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Plant multifunctional nuclease TBN1 with unexpected phospholipase activity: structural study and reaction-mechanism analysis.
- Source :
-
Acta crystallographica. Section D, Biological crystallography [Acta Crystallogr D Biol Crystallogr] 2013 Feb; Vol. 69 (Pt 2), pp. 213-26. Date of Electronic Publication: 2013 Jan 16. - Publication Year :
- 2013
-
Abstract
- Type I plant nucleases play an important role in apoptotic processes and cell senescence. Recently, they have also been indicated to be potent anticancer agents in in vivo studies. The first structure of tomato nuclease I (TBN1) has been determined, its oligomerization and activity profiles have been analyzed and its unexpected activity towards phospholipids has been discovered, and conclusions are drawn regarding its catalytic mechanism. The structure-solution process required X-ray diffraction data from two crystal forms. The first form was used for phase determination; the second form was used for model building and refinement. TBN1 is mainly α-helical and is stabilized by four disulfide bridges. Three observed oligosaccharides are crucial for its stability and solubility. The active site is localized at the bottom of the positively charged groove and contains a zinc cluster that is essential for enzymatic activity. An equilibrium between monomers, dimers and higher oligomers of TBN1 was observed in solution. Principles of the reaction mechanism of the phosphodiesterase activity are suggested, with central roles for the zinc cluster, the nucleobase-binding pocket (Phe-site) and Asp70, Arg73 and Asn167. Based on the distribution of surface residues, possible binding sites for dsDNA and other nucleic acids with secondary structure were identified. The phospholipase activity of TBN1, which is reported for the first time for a nuclease, significantly broadens the substrate promiscuity of the enzyme, and the resulting release of diacylglycerol, which is an important second messenger, can be related to the role of TBN1 in apoptosis.
- Subjects :
- Animals
Catalytic Domain
Crystallization
Crystallography, X-Ray
Deoxyribonucleases metabolism
Humans
Mice
Multienzyme Complexes metabolism
Phospholipases metabolism
Plant Proteins metabolism
Structure-Activity Relationship
Deoxyribonucleases chemistry
Solanum lycopersicum enzymology
Multienzyme Complexes chemistry
Phospholipases chemistry
Plant Proteins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1399-0047
- Volume :
- 69
- Issue :
- Pt 2
- Database :
- MEDLINE
- Journal :
- Acta crystallographica. Section D, Biological crystallography
- Publication Type :
- Academic Journal
- Accession number :
- 23385457
- Full Text :
- https://doi.org/10.1107/S0907444912043697