Crystallization and X-ray structural analysis of bifunctional nuclease TBN1
T. Koval1, P. Lipovova3, T. Podzimek3,4, J. Matousek4, J. Duskova2, T. Skalova2, A. Stepankova2, J. Hasek2 and J. Dohnalek1,2
1Institute
of Physics, Academy of Sciences of the Czech Republic,v.v.i., Na Slovance 2,182
21 Praha 8, Czech Republic,
2Institute
of Macromolecular Chemistry, Academy of Sciences of the Czech Republic,v.v.i.,
Heyrovskeho nam. 2, 162 06 Praha 6, Czech Republic
3Institute
of Chemical Technology, Technicka 5, 166 28 Praha 6, Czech Republic
4Institute
of Plant Molecular Biology, Biology Centre, Academy of Sciences of the Czech
Republic,v.v.i., Branisovska 31, 370 05 Ceske Budejovice, Czech Republic
koval.tomas@gmail.com
Bifunctional
nuclease TBN1 (UniProt sequence accession no. AM238701) from Solanum
lycopersicum is a Zn2+- dependent plant glycoprotein composed of
277 amino acids with a molecular mass of 31.6 kDa (about 37 kDa when
glycosylated). TBN1 belongs to plant nuclease I group. Nuclease I proteins are
Zn2+, Mg2+ or Ca2+ dependent and capable of cleaving both RNA
and DNA in single and double stranded forms with a preference for bonds
adjacent to adenine. They produce 5‘-mononucleotides as end products at pH
range 5.0 - 6.5. TBN1 also plays a considerable role in specific apoptotic
functions, vascular system development, stress
response and tissue differentiation in plants [1]. In addition, TBN1 exhibits anticancerogenic properties [2]. Therefore, a detailed
structural study of this enzyme can contribute to development of new drugs for
cancer, bacterial and viral disease treatment. Nuclease P1 from Penicillium
citrinum with 24% sequence identity, the structure of which is known (PDB
ID 1ak0) [3], is probably the closest structural homologue of TBN1.
Recombinant tomato
nuclease R-TBN1 was produced by heterologous
expression in Nicotiana benthamiana (tobacco)
leafs and purified to homogeneity [2]. Crystals with sufficient quality for
X-ray diffraction analysis was obtain after optimization from initial screening
using vapor diffusion crystallization method and combination of salt and
polymer in the crystallization conditions. The first diffraction experiments
were performed using an in house Gemini Enhanced Ultra diffractometer with the
Atlas CCD detector (Oxford Diffraction) and three different crystal
morphologies were identified (orthorhombic, rhombohedral and trigonal).
Datasets for structural analysis were collected at the synchrotron radiation
source BESSY II (
We gratefully
acknowledge support from Praemium Academiae of AS CR, Institution research plan
AVOZ10100521 of the Institute of Physics, Institution research plan
AV0Z50510513 of the Institute of Plant
Molecular Biology, Biology
Centre. The authors wish to thank Dr. U. Müller of the Helmholtz-Zentrum
Berlin, Albert-Einstein-Str. 15 for support at the beam line.
1. J. Matousek, P. Kozlova, L. Orctova, A. Schmitz, K. Pesina, O. Bannach, N. Diermann, G. Steger,
D. Riesner, Biol. CHem., 388, (2007), 1–13.
2. J. Matousek, T. Podzimek, P. Pouckova, J. Stehlik, J. Skvor, P. Lipovova, J. Matousek, Neoplasma, 57,
(2010), 339-348.
3. C. Romier, R. Dominguez, A. Lahm, O. Dahl, D. Suck, Proteins, 32, (1998), 414–424.
4. T.Koval, P. Lipovova, T. Podzimek, J. Matousek, J. Duskova, T. Skalova, A. Stepankova, J. Hasek,
J. Dohnalek, Acta. Cryst., F67, (2011), 124-128
5. G. M. Sheldrick, Acta Cryst., A64, (2008), 112-122