Crystallization of the pneumococcal autolysin LytC: in-house phasing using novel lanthanide complexes

被引:4
作者
Perez-Dorado, Inmaculada [1 ]
Sanles, Reyes [1 ]
Gonzalez, Ana [2 ]
Garcia, Pedro [2 ]
Garcia, Jose L. [2 ]
Martinez-Ripoll, Martin [1 ]
Hermoso, Juan A. [1 ]
机构
[1] CSIC, Grp Cristalog Macromol & Biol Estructural, Inst Quim Fis Rocasolano, E-28006 Madrid, Spain
[2] CSIC, Dept Mol Microbiol, Ctr Invest Biol, E-28040 Madrid, Spain
来源
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS | 2010年 / 66卷
关键词
autolysins; LytC; Gd-HPDO3A; STREPTOCOCCUS-PNEUMONIAE; MACROMOLECULAR CRYSTALLOGRAPHY; PROTEINS; ENZYMES; CBPF;
D O I
10.1107/S1744309110006081
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
LytC, one of the major autolysins from the human pathogen Streptococcus pneumoniae, has been crystallized as needles by the hanging-drop technique using 10%(w/v) PEG 3350 as precipitant and 10 mM HEPES pH 7.5. LytC crystals were quickly soaked in mother liquor containing 2 mM of the complex Gd-HPDO3A to produce derivatized crystals (LytC(Gd-HPDO3A)). Both native LytC and isomorphous LytC(Gd-HPDO3A) crystals were flash-cooled in a nitrogen flow at 120 K prior to X-ray data collection using an in-house Enraf-Nonius rotating-anode generator (lambda = 1.5418 A) and a MAR345 imaging-plate detector. In both cases, good-quality diffraction patterns were obtained at high resolution. LytC(Gd-HPDO3A) crystals allowed the collection of a SAD X-ray data set to 2.6 A resolution indexed in terms of a P2(1) monoclinic unit cell with parameters a = 59.37, b = 67.16, c = 78.85 A, beta = 105.69 degrees. The anomalous Patterson map allowed the identification of one heavy-atom binding site, which was sufficient for the calculation of an interpretable anomalous map at 2.6 A resolution.
引用
收藏
页码:448 / 451
页数:4
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