The Cu-binding site in the [Cu·dCMP·dCMP-H] ^1- complex was investigated. The tandem mass (MS/MS) spectra of the [Cu·dCMP·dCMP-H] ^1- parent ion showed [dCMP·Cu·H ₂ PO ₄ +CONH] ^1- fragmentions. Therefore, we propose that the Cu cation is simultaneously coordinated to the phosphate site and cytosine moiety in the stable geometry of the [Cu·dCMP·dCMPH] ^1- complex. Three geometries for the complex were considered in an attempt to optimize the structure of the [Cu·dCMP·dCMP-H] ^1- complex. The ab initio calculations were performed at the B3LYP/6-311G ^** level. The interactions of metal cations with DNA, as a part of a [M·DNA] complex, have been studied extensively using IR, 1 X-ray, 2 and other techniques. 3 Metal cations can both stabilize and destabilize DNA; 4 they prefer to interact with the phosphate anions in the backbone of DNA by nonspecific electrostatic attraction, which stabilizes the DNA helix structure. 1 , 5 However, several divalent metal cations destabilize DNA and decrease the mean transition temperature (T _m ) of DNA. 4 In particular, Cu cations substantially decrease the T _m of DNA. 4 Cu cations are regarded to be effective in destroying the native structure of DNA. In contrast to Cu cations, Mg cations increase the T _m of DNA and stabilize DNA. The structures of [M·(nucleoside monophosphate)] complexes have been investigated to evaluate the effect of metal cations on the structure of the [M·DNA] complex. 6 - 11 Metal cations prefer the phosphate anions; however, several complexperimental results showed that the base moieties had also been regarded as the preferred binding sites in the formation of [M·(nucleoside monophosphate)] complexes. As a member of [M·(nucleoside monophosphate)] complexes, [M·dCMP] (dCMP = deoxycytidine monophosphate) complexes have been extensively studied. 7 - 11 A local pentacoordinated tetragonal pyramid geometry with a coordination of one N atom (cytosine) and four O atoms has been observed by the powder EPR spectrum of [Cu·CMP] complex. 7 The metal binding sites of the [M·H·dCMP] ¹⁺ (M = Mg ²⁺ , Cu ²⁺ ) complex has been observed in the aqueous solution; 10 the metal cation was mainly located at the N3 (cytosine) atom, as determined by the acidity constant analysis using potentiometric pH titrations. However, the coordination chemistry between Cu cation and nucleic acid building block such as nucleotides, is rather scarcely documented in gas-phase. In this study, we have focused our attention on the formation and fragmentation pattern of gas-phase [dCMP] ^1- and [M·dCMP·dCMP-H] ^1- (M = Mg ^{2 +} , Cu ²⁺ ) complexes using ESI-MS and tandem mass spectrometry (MS/MS) methods. The [dCMP] ^1- and [M·dCMP·dCMP-H] ^1- complexperimental exes were formed in the solution and electrosprayed on the quadrupole ion guide using nitrogen gas. Intact gas-phase [dCMP] ^1- and [M·dCMP·dCMP-H] ^1- complex ions were expected in the ESI-MS spectra. 12 - 14 An Ab initio calculation was performed to explain the geometry and stabilization energy of the [Cu·dCMP·dCMP-H] ^1- complex ion. Intact gas-phase [dCMP] ^1- or [M·dCMP·dCMP-H] ^1- (M = Mg ²⁺ , Cu ²⁺ ) ion was formed by the ESI-MS method. The experimental MS and MS/MS data for the fragmentation pattern analysis were obtained using a Thermo Finnigan LTQ mass spectrometer (Thermo Electron Corporation, San Jose, CA, USA). The LTQ mass spectrometer conditions have reported in the previous study. 15 The reagents used are as follows: dCMP (2’-deoxycytidine 5’-monophosphate 98%, Sigma-Aldrich, Korea), CuCl ₂ (99.999%, Sigma-Aldrich, Korea), MgCl ₂ (99.99%, Sigma-Aldrich, Korea), H ₂ O (HPLC grade, Merck), and D ₂ O (99.9 atom%, Sigma-Aldrich, Korea). dCMP was dissolved in H ₂ O (or D ₂ O) to prepare a 4×10 ^-5 M solution. CuCl ₂ was dissolved in H ₂ O (or D ₂ O) to prepare a 4×10 ^-4 M solution. The [dCMP + metal] solutions were mixed prior to the mass spectral analyses. The ab initio calculations were performed using 6-311G ^** basis sets to determine the optimized structures and energies. The density functional theory (DFT) calculations at the B3LYP level were carried out using the Gaussian09 series program. DFT was chosen because it is less computationally demanding than the other computational methods with a similar accuracy for the ground-state energy calculations. 16 The vibrational frequencies were also calculated at the B3LYP level to confirm the optimized geometries corresponding to the true minima on the potential energy surface. The structures of [dCMP] ^1- and three [Cu·dCMP·dCMPH] ^1- complexes are shown in Fig. 1 . A copper ion is located in the center of two dCMP molecules because of the basicity of the corresponding phosphate groups. Complexes 1 and 2 show a square planar geometry, where the Cu cation is tetra-coordinated to the four O atoms in Complex 1, or two O and two N atoms in Complex 2. Complex 3 showed a tetragonal pyramid geometry, where the Cu cation is penta-coordinated to the five O atoms. The N3 atom of cytosine in dCMP is indicated as a part of the [Cu...dCMP] coordination in Fig. 1 c. Four MS/MS spectra are shown in Fig. 2 . In the MS/MS spectrum of [dCMP] ^1- ion ( Fig. 2 a), the fragmentions at m/z 263, 195, and 97 were observed under the low-energy CID experimental conditions. The ions at m/z 263 and 195 were assigned to the loss of CONH and cytosine fragments in the parent [dCMP] ^1- ion, respectively. The low-energy CID MS/MS results of the four parent ions are summarized in Table 1 . The CONH loss dissociation channel of the [dCMP] ^1- ion is indicated as the ‘B’ bond dissociation in Fig. 1 a loss dissociation channel of the cytosine part has been reported in the MS/MS spectrum of the [Cu·Cyt·Gua-H] ¹⁺ ion. 15 The fragmention at m/z 97 was assigned to a [306-dC + 18] ^1- ion, which corresponded to a [H ₂ PO ₄ ] ^1- ion. The added 18 amu may be attributed to the (OH group + H atom), able to be associated to the PO ₃ group. The formation of the fragmention at m/z 97 may be alternatively caused by the ‘A1’ bond dissociation ( Fig. 1 a). The fragmention at m/z 97 in this dissociation process may be attributed to a [306 − (dC − O) + 2H] ¹⁻ ion, which still corresponded to a [H ₂ PO ₄ ] ¹⁻ ion. The (OH group + H atom) dissociation process from the phosphate group has been reported by Strittmatter et al . 17 The MS/MS spectrum of the [Mg·dCMP·dCMP-H] ¹⁻ complex ( m/z 635) shows two main fragments, m/z 306 and 408, corresponding to a [dCMP] ¹⁻ ion and a dC-loss fragmention, respectively, as shown in Fig. 2 b. Each dissociation channel is indicated as the ‘D’ or ‘E’ bond dissociation in Fig. 2 b. A fragmention at m/z 425, a [635 − dC + 18] ¹⁻ ion, which was observed in a low intensity corresponded to a [dCMP·Mg·H ₂ PO ₄ ] ¹⁻ ion. Two fragmentions, [306 − dC + 18] ¹⁻ ion ( Fig. 2 a) and [635 − dC + 18] ¹⁻ ion ( Fig. 2 b), may have originated from a similar dissociation process. Based on the observation in Fig. 2 b, Complex 1 geometry (dCMP...Mg...dCMP) should be regarded as a stable geometry in the [Mg·dCMP·dCMP-H] ¹⁻ complex. 18 Fig. 2 c shows the MS/MS spectrum of the parent [Cu·dCMP·dCMP-H] ¹⁻ ( m/z 674) ion. Interestingly, a [674 − dC + 18 + CONH] ¹⁻ fragmention at m/z 508 was observed, which corresponded to the [dCMP·Cu·H ₂ PO ₄ + CONH] ¹⁻ ion. This dissociation channel of the cytosine CONH moiety (‘B’ in Fig. 1 a) was not observed in the MS/MS spectrum of the [Mg·dCMP·dCMP-H] ¹⁻ ion ( Fig. 2 b). Therefore, the CONH moiety may be associated to the central Cu cation in the [Cu·dCMP·dCMP-H] ¹⁻ complex. For the analysis of the association of the CONH moiety (+CONH) to the [674 − dC + 18] ¹⁻ fragment, the geometry of Complex 2 or 3 was proposed as the stable structure for the [Cu·dCMP·dCMPH] ¹⁻ ion ( Fig. 1 ). The cytosine N3 or O2 atom was indicated as the participating ligand in the [Cu...dCMP] coordination in the geometry of Complex 2 or 3. The participation of cytosine N3 atom in the [Cu...dCMP] coordination has been proposed by the powder EPR spectrum of the Cu-5’-CMP complex. 11 The participation of cytosine N3 or O2 atom in the [metal...dCMP] coordination structure has also been analyzed in the structure of the [Pb·dCMP-H] ¹⁺ complex. 11 Other main MS/MS fragmentions of the parent [Cu·dCMP·dCMP-H] ¹⁻ ( m/z 674) ion were observed at m/z 465, 447, and 306 corresponding to [674 − dC + 18] ¹⁻ , [674 − dC] ¹⁻ , and [dCMP] ¹⁻ , respectively ( Fig. 2 c). These fragmention analysis was supported by a D ₂ O experiment from the observation of m/z 469 (470), 450, and 310 corresponding to [681 − dC _deu + 19] ¹⁻ ([681 − dC _deu + 20] ¹⁻ ), [681 − dC _deu ] ¹⁻ , and [dCMP _deu ] ¹⁻ , respectively ( Fig. 2 d). Seven possible hydrogen atoms existed, as shown in Complex 2 or 3, for the H/D deuteration process in the [Cu·dCMP·dCMP-H] ¹⁻ ( m/z 674) complex. Therefore, the [Cu·dCMP _deu ·dCMP _deu -D] ¹⁻ ( m/z 681) ion was selected as the parent ion in the MS/MS spectrum ( Fig. 2 d). The peak at m/z 513 was assigned as a [681 − dC _deu + 19 + COND] ¹⁻ ion ( Table 1 ) because of the higher intensity of m/z 469 ([681 − dC _deu +19] ¹⁻ ion) than that of m/z 470 ([681 − dC _deu + 20] ¹⁻ ion) ( Fig. 2 d). In order to know the stability of the [Cu·dCMP·dCMP- H] ¹⁻ complex ion, we tried to optimize the geometries of Complexes 1-3 by the ab initio calculations. The relative SCF energies for Complexes 1-3 are listed in Table 2 , as the energy difference from Complex 1. The energy differences were in a − 15.4 to − 10.1 kcal/mol range based on the gas-phase B3LYP/6-311G ^** calculations. Complex 2 was the most stable structure among the optimized [Cu·dCMP·dCMP-H] ¹⁻ complexes. Three structures (Complex 1-3) may have been formed simultaneously in (Cu + dCMP) solution in conformity to the similar SCF energies of the three [Cu·dCMP·dCMP-H] ¹⁻ optimized complexes. Similarly, the negative charge character of the cytosine N3 atom can be compared to that of the phosphate group O atom in the [dCMP] ¹⁻ ion. In the geometry optimized [dCMP] ¹⁻ ion, the atomic charges (phosphate group O atoms, cytosine N3, and cytosine O2) were calculated in the range from −0.7 to −0.4 ( Table 3 ). The planar geometries (Cu-O ₁ O ₂ O ₃ O ₄ for Complex 1, Cu-O ₁ N ₂ O ₃ N ₄ for Complex 2, and Cu-O ₁ O ₂ O ₃ O ₄ for Complex 3) were observed for the small dihedral angles in the geometry optimization of the [Cu·dCMP·dCMP− H] ¹⁻ complex. The optimized parameters such as bond distances and dihedral angles are listed in Table 4 . The dihedral angles, O ₁ -O ₂ -O ₃ -O ₄ (−0.4 ^o ) for Complex 1 and O ₁ -N ₂ -O ₃ -N ₄ (−4.4 ^o ) for Complex 2, were almost zero. The structure of complex 3 (Cu- O ₁ O ₂ O ₃ O ₄ O ₅ ) was optimized to a tetragonal pyramidal geometry ( Fig. 1 d). A fifth ligand (the cytosine O2 atom, O ₅ ) was added to the four-coordination (Cu-O ₁ O ₂ O ₃ O ₄ ) geometry in the tetragonal pyramidal geometry. The carbonyl oxygen atom (O ₅ ) of cytosine was located at the apex of the optimized tetragonal pyramidal geometry. A small deviation from the planar structure of Complex 3 was observed in the dihedral angles, O ₁ -O ₂ -O ₃ -O ₄ (− 12.9 ^o ) and O ₁ -O ₂ -O ₃ -Cu (12.0 ^o ) ( Table 4 ). The Cu-binding site in the [Cu·dCMP·dCMP-H] ¹⁻ complex was investigated. In the MS/MS spectrum of the [Cu·dCMP·dCMP-H] ¹⁻ complex, the [dCMP·Cu·H ₂ PO ₄ + CONH] ¹⁻ fragmention was observed as the main fragmention. Based on the direct interaction between the Cu cation and CONH in the [dCMP·Cu·H ₂ PO ₄ + CONH] ¹⁻ fragmention, we proposed that the Cu cation is bound simultaneously to the cytosine (N3 or O2) and a phosphate group. The simultaneous coordination of Cu cation to the phosphate site and cytosine moiety (Complex 2 or 3) was supported by the SCF energy calculations of the geometry optimized [Cu·dCMP·dCMPH] ¹⁻ complexes.