Synthesis, Antiproliferative Activity, and DNA Binding Studies of Nucleoamino Acid-Containing Pt(II) Complexes

We here report our studies on the reaction with the platinum(II) ion of a nucleoamino acid constituted by the l-2,3-diaminopropanoic acid linked to the thymine nucleobase through a methylenecarbonyl linker. The obtained new platinum complexes, characterized by spectroscopic and mass spectrometric techniques, were envisaged to exploit synergistic effects due to the presence of both the platinum center and the nucleoamino acid moiety. The latter can be potentially useful to protect the complexes from early deactivation, as well as to facilitate their cell internalization. The biological activity of the complexes in terms of antiproliferative effects was evaluated in vitro on different cancer cell lines and healthy cells, showing the best results on human cervical adenocarcinoma (HeLa) cells along with good selectivity for cancer over normal cells. In contrast, the metal-free nucleoamino acid did not show any cytotoxicity on both normal and cancer cell lines. Finally, the ability of the novel Pt(II) complexes to bind various DNA model systems was investigated by circular dichroism (CD) spectroscopy and polyacrylamide gel electrophoresis analyses proving that the newly obtained compounds can potentially target DNA, similarly to other well-known anticancer Pt complexes, with a peculiar G-quadruplex vs. duplex selectivity.


Introduction
Cisplatin (cis-diaminedichloro-platinum, CDDP) is one of the most active chemotherapeutic agents used for the treatment of a large variety of malignancies, especially testicular and ovarian carcinomas, even if its clinical utility is restricted by both toxicological and tumor resistance drawbacks [1,2]. CDDP activity and toxicity is mainly due to DNA binding [3,4], occurring via both inter-and intrastrand crosslinks, that suppresses DNA replication and also RNA transcription. Specifically, CDDP interacts with the DNA nucleobases forming stable platinum-nitrogen covalent bonds, which lead to irreversible adducts responsible for cisplatin antitumor activity [1,4].
The drawbacks and side effects of cisplatin treatment [1,2] have stimulated the design and synthesis of new anticancer Pt-based drugs with the aim of obtaining compounds more effective and Considering the capability of the platinum ion to bind both nucleobases and amino acids, our novel design consisted of Pt(II) complexes, incorporating as ligands nucleoamino acids, constituted by nucleobases linked to an amino acid through a suitable linker (Figure 1b), and thus, intrinsically containing various potential platinum binding sites. To the best of our knowledge, this is the first report on Pt complexes incorporating this kind of ligand. Nucleoamino acids have been widely explored in the literature, mainly as building blocks for the assembly of nucleopeptides, compounds potentially able to bind complementary nucleic acids in antisense/antigene strategies, or to give ordered self-assembly, a useful property in the context of the development of new nanomaterials [25][26][27][28][29][30][31]. Considering the capability of the platinum ion to bind both nucleobases and amino acids, our novel design consisted of Pt(II) complexes, incorporating as ligands nucleoamino acids, constituted by nucleobases linked to an amino acid through a suitable linker (Figure 1b), and thus, intrinsically containing various potential platinum binding sites. To the best of our knowledge, this is the first report on Pt complexes incorporating this kind of ligand. Nucleoamino acids have been widely explored in the literature, mainly as building blocks for the assembly of nucleopeptides, compounds potentially able to bind complementary nucleic acids in antisense/antigene strategies, or to give ordered self-assembly, a useful property in the context of the development of new nanomaterials [25][26][27][28][29][30][31].
Recently, a 9-fluorenylmethoxycarbonyl (Fmoc)-protected nucleoamino acid, obtained connecting the Fmoc-diaminopropanoic acid (Fmoc-DAP-OH) to the thymine acetic acid, was synthesized in our group and then used to obtain, via solid-phase peptide synthesis, a homothymine nucleopeptide for potential biomedical applications [30].
Here we used the deprotected DAP(T)-OH nucleoamino acid for platinum complexation to obtain new Pt complexes in which synergistic anticancer effects were envisaged for the presence of both the nucleobase and the platinum center. The selected nucleoamino acid contained several donor groups for platinum (i.e., the nitrogen atoms of the α-amino group, the nucleobase, or the amide in the methylenecarbonyl linker, and the oxygens of the carboxylic function of the nucleoamino acid) and could potentially form a large variety of Pt complexes. The compounds obtained from the platination reaction of DAP(T)-OH were purified and characterized by nuclear magnetic resonance (NMR), mass spectrometry, and ultraviolet-visible (UV-vis) techniques. Then, the antiproliferative activity of the new Pt(II) complexes was evaluated in preliminary tests on different cancer cell lines and normal human cells, using the starting nucleoamino acid as a reference compound. Finally, in analogy to other metal complexes, the ability of the new Pt(II) complexes to bind DNA was also explored using circular dichroism (CD) and polyacrylamide gel electrophoresis analyses on different DNA model systems, both in random coil and in structured forms.

Platination of the DAP(T)-Based Nucleoamino Acid
Analogously to previous works [5,12], the platination reaction was carried out mixing DAP(T)-OH (4, Scheme 1), as a Pt chelator, and K 2 PtCl 4 in CH 3 OH:H 2 O (9:1, v/v) under stirring at room temperature in the dark. Subsequently, the solvent was removed under vacuum at low temperature, and the dried crude was sequentially treated with various organic solvents (see Materials and Methods) to dissolve the yellow solid. In detail, a solid-liquid extraction, followed by washings and centrifugations, using not significantly coordinating solvents with increasing polarity (CH 2 Cl 2 , CHCl 3 , CH 3 COCH 3 , CH 3 OH, H 2 O), was performed. Neither the apolar solvents (CH 2 Cl 2 , CHCl 3 ) nor acetone were able to dissolve the solid allowing the recovery of the Pt complexes. In contrast, methanol was able to solubilize and recover a yellow product and, subsequently, H 2 O dissolved the second and last complex (see Materials and Methods).

Platination of the DAP(T)-Based Nucleoamino Acid
Analogously to previous works [5,12], the platination reaction was carried out mixing DAP(T)-OH (4, Scheme 1), as a Pt chelator, and K2PtCl4 in CH3OH:H2O (9:1, v/v) under stirring at room temperature in the dark. Subsequently, the solvent was removed under vacuum at low temperature, and the dried crude was sequentially treated with various organic solvents (see Materials and Methods) to dissolve the yellow solid. In detail, a solid-liquid extraction, followed by washings and centrifugations, using not significantly coordinating solvents with increasing polarity (CH2Cl2, CHCl3, CH3COCH3, CH3OH, H2O), was performed. Neither the apolar solvents (CH2Cl2, CHCl3) nor acetone were able to dissolve the solid allowing the recovery of the Pt complexes. In contrast, methanol was able to solubilize and recover a yellow product and, subsequently, H2O dissolved the second and last complex (see Materials and Methods).
The two obtained products were subjected to LC-ESI-MS analysis, showing a single chromatographic peak in the total ion current (TIC) profile of the injection performed immediately after their dissolution (t = 0, Figure S4a, left) with a complex mass spectrum denoting fragmentation during the ionization process ( Figure S4a, right). Both the complexes showed almost the same peaks in the mass spectrum, evidencing that they followed the same fragmentation pattern and could probably be isomers (as an example, in Figure S4, we reported the LC-ESI-MS analysis of the methanol-recovered complex). From the analysis of the mass peaks of the complexes ( Figure S4a, The two obtained products were subjected to LC-ESI-MS analysis, showing a single chromatographic peak in the total ion current (TIC) profile of the injection performed immediately after their dissolution (t = 0, Figure S4a, left) with a complex mass spectrum denoting fragmentation during the ionization process ( Figure S4a, right). Both the complexes showed almost the same peaks in the mass spectrum, evidencing that they followed the same fragmentation pattern and could probably be isomers (as an example, in Figure S4, we reported the LC-ESI-MS analysis of the methanol-recovered complex). From the analysis of the mass peaks of the complexes ( Figure S4a, right), we could hypothesize that they both contained in their structures a DAP(T)-OH unit, platinum(II) and chloride ions, and a water molecule. The injection performed 10 min after the dissolution of both the compounds showed at least three peaks in the TIC profiles, each associated with a mass spectrum very difficult to interpret, evidencing that the Pt complexes are very unstable in aqueous solutions ( Figure S4b) and, thus, difficult to handle for both their characterization and subsequent in vitro assays.
Then, since the most commonly used NMR organic solvents (CDCl 3 , CD 3 OD, CD 3 COCD 3 ) were not able to solubilize the two products at the minimum concentration required for a complete NMR characterization, we decided to dissolve the complexes in a highly solubilizing solvent, such as N,N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO). Even if these solvents are well known to trigger exchange reactions with various Pt(II) ligands (see [5,15] for DMSO and [13] for DMF), in many cases, DMSO moieties were intentionally inserted in various bioactive platinum complexes to Pharmaceuticals 2020, 13, 284 5 of 20 increase their activity and stability [5,15]. The compounds obtained after DMSO treatment (Scheme 1) were named T1 and T2. They were derived, respectively, from the Pt complexes originally recovered with CH 3 OH and H 2 O.
As expected, in the ESI mass spectra (positive ion-mode) of the DMSO-solubilized complexes, we effectively verified the occurrence of the exchange reaction realized by the solvent. Indeed, for both complexes, the found mass peaks were attributed to molecules containing a DAP(T)-OH unit, a platinum(II) ion, a chloride ion, and a DMSO molecule (m/z ca. 579, Figure S5a), indicating that the two complexes were either constitutional or geometrical isomers. In the recorded mass spectra, T1-and T2-adducts with Na + and K + ions were also found, respectively, at ca. 601 and 617 m/z ( Figure S5a).
The peak isotopic distribution for each species found in the mass spectra of the two isomers was almost superimposable to the theoretical one calculated with the Isotope Distribution Calculator program (http://www.sisweb.com/mstools/isotope.htm). As an example, we reported the comparison between the theoretical and experimental peak at ca. 579 m/z of T1 ( Figure S5b).
To verify how the nucleoamino acid ligand coordinated the platinum(II) ion in these isomers, mono-and bi-dimensional NMR experiments were carried out, recording all the spectra in DMSO-d 6 ( Figures S6-S8). The 1 H and 13 C-NMR spectra of DAP(T)-OH were used as references to evaluate the shifts of the corresponding signals in the complexes, thus obtaining information on the atoms directly involved in the coordination or influenced in their spectral properties by the proximity to the metal center. In Table 1, the 1 H and 13 C NMR chemical shift values for T1 and T2 were reported in comparison to the starting ligand. Assignments were based on correlation spectroscopy (COSY), heteronuclear single quantum correlation (HSQC), and heteronuclear multiple-bond correlation (HMBC) experiments (Tables S1-S3). In particular, in the 1 H NMR spectra of T1 and T2 complexes, two signals, i.e., broad multiplets at 5.68 and 6.29 ppm (for T1, Figure S6, up) and 5.63 and 6.25 ppm (for T2, Figure S7), were diagnostic of protons belonging to a nitrogen bound to platinum(II) center, in accordance with other complexes reported in the literature [32]. The two amino protons, equivalent and easily exchangeable in the starting compound, became not equivalent and not easily exchangeable when the α-amino group Pharmaceuticals 2020, 13, 284 6 of 20 coordinated the Pt ion. In addition, both proton and carbon signals of the CH-α (indicated as E) in T1 and T2 were markedly downfield shifted with respect to the corresponding signal in the starting amino acid (Table 1), indicating the presence of platinum in the proximity of this group. In the 13 C NMR spectra of both complexes, a downfield shift from 168 to about 181 ppm of the carboxylic carbon F was observed, indicating the coordination of the carboxylic group to the metal center. Strong evidence of the presence of DMSO as a platinum ligand in both Pt complexes came from new proton and carbon signals in T1 and T2, attributable to the methyl groups linked to the Pt-bound sulfur (downfield-shifted with respect to free DMSO), in agreement with chemical shifts reported in the literature for DMSO-containing Pt complexes [5,15].
Notably, in the explored conditions, only for T1 and not for T2, the presence of two rotamers (doubling of some proton/carbon signals) was observed. Rotamers, which are generally reported for peptide nucleic acid (PNA) or some nucleoamino acid monomers [33,34], are due to a restricted rotation around the amide bond. Thus, it can be deduced that the rotation of the nucleobase around the methylene group occurred more rapidly for T2 than for T1 in the NMR time scale.
All the NMR data indicated that both complexes coordinate platinum through the α-NH 2 and α-COOH groups, whereas the nucleobase, the methylenecarbonyl linker, and the amidic nitrogen were not involved in the metal center complexation. Thus, T1 and T2 can differ only for the relative position of the DMSO and chloride ligands. To confirm the exact position of these ligands in T1 and T2, nuclear Overhauser effect spectroscopy (NOESY) experiments were also performed. A diagnostic cross peak between the proton of the amino group coordinating the platinum and the DMSO-methyl groups was found in T2 NOESY spectrum but not in T1 (Table S4 and Figure S9). Finally, molecular modeling analysis of the Pt complexes, by applying the MMFF94 energy minimization method [35,36], confirmed the observed NOESY correlations (Figures S10 and S11, realized using the MOLVIEW program [35]). Taken together, the obtained data concurred to define for T1 and T2 the structures reported in Scheme 1, whereas for the initially obtained complexes, we hypothesize the structures depicted in Figure S11 (bottom).
To definitively confirm the structures of T1 and T2, as well as of their precursors, we tried to crystalize them in different ways to perform X-ray diffraction studies. Unfortunately, attempts to obtain good quality crystals were unsuccessful, and only decomposition products were observed.

UV-Vis Analysis of T1 and T2 Platinum Complexes in Aqueous Solution
Before analyzing the UV-vis behavior of T1 and T2 in aqueous solution, we first characterized the absorption spectral properties of the starting nucleoamino acid DAP(T)-OH. The UV spectrum of DAP(T)-OH, dissolved at 80 µM conc. in PBS (phosphate-buffered saline, 137 mM NaCl, 2.7 mM KCl, 10 mM Na 2 HPO 4 , 1.8 mM KH 2 PO 4 ), showed an intense band at 268 nm, characteristic of the thymine nucleobase (ε 260 = 8560 M −1 cm −1 ) [37]. The UV signal was monitored over time up to 96 h. Apart from a very slight increase in the 268-nm band in the first 24 h, no significant spectral changes were observed over a longer monitoring time, indicating good stability of DAP(T)-OH in the tested buffer solution ( Figure S12).
The UV-vis spectra of T1 and T2 complexes in PBS showed, in both cases, the main band relative to the thymine chromophore almost overlapped to that of DAP(T)-OH, further confirming that the nucleobase does not participate to the Pt coordination. This band, having a high extinction molar coefficient, probably submerged possible absorption bands relative to metal/ligands charge-transfer transitions. Indeed, only a weak band at about 330 nm, which proved the presence of the metal in the complexes, was detected ( Figure 2).  The stability of the complexes was evaluated by monitoring their UV spectra in PBS over time for 48 h. In the first hour of monitoring, an increase in both the 268 and 330 nm bands occurred with a concomitant 1 nm red-shift of the maximum of the 268-nm band (Figures S13a and S14a). Then, after 1 h, the weak metal-to-ligand charge transfer (MLCT) band started to decrease, probably due to the exchange reactions between water and the labile ligands. The overall UV signal stabilized after 48 h (Figures S13b and S14b).
Overall, the variations in the UV-vis spectra of both metal complexes were barely detectable, resulting in a slight hyperchromic-and red-shift of the band at 268 nm and a small decrease in the 330 nm band (Figures S13c and S14c).

NMR Analysis of T1 and T2 Platinum Complexes in Aqueous Solution
Since only moderate changes were detected in the UV-vis spectra of T1 and T2 in aqueous solution during the time-course experiments, due to the strong absorption of the nucleobase with respect to the weak MLCT bands of the metal complexes, we followed their stability over time using another technique. In particular, by using 1 H-NMR experiments, we observed that both the platinum complexes were stable for months in DMSO-d6. By adding 10% D2O to the DMSO-d6 solution of T1 and T2, we evidenced the appearance of new signals and the intensity reduction of others, denoting that more than one species was formed from the original ones. However, with only 10% water, the complexes were still quite stable. Indeed, the new species started appearing after 8 h, and intact T1 and T2 were still present in the solution for almost 50% of their initial amount after 48 h (see Figure  S15a for T2). Probably, the first exchanged ligand by water was chloride, followed (after at least 24 h) by DMSO, as evidenced by the appearance of the free DMSO signal (at 2.23 ppm). The hydrolysis of the Pt complexes was also monitored by dissolving them directly in D2O. Obviously, in this case, the process was faster, affording the complete exchange of the DMSO ligand after 48 h, and the detachment from the metal also of the DAP(T)-OH ligand after 96 h (see Figure S15b for T2 complex). Even if monitoring T1 was complicated by the presence of the rotamers, which rendered the spectra interpretation more difficult, by following the appearance of the free DMSO signal in both the complexes dissolved in D2O, we observed a slightly faster exchange of this ligand for T2 than for T1 ( Figure S16). The stability of the complexes was evaluated by monitoring their UV spectra in PBS over time for 48 h. In the first hour of monitoring, an increase in both the 268 and 330 nm bands occurred with a concomitant 1 nm red-shift of the maximum of the 268-nm band (Figures S13a and S14a). Then, after 1 h, the weak metal-to-ligand charge transfer (MLCT) band started to decrease, probably due to the exchange reactions between water and the labile ligands. The overall UV signal stabilized after 48 h (Figures S13b and S14b).
Overall, the variations in the UV-vis spectra of both metal complexes were barely detectable, resulting in a slight hyperchromic-and red-shift of the band at 268 nm and a small decrease in the 330 nm band (Figures S13c and S14c).

NMR Analysis of T1 and T2 Platinum Complexes in Aqueous Solution
Since only moderate changes were detected in the UV-vis spectra of T1 and T2 in aqueous solution during the time-course experiments, due to the strong absorption of the nucleobase with respect to the weak MLCT bands of the metal complexes, we followed their stability over time using another technique. In particular, by using 1 H-NMR experiments, we observed that both the platinum complexes were stable for months in DMSO-d 6 . By adding 10% D 2 O to the DMSO-d 6 solution of T1 and T2, we evidenced the appearance of new signals and the intensity reduction of others, denoting that more than one species was formed from the original ones. However, with only 10% water, the complexes were still quite stable. Indeed, the new species started appearing after 8 h, and intact T1 and T2 were still present in the solution for almost 50% of their initial amount after 48 h (see Figure S15a for T2). Probably, the first exchanged ligand by water was chloride, followed (after at least 24 h) by DMSO, as evidenced by the appearance of the free DMSO signal (at 2.23 ppm). The hydrolysis of the Pt complexes was also monitored by dissolving them directly in D 2 O. Obviously, in this case, the process was faster, affording the complete exchange of the DMSO ligand after 48 h, and the detachment from the metal also of the DAP(T)-OH ligand after 96 h (see Figure S15b for T2 complex). Even if monitoring T1 behavior was complicated by the presence of the rotamers, which rendered the spectra interpretation more difficult, by following the appearance of the free DMSO signal in both the complexes dissolved in D 2 O, we observed a slightly faster exchange of this ligand for T2 than for T1 ( Figure S16).

Antiproliferative Activity of the T1 and T2 Platinum Complexes
The antiproliferative effects of T1 and T2 complexes were evaluated on three different tumor cell lines (i.e., HeLa, human cervical adenocarcinoma; WM266, metastatic melanoma; MCF-7, breast adenocarcinoma) and one healthy cellular model (HDF, human fibroblasts). Cells were treated with only with the vehicle) for each compound is reported in Figure 3.
The results indicated that the complexes showed a good antiproliferative activity on HeLa cells with a cell viability reduction of 23% and 29%, at 25 μM, and 55% and 54% at 50 μM, respectively, for T1 and T2. The target complexes were less active on WM266 and MCF-7 cells, reducing their viability by about 20% at the highest tested concentration (50 μM). In turn, the free ligand DAP(T)-OH did not affect the proliferation of all the tested cells, indicating that the activity found for T1 and T2 is essentially due to the presence of platinum.
However, T1 and T2 complexes proved to be less active than cisplatin (used as positive control) on the treated tumor cells, but, remarkably, more selective with respect to the healthy ones ( Figure  S17). In fact, T1 and T2 did not interfere with the HDF proliferation at the tested concentrations ( Figure 3).

CD-Monitored Binding Experiments of the New Platinum Complexes with DNA Model Systems
Subsequently, the novel Pt(II) complexes T1 and T2, as well as the nucleoamino acid DAP(T)-OH, were studied by CD spectroscopy in their interaction in solution with DNA sequences representing useful model systems [38,39]. In detail, we used a 12-mer random coil single strand (ODN1) containing a central box with two contiguous guanines (GG box), and three secondary structure-forming oligonucleotides (ODNs), i.e., two hairpin duplexes of 12 base-pairs (one with and the other without a central GG box), and a unimolecular G-quadruplex (G4) model with three Gquartets. The hairpin duplexes were formed by two 27-mer self-complementary single strands, classical models for B DNA duplexes (ds27: two tracts of the Dickerson sequence joined by a central three-thymine (TTT) loop [40,41]; and dsGG: two 12-mer tracts, one of which contained a GG box, joined by a central TTT loop), whereas the unimolecular G4 was derived from the 26-mer human telomere sequence (tel26), which can form in proper conditions G-quadruplex structures. The strong interest for G-quadruplexes is due to the formation of these non-canonical DNA structures in some The results indicated that the complexes showed a good antiproliferative activity on HeLa cells with a cell viability reduction of 23% and 29%, at 25 µM, and 55% and 54% at 50 µM, respectively, for T1 and T2. The target complexes were less active on WM266 and MCF-7 cells, reducing their viability by about 20% at the highest concentration tested (50 µM). In turn, the free ligand DAP(T)-OH did not affect the proliferation of all the tested cells, indicating that the activity found for T1 and T2 is essentially due to the presence of platinum.
However, T1 and T2 complexes proved to be less active than cisplatin (used as positive control) on the treated tumor cells, but, remarkably, more selective with respect to the healthy ones ( Figure S17). In fact, T1 and T2 did not interfere with the HDF proliferation at the tested concentrations ( Figure 3).

CD-Monitored Binding Experiments of the New Platinum Complexes with DNA Model Systems
Subsequently, the novel Pt(II) complexes T1 and T2, as well as the nucleoamino acid DAP(T)-OH, were studied by CD spectroscopy in their interaction in solution with DNA sequences representing useful model systems [38,39]. In detail, we used a 12-mer random coil single strand (ODN1) containing a central box with two contiguous guanines (GG box), and three secondary structure-forming oligonucleotides (ODNs), i.e., two hairpin duplexes of 12 base-pairs (one with and the other without a central GG box), and a unimolecular G-quadruplex (G4) model with three G-quartets. The hairpin duplexes were formed by two 27-mer self-complementary single strands, classical models for B DNA duplexes (ds27: two tracts of the Dickerson sequence joined by a central three-thymine (TTT) loop [40,41]; and dsGG: two 12-mer tracts, one of which contained a GG box, joined by a central TTT loop), whereas the unimolecular G4 was derived from the 26-mer human telomere sequence (tel 26 ), which can form in proper conditions G-quadruplex structures. The strong interest for G-quadruplexes is due to the formation of these non-canonical DNA structures in some regions of the human genome, especially in telomeres and in regulatory regions of some oncogenes [42][43][44].
All the CD-binding experiments were performed in a K + -rich buffered solution (100 mM KCl, 7 mM Na 2 HPO 4 /NaH 2 PO 4 , pH = 7.2) to mimic the intracellular physiological conditions. The ODNs used as DNA model systems were subjected to the annealing procedure taking the sequences in the selected buffer at high temperature (95 • C) for 5 min, and then leaving them to slowly cool to room Pharmaceuticals 2020, 13, 284 9 of 20 temperature. This procedure allows structuring either the duplexes and G4 structures, as verified by the CD spectra ( Figure S18). The conformation adopted by tel 26 after annealing in the selected buffer was essentially a hybrid-2 type structure, as evidenced by the comparison of its CD spectrum in Figure  S18d with those reported in the literature [45,46].
Since the contribution to the CD signal of the starting nucleoamino acid and the Pt complexes was negligible at the concentration used for the experiments (Figure S19), we monitored the CD profiles of the ODN systems before and after incubation with the target molecules (10 equiv.) dissolved in DMSO, at different time periods (0, 2, 24, and 48 h) after the addition. As a reference, we also monitored upon time the CD signal of the ODN solutions after the addition of pure DMSO (same volume as the one added in previous incubations with the compounds) without evidencing significant changes in the overall CD spectra.
As shown in Figure 4a,b, significant changes in the CD spectrum of ODN1 were observed when this was treated with T1 and T2, evidencing that both complexes interacted with this single strand oligonucleotide. In contrast, the starting nucleoamino acid did not produce relevant CD variations on ODN1 (Figure 4c). In detail, in the presence of T1, the CD spectrum of ODN1 showed a decrease over time of the band at 275 nm accompanied by a red-shift of the band maximum reaching the highest effects 48 h after the complex addition (∆CD 275 = 1.3 mdeg, 5 nm red-shift). More marked changes in the CD band were observed when complex T2 was added to the ODN1 solution. Upon time, the CD spectrum exhibited a dramatic decrease in the CD signal at 275 nm (ca 70%) accompanied by a 10 nm red-shift of the band maximum.
regions of the human genome, especially in telomeres and in regulatory regions of some oncogenes [42][43][44].
All the CD-binding experiments were performed in a K + -rich buffered solution (100 mM KCl, 7 mM Na2HPO4/NaH2PO4, pH = 7.2) to mimic the intracellular physiological conditions. The ODNs used as DNA model systems were subjected to the annealing procedure taking the sequences in the selected buffer at high temperature (95 °C) for 5 min, and then leaving them to slowly cool to room temperature. This procedure allows structuring either the duplexes and G4 structures, as verified by the CD spectra ( Figure S18). The conformation adopted by tel26 after annealing in the selected buffer was essentially a hybrid-2 type structure, as evidenced by the comparison of its CD spectrum in Figure S18d with those reported in the literature [45,46].
Since the contribution to the CD signal of the starting nucleoamino acid and the Pt complexes was negligible at the concentration used for the experiments (Figure S19), we monitored the CD profiles of the ODN systems before and after incubation with the target molecules (10 equiv.) dissolved in DMSO, at different time periods (0, 2, 24, and 48 h) after the addition. As a reference, we also monitored upon time the CD signal of the ODN solutions after the addition of pure DMSO (same volume as the one added in previous incubations with the compounds) without evidencing significant changes in the overall CD spectra.
As shown in Figure 4a,b, significant changes in the CD spectrum of ODN1 were observed when this was treated with T1 and T2, evidencing that both complexes interacted with this single strand oligonucleotide. In contrast, the starting nucleoamino acid did not produce relevant CD variations on ODN1 (Figure 4c). In detail, in the presence of T1, the CD spectrum of ODN1 showed a decrease over time of the band at 275 nm accompanied by a red-shift of the band maximum reaching the highest effects 48 h after the complex addition (ΔCD275 = 1.3 mdeg, 5 nm red-shift). More marked changes in the CD band were observed when complex T2 was added to the ODN1 solution. Upon time, the CD spectrum exhibited a dramatic decrease in the CD signal at 275 nm (c.a. 70%) accompanied by a 10 nm red-shift of the band maximum.  Similarly to ODN1, CD spectroscopy was used to evaluate the interaction of T1, T2, and DAP(T)-OH with the selected duplex DNA models. In these cases, small changes in the CD spectra of the duplexes were observed when T1 and T2 were added to the oligonucleotide Pharmaceuticals 2020, 13, 284 10 of 20 solutions ( Figure S20a,b,e,f), whereas no changes were recorded for the incubation with DAP(T)-OH ( Figure S20c,g). In particular, with both the duplex systems, a reduction in the CD signal of about 1 mdeg was observed after incubation with T1 ( Figure S20a,d for ds27, and Figure S20e,h for dsGG). T2 also produced a red-shift of the band maximum of the duplexes of ca. 2 nm, along with a CD intensity decrease, which, however, was more pronounced for the duplex containing the GG box compared to ds27 ( Figure S20b,d for ds27 and Figure S20f,h for dsGG).
As far as the interactions with the G4 was concerned, only slight differences between the CD spectrum of tel 26 in the absence and presence of the nucleoamino acid DAP(T)-OH were observed up to 48 h (Figure 5c). In contrast, after the addition of T1 or T2 to the G4 solution, both the main band at 290 nm and the shoulder at 267 nm significantly decreased over time, reaching, also in this case, the maximum effects after 48 h incubation (Figure 5a,b). added compound. The experiments were carried out in 100 mM KCl, 7 mM Na2HPO4/NaH2PO4, pH = 7.2, at 20 °C (optical path = 1 cm).
Similarly to ODN1, CD spectroscopy was used to evaluate the interaction of T1, T2, and DAP(T)-OH with the selected duplex DNA models. In these cases, small changes in the CD spectra of the duplexes were observed when T1 and T2 were added to the oligonucleotide solutions ( Figure  S20a,b,ef), whereas no changes were recorded for the incubation with DAP(T)-OH ( Figure S20c,g). In particular, with both the duplex systems, a reduction in the CD signal of about 1 mdeg was observed after incubation with T1 ( Figure S20a,d for ds27, and S20e,h for dsGG). T2 also produced a red-shift of the band maximum of the duplexes of ca. 2 nm, along with a CD intensity decrease, which, however, was more pronounced for the duplex containing the GG box compared to ds27 ( Figure  S20b,d for ds27 and S20f,h for dsGG).
As far as the interactions with the G4 was concerned, only slight differences between the CD spectrum of tel26 in the absence and presence of the nucleoamino acid DAP(T)-OH were observed up to 48 h (Figure 5c). In contrast, after the addition of T1 or T2 to the G4 solution, both the main band at 290 nm and the shoulder at 267 nm significantly decreased over time, reaching, also in this case, the maximum effects after 48 h incubation (Figure 5a,b). Taken together, the CD data suggested that DNA can be a possible target of the newly obtained compounds, similar to other well-known anticancer Pt complexes [6,7,12,21,23,47,48], with the DAP(T)-based Pt complexes inducing important conformational changes in G4 structures and single stranded ODNs upon binding contrarily to the duplex structure (either containing or not the GG box).
To compare the ability of the complexes to bind the different DNA systems with that of cisplatin, the same CD experiments performed with T1 and T2 were also carried out with CDDP under identical experimental conditions. In agreement with our previous work [47], CDDP proved to Taken together, the CD data suggested that DNA can be a possible target of the newly obtained compounds, similar to other well-known anticancer Pt complexes [6,7,12,21,23,47,48], with the DAP(T)-based Pt complexes inducing important conformational changes in G4 structures and single stranded ODNs upon binding, contrarily to the duplex structure (either containing or not the GG box).
To compare the ability of the complexes to bind the different DNA systems with that of cisplatin, the same CD experiments performed with T1 and T2 were also carried out with CDDP under identical experimental conditions. In agreement with our previous work [47], CDDP proved to significantly interact with the random-coil single strand containing a GG box (ODN1, Figure S21a) and the GG-containing duplex (dsGG, Figure S21c), whereas it was not able to perturb or disrupt the compact G4 structure of tel 26 (Figure S21d) nor the duplex not-containing the GG box ( Figure S21b). Furthermore, while CDDP evidenced a clear selectivity towards duplex structures containing a GG box Pharmaceuticals 2020, 13, 284 11 of 20 (dsGG vs. ds27, Figure S21b,c), T1 and T2 did not efficiently interact with duplex structures, either containing or not a GG-box element ( Figure S20b,c).
Finally, since the UV bands of T1, T2, and DAP(T)-OH significantly overlapped with those of the selected ODN systems, contrarily to CD analysis, UV data were not useful to interpret the binding behavior of these complexes towards different DNA structures.

PAGE-Monitored Binding Experiments of the New Platinum Complexes with DNA Model Systems
The structured DNA model systems that had evidenced, from the CD studies, the higher conformational variations upon binding with the Pt complexes, were selected for native polyacrylamide gel electrophoresis (PAGE) experiments to obtain qualitative data on DNA platination and compare the behavior of T1 and T2 with that of CDDP. In particular, the G4 tel 26 and the duplex containing the GG box (dsGG) were incubated separately for 48 h with 10 equiv. of T1, T2, and CDDP at room temperature. Inspection of the gel, reported in Figure 6a, evidenced that DNA platination on the GG-duplex occurred efficiently by CDDP, as expected, and to a less extent by T1 and T2 (with T2 > T1), whereas the G4 tel 26 was platinated more by T1 and T2 (T2 > T1) than by CDDP (Figure 6b). Thus, PAGE data were in perfect agreement with the CD results ( Figure S20e,f, Figure 5a,b, and Figure S21c,d).
Furthermore, while CDDP evidenced a clear selectivity towards duplex structures containing a GG box (dsGG vs. ds27, Figure S21b,c), T1 and T2 did not efficiently interact with duplex structures, either containing or not a GG-box element (Figure S20b,c).
Finally, since the UV bands of T1, T2, and DAP(T)-OH significantly overlapped with those of the selected ODN systems, contrarily to CD analysis, UV data were not useful to interpret the binding behavior of these complexes towards different DNA structures.

PAGE-Monitored Binding Experiments of the New Platinum Complexes with DNA Model Systems
The structured DNA model systems that had evidenced, from the CD studies, the higher conformational variations upon binding with the Pt complexes, were selected for native polyacrylamide gel electrophoresis (PAGE) experiments to obtain qualitative data on DNA platination and compare the behavior of T1 and T2 with that of CDDP. In particular, the G4 tel26 and the duplex containing the GG box (dsGG) were incubated separately for 48 h with 10 equiv. of T1, T2, and CDDP at room temperature. Inspection of the gel, reported in Figure 6a, evidenced that DNA platination on the GG-duplex occurred efficiently by CDDP, as expected, and to a less extent by T1 and T2 (with T2 > T1), whereas the G4 tel26 was platinated more by T1 and T2 (T2 > T1) than by CDDP (Figure 6b). Thus, PAGE data were in perfect agreement with the CD results ( Figure S20e,f, Figure 5a,b, and Figure S21c,d).
To exclude the contribution of DMSO in the appearance of additional, smeared DNA bands after ligand incubation, the oligonucleotides were also treated in the same conditions with equal amounts of this solvent without the ligands. In these experiments, no difference with the reference DNA bands was evidenced, demonstrating that the observed effects were not due to the solvent ( Figure S22).  To exclude the contribution of DMSO in the appearance of additional, smeared DNA bands after ligand incubation, the oligonucleotides were also treated in the same conditions with equal amounts of this solvent without the ligands. In these experiments, no difference with the reference DNA bands was evidenced, demonstrating that the observed effects were not due to the solvent ( Figure S22).

Reagents, Instruments, and General Methods
All the reagents and solvents were of the highest commercially available quality and were used as received. The coupling reactions were performed under an argon atmosphere, and all the reagents were previously co-evaporated with anhydrous CH 3 CN. Thin layer chromatography (TLC) analyses were carried out on silica gel plates from Macherey-Nagel (60, F254). Reaction products on TLC plates were visualized by 254 nm UV-light. DNA sequences were provided by Biomers.net GmbH (Ulm, Germany).
NMR spectra were recorded on Bruker Avance III HD 400 MHz and Varian Inova 500 MHz NMR spectrometers, as specified. All the chemical shifts (δ) in 1 H-and 13 C-NMR spectra are expressed in ppm with respect to the residual solvent (CHD 2 SOCD 3 , DMSO-d 5 , δ = 2.50 ppm, quintet) or tetramethylsilane (TMS) signals. All the coupling constants (J) are quoted in Hertz (Hz). The following abbreviations were used to explain the multiplicities: s = singlet; d = doublet; t = triplet; q = quartet; quin = quintet; m = multiplet; b = broad.
MALDI-TOF mass spectrometric analyses were performed on a TOF/TOF™ 5800 System in a positive mode, using 2,5-dihydroxybenzoic acid (DHB) or α-cyano-4-hydroxycinnamic acid (CHCA) as the matrices. For the deposition on the MALDI plate, the droplet spotting method was used. The sample (1 mg/mL in CH 3 CN/CH 3 OH or CH 3 CN/H 2 O, 7:3, v/v) was first deposited on the plate (0.5 µL) followed by matrix deposition (10 mg/mL in the same solvent mixture of the sample) and properly mixed before drying the components.
LC-ESI-MS analyses were performed on an Agilent 6230B TOF LC/MS instrument, equipped with a 1260 Infinity HPLC analytical system with binary pump coupled with a 6230 time of flight mass spectrometer as a detector and an Electrospray source; an Agilent ZORBAX C18 column (1.8 µm, 50 × 4.6 mm) for reverse-phase liquid chromatography were used. Stock solutions of the samples were prepared at 2 mg/mL concentration in HPLC grade CH 3 CN/H 2 O. The injections were carried out at a final concentration of 4 ng/µL in CH 3 CN/H 2 O, using a flow rate of 0.4 mL/min. Column elution was performed using H 2 O (A) (with or without 0.05% TFA, as specified) and CH 3 CN (B) as eluents. An isocratic elution of B in A for 3 min was followed by a gradient elution increasing B over 10 min. The ESI/TOF-MS was operated in positive ion mode (100-1500 m/z values).
The semipreparative purifications were carried out on a Hewlett Packard/Agilent 1100 series HPLC system, equipped with a UV detector, using a Phenomenex Luna C18 100 Å (5 µm, 4.6 × 150 mm) column. Gradient elution was carried out at 25 • C (monitoring at 254 nm) by using a gradient that started with buffer A (0.05% TFA in water) and applying buffer B (0.05% TFA in acetonitrile) with a flow rate of 1 mL min −1 .
Samples were lyophilized in an FD4 Freeze Dryer (Heto Lab Equipment) for 16 h. UV-vis measurements were performed on a JASCO V-550 UV-vis spectrophotometer equipped with Peltier Thermostat JASCO ETC-505T.
CD spectra were recorded with a Jasco J-715 spectropolarimeter equipped with a Peltier-type temperature control system (model PTC-348WI).

Platination Reaction of DAP(T)-OH
The nucleoamino acid derivative DAP(T)-OH (4, 25 mg, 0.092 mmol) was suspended in CH 3 OH (1.35 mL). In parallel, K 2 PtCl 4 (1 equiv., 10.58 mg, 0.092 mmol) was dissolved in the minimum amount of H 2 O (150 µL). In 1 h, the amino acid solution was slowly added to the aqueous solution of K 2 PtCl 4 (final solvents ratio: CH 3 OH/H 2 O, 9:1, v/v). The reaction mixture was kept under stirring in the dark and at room temperature for 6 h until the formation of an almost clear yellow solution from the initial dark orange one, with the concomitant disappearance of the DAP(T)-OH white suspension. Subsequently, the solvent was removed under vacuum at 30 • C, and the reaction crude was dried for 1 h at the oil pump to remove traces of H 2 O. Then, the crude mixture was sequentially resuspended after sonication in various solvents (dichloromethane, chloroform, and acetone) and centrifuged, affording, in all cases, a dark-yellow precipitate and a colorless supernatant. This solution, analyzed by TLC, did not show UV-vis bands and was consequently discarded. In contrast, treatment of the precipitate with CH 3 OH gave a pale-yellow solution and a dark-yellow precipitate. Thus, a series of centrifugations and washings of the precipitate with CH 3 OH (until the supernatant was completely colorless) was performed, and the combined yellow methanol solutions (ca. 6 × 5 mL) were taken to dryness. Then, the dark-yellow solid was resuspended by sonication with H 2 O obtaining a yellow supernatant and a white precipitate. After centrifugations and washings of the precipitate with H 2 O (until the supernatant was completely colorless), the aqueous solutions (ca. 3 × 5 mL) were combined, and immediately frozen and lyophilized to remove water from the complex. The white precipitate was then discarded, and the two obtained yellow components (yellow powders) were separately analyzed. LC-ESI-MS analysis of the two Pt complexes was performed as follows: the complexes were dissolved in H 2 O/CH 3 CN (9:1, v/v), injected on a C18 column, and eluted in gradient mode (3 min isocratic elution with 5% CH 3 CN in H 2 O, then gradient to 50% CH 3 CN in 10 min; t R = 0.94 and 0.89 min, for methanol-and water-recovered Pt complexes, respectively; see Figure S4a).
Since the most common NMR organic solvents (CDCl 3 , CD 3 OD, CD 3 COCD 3 ) did not solubilize the recovered Pt complexes at a proper concentration for a complete NMR characterization, we used DMSO for their solubilization. The newly obtained DAP(T)-based complexes were named T1 and T2 (originated from the DMSO-exchange reaction of the Pt complex recovered in CH 3 OH and H 2 O, respectively). The purity of the obtained complexes was checked by LC-ESI-MS, which evidenced the presence of a single peak for each compound ( Figure S5a). For the LC-ESI-MS characterization, T1 and T2 were dissolved in H 2 O/CH 3 CN (9:1, v/v), injected on a C18 column, and eluted as follows: 3 min isocratic elution with 10% CH 3 CN in H 2 O, then gradient to 95% CH 3 CN in 10 min (t R = 0.94 and 0.84 min, for T1 and T2, respectively). Several attempts to obtain also MALDI-TOF spectra of the two complexes were performed using CHCA and DHB as matrixes and various laser powers, obtaining, in all cases, many adducts with the matrix and degradation products.
Based on their chemical structures (as deduced by NMR and mass data), the synthesis yields of T1 and T2 from the complexation reaction of DAP(T)-OH with K 2 PtCl 4 followed by DMSO-exchange, were 35 and 23%, respectively.
Attempts to obtain crystals of the initial complexes, as well as of T1 and T2, suitable for X-ray crystallography, failed, giving only degradation products (white crystals).

Cell Proliferation Experiments
Cells were plated at a density of 1200 cells/well for HeLa, 2000 for WM266, MCF-7, and HDF in 96-well microplates (Corning) and incubated at 37 • C. After 24 h, cells were treated for 48 h with the compounds previously solubilized. In detail, the Pt complexes and DAP(T)-OH were dissolved in DMSO at a 10 mM concentration, while cisplatin was solubilized in an aqueous solution of DMSO (10%)/NaCl (0.9%), at a 2 mM concentration [50], then diluted with growth medium until the final solution contained no more than 0.5% DMSO, well-tolerated by in vitro cell cultures. Cell proliferation was determined by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay (MTT, Sigma Aldrich, Milano, Italy) after 48 h incubation [51]. Plates were then analyzed using a microplate reader (Enspire, Perkin Elmer, Waltham, MA, USA) at 570 nm. The results are reported as the percentage of living cells with respect to the control (vehicle-treated cells) and are expressed as means ± SE of at least three independent experiments performed in triplicate.

UV-Vis Experiments
The UV spectra were recorded using a scanning speed of 100 nm/min and a 2.0 nm bandwidth with the appropriate baseline subtraction. A quartz cuvette with a path length of 1 cm was used (3.5 mL internal volume). The UV-vis spectra of the compounds were recorded in PBS (137 mM NaCl, 2.7 mM KCl, 10 mM Na 2 HPO 4 , 1.8 mM KH 2 PO 4 ) over time in the range of 220 to 450 nm to study their stability. The solutions analyzed were 80 µM in PBS and were obtained after dilution from the original stock solution (7 mM in DMSO).

CD Experiments
The CD spectra were recorded at 20 • C in a quartz cuvette with a path-length of 1 cm using the following parameters: spectral window 240-320 nm, response 1 s, scanning speed 100 nm/min, bandwidth 2.0 nm. All the spectra were averaged over 3 scans and corrected by subtraction of the background scan with buffer. For all the experiments, oligonucleotides were dissolved at 2 µM concentration, stock solutions of ligands [T1, T2, and DAP(T)-OH] were prepared at 7 mM conc. in DMSO, whereas stock CDDP solution was obtained at a 7 mM concentration in an aqueous solution of DMSO (10%)/NaCl (0.9%) [50]. A buffer solution of 7 mM Na 2 HPO 4 /NaH 2 PO 4 , 100 mM KCl (pH 7.2) was used for the studies on the interaction between the DNA model systems and the platinum-based complexes.

PAGE Experiments
Annealed oligonucleotides samples, dissolved at 2 µM concentration in 7 mM Na 2 HPO 4 /NaH 2 PO 4 , 100 mM KCl (pH 7.2) were incubated with 10 equiv. of each platinum complex. After 48 h incubation at room temperature (r.t.), the samples, including the reference DNA, were loaded on 25% polyacrylamide gels in TBE 1× as running buffer. All the mixtures were supplemented with 5% glycerol just before loading and then run, under native conditions, at 80 V at r.t. for 3.3 h. Gels were stained with a GelGreen solution (supplemented with 0.1 M NaCl) for 30 min and finally visualized with a UV transilluminator (BioRad ChemiDoc XRS, Milano, Italy). Each experiment was performed in duplicate.

Conclusions
In this work, the nucleoamino acid DAP(T)-OH, derived by the coupling of l-2,3-diaminopropanoic acid with a thymine acetic acid, was synthesized and characterized via mass spectrometry and NMR spectroscopy and used for the reaction with a platinum(II) salt to obtain novel Pt(II) complexes. Two new platinum-based complexes, named T1 and T2, were obtained and characterized by various techniques. These compounds include in their structures one nucleoamino acid unit [DAP(T)-OH], a platinum(II) ion, a chloride ion, and a DMSO molecule. The identity of the new metal complexes was ascertained by NMR spectroscopy ( 1 H and 13 C, COSY, HSQC, HMBC, and NOESY experiments) and mass spectrometry (LC-ESI-MS) techniques.
The cytotoxicity of T1 and T2, as well as of DAP(T)-OH used as a reference, was tested, in preliminary assays, on a panel of human cancer (HeLa, WM266, MCF-7) and normal (HDF) cells using the MTT assay. CDDP was also tested as a positive control. Both the Pt complexes showed good antiproliferative activity on HeLa cells. Indeed, T1 and T2 at 50 µM concentration reduced HeLa cell viability more than 50% after 48 h incubation, whereas, at the same tested concentration, they were less active on WM266 and MCF-7, suggesting a selectivity of action towards the specific tumor cells that is an important feature in cancer therapy. It is worth noting that, although T1 and T2 complexes resulted less effective in blocking cell proliferation than cisplatin, they were more selective towards cancer cells than healthy ones, as demonstrated by comparing the activity on HeLa cells with that observed on HDF ones, on which the complexes were essentially inactive even at the highest concentration tested. Interestingly, the free ligand DAP(T)-OH did not affect all the tested cells indicating that the observed bioactivity is essentially driven by the presence of the platinum center.
We also hypothesized that the nucleobase could contribute to the bioactivity of the Pt complexes by both protecting the Pt center from premature deactivation and increasing the cellular uptake of the complexes, plausibly thanks to specific nucleobase transporters, thus giving a synergistic effect together with the presence of the metal. Furthermore, generally, single nucleobases do not show relevant biological activity (nor significantly interact with DNA). In addition, as previously reported [21], the Pt complex with DAP-OH as ligand did not evidence significant antiproliferative activity in the same experimental conditions, showing a 50% inhibition of HeLa cells proliferation only at 220 µM concentration, whereas T1 and T2 seemed to be about 4-times more active on the same cancer cells.
Once the antiproliferative effects of the platinum-based complexes were assessed, to explore if their activity could be correlated with their DNA-binding ability, T1 and T2, as well as DAP(T)-OH and cisplatin, used as reference compounds, were studied using CD spectroscopy. Their interaction in solution was investigated with four DNA model systems, i.e., a random coil single strand, two B form-duplexes, one with and the other without a GG box, and a G-quadruplex structure. From CD binding experiments, it emerged that DNA can be a possible target of these brand new compounds, similar to other reported bioactive Pt complexes (as well as transition metal complexes, such as ruthenium complexes) [6,7,12,15,21,23,47,48,52,53]. In particular, we observed significant changes only in the CD spectrum of the single strand and G4 when T1 and T2 were added to each DNA system, evidencing that both the complexes interacted with these oligonucleotides. A more marked interaction seemed to occur in the case of T2 with respect to T1. On the contrary, the interaction of the starting nucleoamino acid with all the tested DNA systems was almost null, in line with the absence of specific antiproliferative effects observed in cell assays. Thus, CD data were in agreement with the observed biological activity for all the compounds. Furthermore, comparing the DNA-binding behavior of the new Pt complexes with that of cisplatin, it emerged that, while CDDP efficiently interacted with duplex structures containing a GG box not being able to perturb or disrupt the compact structure of the G4, T1 and T2 resulted good G4-binders as revealed by both CD-and PAGE-monitored binding experiments.
The moderate cytotoxicity combined with the selectivity of the Pt(II) complexes obtained and described in the present work, can be of pharmaceutical interest in multiple drug therapy. In addition, the synthesis and characterization of DAP-based nucleoamino acids also containing the other nucleobases, i.e., DAP(C)-OH, DAP(A)-OH, and DAP(G)-OH, are ongoing in our laboratories to use these nucleamino acid scaffolds as building blocks for the preparation of novel Pt complexes endowed with increased activity and selectivity, identifying the most promising analogs of the series.  interaction seemed to occur in the case of T2 with respect to T1. On the contrary, the interaction of the starting nucleoamino acid with all the tested DNA systems was almost null, in line with the absence of specific antiproliferative effects observed in cell assays. Thus, CD data were in agreement with the observed biological activity for all the compounds. Furthermore, comparing the DNAbinding behavior of the new Pt complexes with that of cisplatin, it emerged that, while CDDP efficiently interacted with duplex structures containing a GG box not being able to perturb or disrupt the compact structure of the G4, T1 and T2 resulted good G4-binders as revealed by both CD-and PAGE-monitored binding experiments. The moderate cytotoxicity combined with the selectivity of the Pt(II) complexes obtained and described in the present work, can be of pharmaceutical interest in multiple drug therapy. In addition, the synthesis and characterization of DAP-based nucleoamino acids also containing the other nucleobases, i.e., DAP(C)-OH, DAP(A)-OH, and DAP(G)-OH, are ongoing in our laboratories to use these nucleamino acid scaffolds as building blocks for the preparation of novel Pt complexes endowed with increased activity and selectivity, identifying the most promising analogs of the series.