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1.
Acta Crystallogr D Biol Crystallogr ; 62(Pt 10): 1137-49, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17001091

ABSTRACT

This paper reviews the developments in high-throughput and nanolitre-scale protein crystallography technologies within the remit of workpackage 4 of the Structural Proteomics In Europe (SPINE) project since the project's inception in October 2002. By surveying the uptake, use and experience of new technologies by SPINE partners across Europe, a picture emerges of highly successful adoption of novel working methods revolutionizing this area of structural biology. Finally, a forward view is taken of how crystallization methodologies may develop in the future.


Subject(s)
Crystallography/methods , Proteins/chemistry , Crystallography/instrumentation , Crystallography/trends , Image Processing, Computer-Assisted , Nanotechnology , Plastics , Proteomics , Quality Control , Robotics
2.
Proc Natl Acad Sci U S A ; 102(1): 57-62, 2005 Jan 04.
Article in English | MEDLINE | ID: mdl-15618400

ABSTRACT

Protein-protein interactions are essential for life. Yet, our understanding of the general principles governing binding is not complete. In the present study, we show that the interface between proteins is built in a modular fashion; each module is comprised of a number of closely interacting residues, with few interactions between the modules. The boundaries between modules are defined by clustering the contact map of the interface. We show that mutations in one module do not affect residues located in a neighboring module. As a result, the structural and energetic consequences of the deletion of entire modules are surprisingly small. To the contrary, within their module, mutations cause complex energetic and structural consequences. Experimentally, this phenomenon is shown on the interaction between TEM1-beta-lactamase and beta-lactamase inhibitor protein (BLIP) by using multiple-mutant analysis and x-ray crystallography. Replacing an entire module of five interface residues with Ala created a large cavity in the interface, with no effect on the detailed structure of the remaining interface. The modular architecture of binding sites, which resembles human engineering design, greatly simplifies the design of new protein interactions and provides a feasible view of how these interactions evolved.


Subject(s)
Models, Molecular , Proteins/chemistry , Proteins/metabolism , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Binding Sites/genetics , Binding Sites/physiology , Mutation , Protein Binding , Protein Structure, Tertiary , Proteins/genetics , Thermodynamics , beta-Lactamases/chemistry , beta-Lactamases/genetics , beta-Lactamases/metabolism
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