Structural characterization of proteins and complexes using small-angle X-ray solution scattering

被引:417
作者
Mertens, Haydyn D. T. [1 ]
Svergun, Dmitri I. [1 ]
机构
[1] European Mol Biol Lab, Hamburg Outstn, DESY, D-22603 Hamburg, Germany
关键词
Small-angle scattering; Solution scattering; Macromolecular structure; Functional complexes; Ab initio methods; Rigid body modeling; Flexible macromolecules; RESIDUAL DIPOLAR COUPLINGS; LOW-RESOLUTION; BIOLOGICAL MACROMOLECULES; SYNCHROTRON-RADIATION; NEUTRON-SCATTERING; ANALYTICAL ULTRACENTRIFUGATION; ASPARTATE TRANSCARBAMOYLASE; QUATERNARY STRUCTURE; SHAPE DETERMINATION; UNFOLDED PROTEINS;
D O I
10.1016/j.jsb.2010.06.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small-angle scattering of X-rays (SAXS) is an established method for the low-resolution structural characterization of biological macromolecules in solution. The technique provides three-dimensional low-resolution structures, using ab initio and rigid body modeling, and allow one to assess the oligomeric state of proteins and protein complexes. In addition, SAXS is a powerful tool for structure validation and the quantitative analysis of flexible systems, and is highly complementary to the high resolution methods of X-ray crystallography and NMR. At present, SAXS analysis methods have reached an advanced state, allowing for automated and rapid characterization of protein solutions in terms of low-resolution models, quaternary structure and oligomeric composition. In this communication, main approaches to the characterization of proteins and protein complexes using SAXS are reviewed. The tools for the analysis of proteins in solution are presented, and the impact that these tools have made in modern structural biology is discussed. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:128 / 141
页数:14
相关论文
共 101 条
[1]  
[Anonymous], 1987, Structure Analysis by Small-Angle X-Ray and Neutron Scattering
[2]  
[Anonymous], 1982, Small angle x-ray scattering, DOI DOI 10.1002/ACTP.1985.010360520
[3]   Folded-back solution structure of monomeric factor H of human complement by synchrotron X-ray and neutron scattering, analytical ultracentrifugation and constrained molecular modelling [J].
Aslam, M ;
Perkins, SJ .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 309 (05) :1117-1138
[4]   Solution structural studies and low-resolution model of the Schizosaccharomyces pombe sap1 protein [J].
Bada, M ;
Walther, D ;
Arcangioli, B ;
Doniach, S ;
Delarue, M .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (03) :563-574
[5]   SoftWAXS: a computational tool for modeling wide-angle X-ray solution scattering from biomolecules [J].
Bardhan, Jaydeep ;
Park, Sanghyun ;
Makowski, Lee .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2009, 42 :932-943
[6]   Dipolar couplings in macromolecular structure determination [J].
Bax, A ;
Kontaxis, G ;
Tjandra, N .
NUCLEAR MAGNETIC RESONANCE OF BIOLOGICAL MACROMOLECULES, PT B, 2001, 339 :127-174
[7]   A structural model for unfolded proteins from residual dipolar couplings and small-angle x-ray scattering [J].
Bernadó, P ;
Blanchard, L ;
Timmins, P ;
Marion, D ;
Ruigrok, RWH ;
Blackledge, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (47) :17002-17007
[8]  
BERNADO P, 2009, EUR BIOPHYS J 1021
[9]   Structural characterization of flexible proteins using small-angle X-ray scattering [J].
Bernado, Pau ;
Mylonas, Efstratios ;
Petoukhov, Maxim V. ;
Blackledge, Martin ;
Svergun, Dmitri I. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (17) :5656-5664
[10]   The Fab and Fc fragments of IgA1 exhibit a different arrangement from that in IgG: A study by X-ray and neutron solution scattering and homology modelling [J].
Boehm, MK ;
Woof, JM ;
Kerr, MA ;
Perkins, SJ .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 286 (05) :1421-1447