconstructions will be presented. Further, approaches
combining SAXS with other structural, biophysical, and
biochemical techniques including validation of predicted or
experimentally obtained high-resolution models in solution
and identification of biologically active oligomers will be
considered. Modeling methods of the quaternary structure of
macromolecular complexes in terms of rigid body
movements/rotations of individual subunits or domains will
be reviewed. The approaches will also be considered to study
oligomeric mixtures and to quantitatively characterize
flexible macromolecular systems, including intrinsically
unfolded proteins. The new methodological developments in
SAXS will be illustrated by examples of practical
applications.},
cin = {EMBL},
cid = {I:(DE-H253)EMBL-20120731},
pnm = {6G3 - PETRA III (POF3-622)},
pid = {G:(DE-HGF)POF3-6G3},
experiment = {EXP:(DE-H253)P-P12-20150101},
typ = {PUB:(DE-HGF)7},
doi = {10.1007/978-3-030-23201-6_34},
url = {https://bib-pubdb1.desy.de/record/453978},
}