Literature DB >> 12720277

Comparison of the three-dimensional structures of a human Bence-Jones dimer crystallized on Earth and aboard US Space Shuttle Mission STS-95.

Simon S Terzyan1, Christina R Bourne, Paul A Ramsland, Philip C Bourne, Allen B Edmundson.   

Abstract

Crystals of a human (Sea) Bence-Jones dimer were produced in a capillary by vapor diffusion under microgravity conditions in the 9 day US Space Shuttle Mission STS-95. In comparison to ground-based experiments, nucleation was facile and spontaneous in space. Appearance of a very large (8 x 1.6 x 1.0 mm) crystal in a short time period is a strong endorsement for the use of microgravity to produce crystals sufficiently large for neutron diffraction studies. The Sea dimer crystallized in the orthorhombic space group P2(1)2(1)2(1), with a = 48.9 A, b = 85.2 A, and c = 114.0 A. The crystals grown in microgravity exhibited significantly lower mosaicities than those of ground-based crystals and the X-ray diffraction data had a lower overall B factor. Three-dimensional structures determined by X-ray analysis at two temperatures (100 and 293 K) were indistinguishable from those obtained from ground-based crystals. However, both the crystallographic R factor and the free R factor were slightly lower in the models derived from crystals produced in microgravity. The major difference between the two crystal growth systems is a lack of convection and sedimentation in a microgravity environment. This environment resulted in the growth of much larger, higher-quality crystals of the Sea Bence-Jones protein. Structurally, heretofore unrecognized grooves on the external surfaces of the Sea and other immunoglobulin-derived fragments are regular features and may offer supplementary binding regions for super antigens and other elongated ligands in the bloodstream and perivascular tissues. Copyright 2003 John Wiley & Sons, Ltd.

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Year:  2003        PMID: 12720277     DOI: 10.1002/jmr.610

Source DB:  PubMed          Journal:  J Mol Recognit        ISSN: 0952-3499            Impact factor:   2.137


  3 in total

1.  Formation of amyloid fibers by monomeric light chain variable domains.

Authors:  Boris Brumshtein; Shannon R Esswein; Meytal Landau; Christopher M Ryan; Julian P Whitelegge; Martin L Phillips; Duilio Cascio; Michael R Sawaya; David S Eisenberg
Journal:  J Biol Chem       Date:  2014-08-19       Impact factor: 5.157

2.  Crystallographic analysis of ground and space thermostable T1 lipase crystal obtained via counter diffusion method approach.

Authors:  Sayangku Nor Ariati Mohamad Aris; Adam Leow Thean Chor; Mohd Shukuri Mohamad Ali; Mahiran Basri; Abu Bakar Salleh; Raja Noor Zaliha Raja Abd Rahman
Journal:  Biomed Res Int       Date:  2014-01-02       Impact factor: 3.411

3.  Inhibition by small-molecule ligands of formation of amyloid fibrils of an immunoglobulin light chain variable domain.

Authors:  Boris Brumshtein; Shannon R Esswein; Lukasz Salwinski; Martin L Phillips; Alan T Ly; Duilio Cascio; Michael R Sawaya; David S Eisenberg
Journal:  Elife       Date:  2015-11-18       Impact factor: 8.140

  3 in total

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