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Cover illustration: ICCBM10 |
Acta Cryst. (2005). D61, 651-657 [ doi:10.1107/S0907444905007808 ] A procedure for setting up high-throughput nanolitre crystallization experiments. Crystallization workflow for initial screening, automated storage, imaging and optimizationT. S. Walter, J. M. Diprose, C. J. Mayo, C. Siebold, M. G. Pickford, L. Carter, G. C. Sutton, N. S. Berrow, J. Brown, I. M. Berry, G. B. E. Stewart-Jones, J. M. Grimes, D. K. Stammers, R. M. Esnouf, E. Y. Jones, R. J. Owens, D. I. Stuart and K. HarlosSynopsis: The current workflow for crystallization at the Oxford Protein Production Facility (OPPF) is described. Online 26 May 2005 |
Acta Cryst. (2005). D61, 658-663 [ doi:10.1107/S090744490500939X ] Development of a fully automated macromolecular crystallization/observation robotic system, HTS-80H. Miyatake, S.-H. Kim, I. Motegi, H. Matsuzaki, H. Kitahara, A. Higuchi and K. MikiSynopsis: A fully automated robotic system for the crystallization and observation of macromolecules, HTS-80, has been developed. Online 26 May 2005 |
Acta Cryst. (2005). D61, 664-670 [ doi:10.1107/S0907444905000028 ] High-throughput crystal-optimization strategies in the South Paris Yeast Structural Genomics Project: one size fits all?N. Leulliot, L. Trésaugues, M. Bremang, I. Sorel, N. Ulryck, M. Graille, I. Aboulfath, A. Poupon, D. Liger, S. Quevillon-Cheruel, J. Janin and H. van TilbeurghSynopsis: Discussion of high-throughput optimization strategies used in the Yeast Structural Genomics Project, with selected successful examples. Online 26 May 2005 |
Acta Cryst. (2005). D61, 671-678 [ doi:10.1107/S0907444905001290 ] HalX: an open-source LIMS (Laboratory Information Management System) for small- to large-scale laboratoriesJ. Prilusky, E. Oueillet, N. Ulryck, A. Pajon, J. Bernauer, I. Krimm, S. Quevillon-Cheruel, N. Leulliot, M. Graille, D. Liger, L. Trésaugues, J. L. Sussman, J. Janin, H. van Tilbeurgh and A. PouponSynopsis: HalX, software designed as an `electronic lab book', aims at (i) storage and (ii) easy access and use of all experimental data. Its use should lead to much improved management and tracking of structural genomics experimental data. Online 26 May 2005 |
Acta Cryst. (2005). D61, 679-684 [ doi:10.1107/S0907444905013132 ] The high-throughput protein-to-structure pipeline at SECSGZ.-J. Liu, W. Tempel, J. D. Ng, D. Lin, A. K. Shah, L. Chen, P. S. Horanyi, J. E. Habel, I. A. Kataeva, H. Xu, H. Yang, J. C. Chang, L. Huang, S.-H. Chang, W. Zhou, D. Lee, J. L. Praissman, H. Zhang, M. G. Newton, J. P. Rose, J. S. Richardson, D. C. Richardson and B.-C. WangSynopsis: The high-throughput crystal structure determination pipeline at Southeast Collaboratory for Structural Genomics, a pilot center of the National Institutes of Health Protein Structure Initiative, is described. Online 26 May 2005 |
Acta Cryst. (2005). D61, 685-689 [ doi:10.1107/S0907444904028707 ] Crystallization and crystal manipulation of the Pterocarpus angolensis seed lectinR. Loris, A. Garcia-Pino, L. Buts, J. Bouckaert, S. Beeckmans, H. De Greve and L. WynsSynopsis: The Man/Glc-specific lectin from P. angolensis was crystallized in complex with Man( Online 26 May 2005 |
Acta Cryst. (2005). D61, 690-693 [ doi:10.1107/S0907444904029348 ] Crystallization and preliminary X-ray analysis of strictosidine synthase and its complex with the substrate tryptamineJ. Koepke, X. Ma, G. Fritzsch, H. Michel and J. StöckigtSynopsis: Strictosidine synthase is a central enzyme that participates in the biosynthesis of plant monoterpenoid indole alkaloids. The native enzyme and its complex with the substrate tryptamine were crystallized and analyzed by X-rays. Online 26 May 2005 |
Acta Cryst. (2005). D61, 694-696 [ doi:10.1107/S0907444904028756 ] Crystallization and preliminary X-ray analysis of native and selenomethionyl vinorine synthase from Rauvolfia serpentinaX. Ma, J. Koepke, A. Bayer, G. Fritzsch, H. Michel and J. StöckigtSynopsis: Crystals of vinorine synthase and selenomethionyl-labelled vinorine synthase have been obtained by a hanging-drop method and were analyzed by X-ray crystallography. Vinorine synthase is the first crystallized enzyme which belongs to the BAHD superfamily. Online 26 May 2005 |
Acta Cryst. (2005). D61, 697-700 [ doi:10.1107/S0907444905014174 ] Crystallization of soluble urokinase receptor (suPAR) in complex with urokinase amino-terminal fragment (1-143)M. Huang, A. P. Mazar, G. Parry, A.A.-R. Higazi, A. Kuo and D. B. CinesSynopsis: Crystallization of a suPAR-ATF complex. Online 26 May 2005 |
Acta Cryst. (2005). D61, 704-709 [ doi:10.1107/S0907444905006761 ] Crystallization of canavalin as a function of pHE. L. Forsythe, S. Gorti and M. L. PuseySynopsis: Canavalin is found to crystallize from pH 6.4 to 9.6. Fluorescence anisotropy and light-scattering measurements indicate that the solution is composed of trimers. Online 26 May 2005 |
Acta Cryst. (2005). D61, 710-712 [ doi:10.1107/S0907444905006864 ] Preliminary X-ray crystallographic analysis of thermolysin in the presence of 4 M NaClM. Kamo, K. Inouye, K. Nagata and M. TanokuraSynopsis: This report details a new method to introduce high concentrations of NaCl into crystals of thermolysin. The crystal obtained by this method diffracted X-rays to 2.43 Å and the crystal structure of thermolysin in the presence of 4 M NaCl was solved for the first time. Online 26 May 2005 |
Acta Cryst. (2005). D61, 713-719 [ doi:10.1107/S0907444905006311 ] Reproducible growth of well diffracting ribosomal crystalsT. Auerbach-Nevo, R. Zarivach, M. Peretz and A. YonathSynopsis: The crystal quality of the large ribosomal subunit was enhanced using active-state ribosomes. Online 26 May 2005 |
Acta Cryst. (2005). D61, 720-723 [ doi:10.1107/S0907444904030756 ] The incorporation of large impurities into virus crystalsYu. G. Kuznetsov, D. L. Makino, A. J. Malkin and A. McPhersonSynopsis: Virus crystals can incorporate a wide range of unusual impurities, not possible for conventional crystals or even most protein crystals, because of the large size of their constituent particles. Examples of several of these unusual impurities are presented here, along with some of the consequences for the crystal lattices. Online 26 May 2005 |
Acta Cryst. (2005). D61, 724-730 [ doi:10.1107/S0907444904029063 ] The role of protein and surfactant interactions in membrane-protein crystallizationB. W. Berger, C. M. Gendron, C. R. Robinson, E. W. Kaler and A. M. LenhoffSynopsis: Interactions leading to crystallization of the integral membrane protein bacteriorhodopsin were investigated. Osmotic second virial coefficients were measured by self-interaction chromatography. Online 26 May 2005 |
Acta Cryst. (2005). D61, 731-736 [ doi:10.1107/S0907444905009595 ] Structure determination of GGA-GAE and
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Acta Cryst. (2005). D61, 737-743 [ doi:10.1107/S0907444905000053 ] The mechanism of high-pressure-induced ordering in a macromolecular crystalT. Lin, W. Schildkamp, K. Brister, P. C. Doerschuk, M. Somayazulu, H. Mao and J. E. JohnsonSynopsis: A mechanistic model consistent with experimental data is proposed for the pressure-induced ordering of a macromolecular crystal. Online 26 May 2005 |
Acta Cryst. (2005). D61, 744-749 [ doi:10.1107/S0907444905006724 ] Different crystal packing in Fab-protein L semi-disordered peptide complexR. Ménez, N. G. Housden, S. Harrison, C. Jolivet-Reynaud, M. G. Gore and E. A. SturaSynopsis: Peptides whose conformation is ill defined can be crystallized in complex with proteins where in the lattice they will adopt multiple conformations. The peptide in complex with an anti-HCV monoclonal antibody is most ordered where it has the most space to achieve it own energy minimum. Online 26 May 2005 |
Acta Cryst. (2005). D61, 750-754 [ doi:10.1107/S0907444905007110 ] Comparison of the crystallization and crystal packing of two Fab single-site mutant protein L complexesV. Granata, N. G. Housden, S. Harrison, C. Jolivet-Reynaud, M. G. Gore and E. A. SturaSynopsis: Tryptophans introduced in protein L (PpL) for stopped-flow fluorescence studies make crystal contacts when two different PpL mutants, Y64W and A66W are crystallized bound to an Fab'. The lattice parameters are almost identical in two crystallographic directions, but are significantly different in the third direction, showing that a small displacement of a contact residue is amplified in the lattice. Online 26 May 2005 |
Acta Cryst. (2005). D61, 755-758 [ doi:10.1107/S0907444905000405 ] Investigation of the protein pre-crystallization solution using analytical ultracentrifugationI. Yoshizaki, M. Sakai and Y. MatsuuraSynopsis: Analytical ultracentrifugation was used to study the crystal growth units in hen egg-white lysozyme pre-crystallization solution. Online 26 May 2005 |
Acta Cryst. (2005). D61, 759-762 [ doi:10.1107/S0907444905013466 ] Solution stirring initiates nucleation and improves the quality of adenosine deaminase crystalsH. Adachi, K. Takano, A. Niino, H. Matsumura, T. Kinoshita, M. Warizaya, T. Inoue, Y. Mori and T. SasakiSynopsis: A solution-stirring technique was used to obtain high-quality ADA complex and ADA native crystals. Online 26 May 2005 |
Acta Cryst. (2005). D61, 763-771 [ doi:10.1107/S0907444904028902 ] Extracting trends from two decades of microgravity macromolecular crystallization historyR. A. Judge, E. H. Snell and M. J. van der WoerdSynopsis: Trends were analyzed from two decades of microgravity crystallization history. It was found that dedicated microgravity missions increase the chance of success when compared with those where crystallization took place as a parasitic aspect of the mission. Online 26 May 2005 |
Acta Cryst. (2005). D61, 772-775 [ doi:10.1107/S0907444904028768 ] Optimizing protein crystal growth through dynamic seedingD.-Y. Zhu, Y.-Q. Zhu, Y. Xiang and D.-C. WangSynopsis: A dynamic seeding method different from the conventional methods in a non-equilibrium serial micro/macroseeding and its successful use in the optimization of the CutCm protein crystal growth are described. Online 26 May 2005 |
Acta Cryst. (2005). D61, 776-779 [ doi:10.1107/S0907444905014708 ] An attempt to increase the efficiency of protein crystal screening: a simplified screen and experimentsW. Gao, S. Li and R. BiSynopsis: A simplified screen has been designed based on the efficiency of crystallization conditions from different screens and relevant studies and results of test experiments have shown that it could improve the success rate of crystallization and reduce consumption. Online 26 May 2005 |
Acta Cryst. (2005). D61, 780-783 [ doi:10.1107/S0907444904034407 ] Anaerobic purification and crystallization to improve the crystal quality: ferredoxin II from Desulfovibrio gigasY.-C. Hsieh, M.-Y. Liu, J. Le Gall and C.-J. ChenSynopsis: Anaerobic crystallization of ferredoxin II from D. gigas. Online 26 May 2005 |
Acta Cryst. (2005). D61, 784-788 [ doi:10.1107/S0907444905007109 ] Crystal quality and differential crystal-growth behaviour of three proteins crystallized in gel at high hydrostatic pressureA. Kadri, B. Lorber, C. Charron, M.-C. Robert, B. Capelle, M. Damak, G. Jenner and R. GiegéSynopsis: Crystallization under pressure and in agarose gel of thaumatin and two lysozymes reveals specific effects that are correlated with alterations of the protein hydration shells. Online 26 May 2005 |
Acta Cryst. (2005). D61, 789-792 [ doi:10.1107/S0907444905007122 ] Effects of macromolecular impurities and of crystallization method on the quality of eubacterial aspartyl-tRNA synthetase crystalsA. Moreno, A. Théobald-Dietrich, B. Lorber, C. Sauter and R. GiegéSynopsis: Minute amounts of protein impurities alter the growth of aspartyl-tRNA synthetase crystals. With the purest enzyme, the best crystals are grown in environments where convection is reduced. Online 26 May 2005 |
Acta Cryst. (2005). D61, 793-798 [ doi:10.1107/S0907444905001368 ] Protein crystal perfection and its applicationJ. R. HelliwellSynopsis: The assessment of protein crystal perfection with X-rays is reviewed. Several X-ray diffraction physics applications with protein crystals that harness perfection are given. Applications in neutron protein crystallography are then described. Online 26 May 2005 |
Acta Cryst. (2005). D61, 799-802 [ doi:10.1107/S0907444905008085 ] Development of a novel ampholyte buffer for isoelectric focusing: electric charge-separation of protein samples for X-ray crystallography using free-flow isoelectric focusingS.-H. Kim, H. Miyatake, T. Ueno, T. Nagao and K. MikiSynopsis: A novel ampholyte buffer suitable for crystallization using the ProTeam FFE apparatus has been developed. This buffer is able to generate pH gradients owing to the use of low-molecular-weight electrolytes. Online 26 May 2005 |
Acta Cryst. (2005). D61, 803-808 [ doi:10.1107/S0907444905006578 ] Comparison of lysozyme structures derived from thin-film-based and classical crystalsE. Pechkova, V. Sivozhelezov, G. Tropiano, S. Fiordoro and C. NicoliniSynopsis: A report of the systematic comparison of crystal structures produced by the nanobiofilm template method and by the classical hanging-drop vapour-diffusion method. Online 26 May 2005 |
Acta Cryst. (2005). D61, 809-812 [ doi:10.1107/S0907444905006566 ] Investigating crystal-growth mechanisms with and without LB template: protein transfer from LB to crystalE. Pechkova, S. Fiordoro, D. Fontani and C. NicoliniSynopsis: In lysozyme crystal growth induced by a lysozyme thin-film template direct protein transfer appears to occur from the LB film into the crystal being formed, giving a possible explanation for the mechanisms involved in crystal nucleation and growth. Online 26 May 2005 |
Acta Cryst. (2005). D61, 813-818 [ doi:10.1107/S0907444905006943 ] Supersaturated lysozyme solution structure studied by chemical cross-linkingC. L. Hall, J. R. Clemens, A. M. Brown and L. J. WilsonSynopsis: Glutaraldehyde cross-linking followed by separation has been used to detect aggregates of chicken egg-white lysozyme (CEWL) in supersaturated solutions Online 26 May 2005 |
Acta Cryst. (2005). D61, 819-825 [ doi:10.1107/S090744490402949X ] Quantitative imaging by confocal scanning fluorescence microscopy of protein crystallization via liquid-liquid phase separationD. Vivarès, E. W. Kaler and A. M. LenhoffSynopsis: Metastable states such as liquid-liquid phase separation, aggregation and gelation can affect protein crystallization. Mixtures of PEG and a large model protein, glucose isomerase, have been studied to characterize the effect of a metastable liquid-liquid phase separation on protein crystallization. Online 26 May 2005 |
Acta Cryst. (2005). D61, 826-831 [ doi:10.1107/S0907444905013703 ] Surface morphology and kinetic properties in rapid growth of EAFP protein crystals investigated by atomic force microscopyS. Wang, G. Li, Y. Xiang, R.-H. Huang, Y. Zhang and D.-C. WangSynopsis: The surface morphology and kinetic properties of rapid growth of EAFP protein crystals are observed by atomic force microscopy. The characteristic pattern related to the rapid growth is discussed. Online 26 May 2005 |
Acta Cryst. (2005). D61, 832-836 [ doi:10.1107/S0907444905013569 ] van der Waals phase transition in protein solutionsP. R. Wills and D. J. WinzorSynopsis: The van der Waals equation of state for imperfect gases is applied to solutions of macromolecules, especially to explain the fluid-fluid phase transition in protein solutions. Due account is taken of dimerization owing to intermolecular attraction, hard-sphere and electrostatic repulsion, as well as excluded volume effects caused by inert co-solutes. Online 26 May 2005 |
Acta Cryst. (2005). D61, 837-843 [ doi:10.1107/S0907444905006487 ] Measurable characteristics of lysozyme crystal growthS. Gorti, E. L. Forsythe and M. L. PuseySynopsis: Physical processes that effect protein crystal growth velocities are discussed. In particular, methods that can be applied to determine the occurrence of kinetic roughening are evaluated. Online 26 May 2005 |
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