Mass Spectrometry as a Tool for Protein Crystallography
- 1 June 2001
- journal article
- review article
- Published by Annual Reviews in Annual Review of Biophysics
- Vol. 30 (1) , 67-85
- https://doi.org/10.1146/annurev.biophys.30.1.67
Abstract
Atomic resolution structure determinations of proteins by X-ray crystallography are formidable multidisciplinary undertakings, requiring protein construct design, expression and purification, crystallization trials, phase determination, and model building. Modern mass spectrometric methods can greatly facilitate these obligate tasks. Thus, mass spectrometry can be used to verify that the desired protein construct has been correctly expressed, to define compact domains in the target protein, to assess the components contained within the protein crystals, and to screen for successful incorporation of seleno-methionine and other heavy metal reagents used for phasing. In addition, mass spectrometry can be used to address issues of modeling, topology, and side-chain proximity. Here, we demonstrate how rational use of mass spectrometry assists and expedites high resolution X-ray structure determination through each stage of the process of protein crystallography.Keywords
This publication has 53 references indexed in Scilit:
- Four crystal structures of the 60 kDa flavoprotein monomer of the sulfite reductase indicate a disordered flavodoxin-like module 1 1Edited by R. HuberJournal of Molecular Biology, 2000
- Sequence-Specific RNA Binding by a Nova KH DomainCell, 2000
- Crystal structures of Nova-1 and Nova-2 K-homology RNA-binding domainsPublished by Elsevier ,1999
- Crystal Structure and Functional Analysis of the HERG Potassium Channel N Terminus: A Eukaryotic PAS DomainPublished by Elsevier ,1998
- The Structure of the Potassium Channel: Molecular Basis of K + Conduction and SelectivityScience, 1998
- Bioincorporation of telluromethionine into proteins: a promising new approach for X-ray structure analysis of proteinsJournal of Molecular Biology, 1997
- Domain Organization of theEscherichia coliRNA Polymerase σ70SubunitJournal of Molecular Biology, 1996
- Crystal structure of a TFIIB–TBP–TATA-element ternary complexNature, 1995
- Probing the solution structure of the DNA‐binding protein Max by a combination of proteolysis and mass spectrometryProtein Science, 1995
- Purification, characterization, crystallisation and X‐ray analysis of selenomethionine‐labelled hydroxymethylbilane synthase from Escherichia coliEuropean Journal of Biochemistry, 1993