Title : De novo sulfur SAD phasing of the lysosomal 66.3 kDa
protein from mouse
Abstract :
- The 66.3 kDa protein from mouse is a soluble protein of the lysosomal matrix
- It is synthesized as a glycosylated 75 kDa preproprotein which is further processed into 28 and 40 kDa fragments
- Despite bioinformatics approaches and molecular characterization of the 66.3 kDa protein , the mode of its maturation as well as its physiological function remained unknown
- Therefore, it was decided to tackle this question by means of X-ray crystallography
- After expression in a human fibrosarcoma cell line, the C-terminally His-tagged single-chain 66.3 kDa variant and the double-chain form consisting of a 28 kDa fragment and a 40 kDa fragment were purified to homogeneity but could not be separated during the purification procedure
- This mixture was therefore used for crystallization
- Single crystals were obtained and the structure of the 66.3 kDa protein was solved by means of sulfur SAD phasing using data collected at a wavelength of 1.9 A on the BESSY beamline BL14.2 of Freie Universität Berlin
- Based on the anomalous signal, a 22-atom substructure comprising 21 intrinsic S atoms and one Xe atom with very low occupancy was found and refined at a resolution of 2.4 A using the programs SHELXC/D and SHARP
- Density modification using SOLOMON and DM resulted in a high-quality electron-density map, enabling automatic model building with ARP / wARP
- The initial model contained 85% of the amino-acid residues expected to be present in the asymmetric unit of the crystal
- Subsequently, the model was completed and refined to an R(free) factor of 19.8%
- The contribution of the single Xe atom to the anomalous signal was analyzed in comparison to that of the S atoms and was found to be negligible
- This work should encourage the use of the weak anomalous scattering of intrinsic S atoms in SAD phasing, especially for proteins, which require both expensive and time-consuming expression and purification procedures, preventing extensive screening of heavy-atom crystal soaks
Output (sent_index, trigger,
protein,
sugar,
site):
- 2. glycosylated, , preproprotein, -, -
Output(Part-Of) (sent_index,
protein,
site):
*Output_Site_Fusion* (sent_index,
protein,
sugar,
site):