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1.  Single-drop optimization of protein crystallization 
A device has been developed to optimize crystal-growth conditions by experiments in a single drop.
A completely new crystal-growth device has been developed that permits charting a course across the phase diagram to produce crystalline samples optimized for diffraction experiments. The utility of the device is demonstrated for the production of crystals for the traditional X-ray diffraction data-collection experiment, of microcrystals optimal for data-collection experiments at a modern microbeam insertion-device synchrotron beamline and of nanocrystals required for data collection on an X-ray laser beamline.
doi:10.1107/S1744309112024074
PMCID: PMC3412791  PMID: 22869140
crystal growth; single-drop optimization; Xtal-Controller
2.  Big changes are ahead – a new format for crystallization communications in Acta Cryst. F  
The Editors of Acta F look forward to 2014.
doi:10.1107/S1744309113031990
PMCID: PMC3855710  PMID: 24316820
2014; editorial
3.  Acta Crystallographica Section F: Structural Biology Communications  
Editorial.
doi:10.1107/S1744309113020873
PMCID: PMC3729152  PMID: 23908021
title change; editorial
4.  The future of crystallization communications in Acta Cryst. F  
Editorial.
doi:10.1107/S1744309113017909
PMCID: PMC3702310  PMID: 23832193
crystallization communications; editorial
6.  Crystals on the cover 2013 
Editorial.
doi:10.1107/S1744309112051950
PMCID: PMC3539692  PMID: 23295475
crystals; editorial
8.  Call for a crystallization ontology 
Editorial.
doi:10.1107/S174430911200680X
PMCID: PMC3310523  PMID: 22442215
crystallization ontology; editorial
9.  Efficient UV detection of protein crystals enabled by fluorescence excitation at wavelengths longer than 300 nm 
Excitation of intrinsic fluorescence at wavelengths longer than 300 nm is effective in the detection of protein crystals in crystallization trials set up in the most commonly used hardware.
It is well known that most proteins and many other biomolecules fluoresce when illuminated with UV radiation, but it is also commonly accepted that utilizing this property to detect protein crystals in crystallization setups is limited by the opacity of the materials used to contain and seal them. For proteins, this fluorescence property arises primarily from the presence of tryptophan residues in the sequence. Studies of protein crystallization results in a variety of setup configurations show that the opacity of the containment hardware can be overcome at longer excitation wavelengths, where typical hardware materials are more transparent in the UV, by the use of a powerful UV-light source that is effective in excitation even though not at the maximum of the excitation response. The results show that under these circumstances UV evaluation of crystallization trials and detection of biomolecular crystals in them is not limited by the hardware used. It is similarly true that a deficiency in tryptophan or another fluorescent component that limits the use of UV light for these purposes can be effectively overcome by the addition of fluorescent prostheses that bind to the biomolecule under study. The measurements for these studies were made with a device consisting of a potent UV-light source and a detection system specially adapted (i) to be tunable via a motorized and software-controlled absorption-filter system and (ii) to convey the excitation light to the droplet or capillary hosting the crystallization experiment by quartz-fibre light guides.
doi:10.1107/S1744309110007153
PMCID: PMC2852349  PMID: 20383027
UV fluorescence; detection of protein crystals
10.  Crystals on the cover 2012 
Editorial.
doi:10.1107/S1744309111053759
PMCID: PMC3253823  PMID: 22232160
crystals; editorial
12.  Editorial 
Editorial.
doi:10.1107/S1744309110053959
PMCID: PMC3079961
crystals; editorial
13.  Citations in supplementary material 
The problem of undercounting of citations that are published only in supplementary material is studied for the journals Nature, Science, Cell and the Proceedings of the National Academy of Sciences (USA).
doi:10.1107/S1744309110041825
PMCID: PMC2998352  PMID: 21139193
citations; supplementary material; editorial
18.  Crystals on the cover for 2009 
doi:10.1107/S1744309108043224
PMCID: PMC2628857  PMID: 19153444
Editorial
21.  Editorial 
doi:10.1107/S174430910601774X
PMCID: PMC2243099
Editorial

Results 1-25 (27)