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      Xlink Analyzer: Software for analysis and visualization of cross-linking data in the context of three-dimensional structures

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          Abstract

          Structural characterization of large multi-subunit protein complexes often requires integrating various experimental techniques. Cross-linking mass spectrometry (XL-MS) identifies proximal protein residues and thus is increasingly used to map protein interactions and determine the relative orientation of subunits within the structure of protein complexes. To fully adapt XL-MS as a structure characterization technique, we developed Xlink Analyzer, a software tool for visualization and analysis of XL-MS data in the context of the three-dimensional structures. Xlink Analyzer enables automatic visualization of cross-links, identifies cross-links violating spatial restraints, calculates violation statistics, maps chemically modified surfaces, and allows interactive manipulations that facilitate analysis of XL-MS data and aid designing new experiments. We demonstrate these features by mapping interaction sites within RNA polymerase I and the Rvb1/2 complex. Xlink Analyzer is implemented as a plugin to UCSF Chimera, a standard structural biology software tool, and thus enables seamless integration of XL-MS data with, e.g. fitting of X-ray structures to EM maps. Xlink Analyzer is available for download at http://www.beck.embl.de/XlinkAnalyzer.html.

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          Most cited references32

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          Matplotlib: A 2D Graphics Environment

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            Identification of cross-linked peptides from complex samples.

            We have developed pLink, software for data analysis of cross-linked proteins coupled with mass-spectrometry analysis. pLink reliably estimates false discovery rate in cross-link identification and is compatible with multiple homo- or hetero-bifunctional cross-linkers. We validated the program with proteins of known structures, and we further tested it on protein complexes, crude immunoprecipitates and whole-cell lysates. We show that it is a robust tool for protein-structure and protein-protein-interaction studies.
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              Molecular architecture of the 26S proteasome holocomplex determined by an integrative approach.

              The 26S proteasome is at the executive end of the ubiquitin-proteasome pathway for the controlled degradation of intracellular proteins. While the structure of its 20S core particle (CP) has been determined by X-ray crystallography, the structure of the 19S regulatory particle (RP), which recruits substrates, unfolds them, and translocates them to the CP for degradation, has remained elusive. Here, we describe the molecular architecture of the 26S holocomplex determined by an integrative approach based on data from cryoelectron microscopy, X-ray crystallography, residue-specific chemical cross-linking, and several proteomics techniques. The "lid" of the RP (consisting of Rpn3/5/6/7/8/9/11/12) is organized in a modular fashion. Rpn3/5/6/7/9/12 form a horseshoe-shaped heterohexamer, which connects to the CP and roofs the AAA-ATPase module, positioning the Rpn8/Rpn11 heterodimer close to its mouth. Rpn2 is rigid, supporting the lid, while Rpn1 is conformationally variable, positioned at the periphery of the ATPase ring. The ubiquitin receptors Rpn10 and Rpn13 are located in the distal part of the RP, indicating that they were recruited to the complex late in its evolution. The modular structure of the 26S proteasome provides insights into the sequence of events prior to the degradation of ubiquitylated substrates.
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                Author and article information

                Contributors
                Journal
                J Struct Biol
                J. Struct. Biol
                Journal of Structural Biology
                Academic Press
                1047-8477
                1095-8657
                1 March 2015
                March 2015
                : 189
                : 3
                : 177-183
                Affiliations
                European Molecular Biology Laboratory, Structural and Computational Biology Unit, Meyerhofstraße 1, 69117 Heidelberg, Germany
                Author notes
                [* ]Corresponding author. martin.beck@ 123456embl.de
                Article
                S1047-8477(15)00030-1
                10.1016/j.jsb.2015.01.014
                4359615
                25661704
                871f7819-ad0d-44d2-b98b-6077fac0abee
                © 2015 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 27 October 2014
                : 26 January 2015
                : 28 January 2015
                Categories
                Article

                Biophysics
                xl-ms, cross-linking mass spectrometry,ms, mass spectrometry,3d, three-dimensional,em, electron microscopy,pol i, rna polymerase i,ld-score, linear discriminant score,twh, tandem winged helix domain,cross-linking,mass spectrometry,visualization,analysis,xl-ms,integrative modeling

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