Crystallographic Analysis of Metal-Ion Binding to Human Ubiquitin

被引:24
作者
Arnesano, Fabio [2 ]
Belviso, Benny Danilo [2 ]
Caliandro, Rocco [1 ]
Falini, Giuseppe [3 ]
Fermani, Simona [3 ]
Natile, Giovanni [2 ]
Siliqi, Dritan [1 ]
机构
[1] CNR, Ist Cristallog, I-70126 Bari, Italy
[2] Univ Bari A Moro, Dipartimento Farmacochim, I-70125 Bari, Italy
[3] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
关键词
metal binding sites; platinum; proteins; ubiquitin; X-ray crystallography; POLYUBIQUITIN CHAINS; CRYSTAL-STRUCTURE; 20S PROTEASOME; DNA-REPAIR; CELL-DEATH; COMPLEXES; POLYMORPHISM; INHIBITION; PROTEINS; SITE;
D O I
10.1002/chem.201001617
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The metal-binding ability of human ubiquitin (hUb) towards a selection of biologically relevant metal ions and complexes has been probed. Different techniques have been used to obtain crystals suitable for crystallographic analysis. In the first type of experiments, crystals of hUb have been soaked in solutions containing copper(II) acetate and two metallodrugs, Zeise salt (K[PtCl3(eta(2)-C2H4)]center dot H2O) and cisplatin (cis-[PtCl2(NH3)(2)]). The Zeise salt is used in a test for hepatitis, whereas cisplatin is one of the most powerful anticancer drugs in clinical use. The Zeise salt readily reacts with hUb crystals to afford an adduct with three platinum residues per protein molecule, Pt-3-hUb. In contrast, copper(II) acetate and cisplatin were found to be unreactive for contact times up to one hour and to cause degradation of the hUb crystals for longer times. In the second type of experiments, hUb was cocrystallized with a solution of copper(II) or zinc(II) acetate or cisplatin. Zinc(II) acetate gives, at low metal-to-protein molar ratios (8:1), crystals containing one metal ion per three molecules of protein, Zn-hUb(3) (already reported in previous work), whereas at high metal-to-protein ratios (70:1) gives crystals containing three Zn-II ions per protein molecule, Zn-3-hUb. In contrast, once again, copper(II) acetate and cisplatin, even at low metal-to-protein ratios, do not give crystalline material. In the soaking experiment, the Zeise anion leads to simultaneous platination of His68, Met1, and Lys6. Present and previous results of cocrystallization experiments performed with Zn-II and other Group 12 metal ions allow a comprehensive understanding of the metal-ion binding properties of hUb with His68 as the main anchoring site, followed by Met1 and carboxylic groups of Glu16, Glu18, Glu64, Asp21, and Asp32, to be reached. In the case of platinum, Lys6 can also be a binding site. The amount of bound metal ion, with respect to that of the protein, appears to be a relevant parameter influencing crystal packing.
引用
收藏
页码:1569 / 1578
页数:10
相关论文
共 70 条
[1]
PHENIX:: building new software for automated crystallographic structure determination [J].
Adams, PD ;
Grosse-Kunstleve, RW ;
Hung, LW ;
Ioerger, TR ;
McCoy, AJ ;
Moriarty, NW ;
Read, RJ ;
Sacchettini, JC ;
Sauter, NK ;
Terwilliger, TC .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2002, 58 :1948-1954
[2]
Ubiquitin interactions of NZF zinc fingers [J].
Alam, SL ;
Sun, J ;
Payne, M ;
Welch, BD ;
Blake, BK ;
Davis, DR ;
Meyer, HH ;
Emr, SD ;
Sundquist, WI .
EMBO JOURNAL, 2004, 23 (07) :1411-1421
[3]
Effect of neurotoxic metal ions on the proteolytic activities of the 20S proteasome from bovine brain [J].
Amici, M ;
Forti, K ;
Nobili, C ;
Lupidi, G ;
Angeletti, M ;
Fioretti, E ;
Eleuteri, AM .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2002, 7 (7-8) :750-756
[4]
[Anonymous], ANGEW CHEM
[5]
[Anonymous], ANGEW CHEM
[6]
Copper-Triggered Aggregation of Ubiquitin [J].
Arnesano, Fabio ;
Scintilla, Simone ;
Calo, Vincenza ;
Bonfrate, Elena ;
Ingrosso, Chiara ;
Losacco, Maurizio ;
Pellegrino, Teresa ;
Rizzarelli, Enrico ;
Natile, Giovanni .
PLOS ONE, 2009, 4 (09)
[7]
THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[8]
Novel T-shaped 14-electron platinum(II) complexes stabilized by one agostic interaction [J].
Baratta, W ;
Stoccoro, S ;
Doppiu, A ;
Herdtweck, E ;
Zucca, A ;
Rigo, P .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (01) :105-108
[9]
Structure, function, and amyloidogenesis of fungal prions: Filament polymorphism and prion variants [J].
Baxa, Ulrich ;
Cassese, Todd ;
Kajava, Andrey V. ;
Steven, Alasdair C. .
FIBROUS PROTEINS: AMYLOIDS, PRIONS AND BETA PROTEINS, 2006, 73 :125-+
[10]
Di-μ-chlorido-bis[chlorido(η2-ethene)platinum(II)] [J].
Boag, Neil M. ;
Ravetz, Megan S. .
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2007, 63 :M3103-U2208