1. Cloning, expression, purification, crystallization and preliminary X-ray diffraction of a lysine-specific permease fromPseudomonas aeruginosa
- Author
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Martin Caffrey, Declan A. Doyle, Dianfan Li, and Emmanuel Nji
- Subjects
Amino Acid Transport Systems ,Stereochemistry ,Molecular Sequence Data ,Lysine ,Biophysics ,Gene Expression ,Crystal structure ,Biology ,Crystallography, X-Ray ,medicine.disease_cause ,Biochemistry ,Chromatography, Affinity ,law.invention ,Metal ,Bacterial Proteins ,Structural Biology ,law ,Escherichia coli ,Genetics ,medicine ,Amino Acid Sequence ,Cloning, Molecular ,Crystallization ,Peptide sequence ,Permease ,Substrate (chemistry) ,Condensed Matter Physics ,Crystallization Communications ,visual_art ,Pseudomonas aeruginosa ,Chromatography, Gel ,visual_art.visual_art_medium ,bacteria - Abstract
The prokaryotic lysine-specific permease (LysP) belongs to the amino acid–polyamine–organocation (APC) transporter superfamily. In the cell, members of this family are responsible for the uptake and recycling of nutrients, for the maintenance of a constant internal ion concentration and for cell volume regulation. The detailed mechanism of substrate selectivity and transport of L-lysine by LysP is not understood. A high-resolution crystal structure would enormously facilitate such an understanding. To this end, LysP fromPseudomonas aeruginosawas recombinantly expressed inEscherichia coliand purified to near homogeneity by immobilized metal ion-affinity chromatography (IMAC) and size-exclusion chromatography (SEC). Hexagonal- and rod-shaped crystals were obtained in the presence of L-lysine and the L-lysine analogue L-4-thialysine by vapour diffusion and diffracted to 7.5 Å resolution. The diffraction data were indexed in space groupP21, with unit-cell parametersa= 169.53,b= 169.53,c= 290.13 Å, γ = 120°.
- Published
- 2014
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