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The Coordination Abilities of Three Novel Analogues of Saliva Peptides: The Influence of Structural Modification on the Copper Binding

  • Aleksandra Kotynia
  • Edward Krzyżak
  • Elżbieta Kamysz
  • Małgorzata Sobocińska
  • Justyna BrasuńEmail author
Open Access
Article
  • 1.5k Downloads

Abstract

Three novel analogues of salivary peptides as sialorphin (QHNPR) and opiorphin (QRFSR) were synthesized by the solid-phase method. The sequences of these ligands were following: AHNPR, QANPR and QRFPR. The aim of our work was investigation in what way some structural modifications may impact on coordination abilities of studied peptides. In this work we presented the interaction of pentapeptides with copper(II) ions in wide range of pH. To determine the coordination model of ligands there were carried out several studies by spectroscopy (UV–Vis, CD) methods and potentiometric measurements.

Keywords

Analogues of salivary pentapeptides Stability constants of copper(II) complexes Peptide synthesis UV–Vis and CD spectroscopy 

Introduction

Human opiorphin (QRFSR) and rat sialorphin (QHNPR) are natural inhibitors of enkephalin catabolism. Opiorphin was identified in human saliva and it showed beneficial effects in pain management, antidepressant-like actions as well as in involvement in colonic motility and erectile physiology (Davies 2009; Thanawala et al. 2008; Tian et al. 2009; Tong et al. 2008; Wisner et al. 2006; Yang et al. 2011). Sialorphin is a peptide synthesized predominantly in the submandibular gland and prostate of adult rats in response to androgen steroids, and is released locally and systemically in response to stress (Rougeot et al. 2003). Sialorphin exhibits a potent analgesic activity and plays a crucial role in the control of social behavior, pain perception and in sexual behavior (Davies et al. 2007; Messaoudi et al. 2004; Rougeot et al. 2003).

The metal ions such as Cu(II), Ni(II), and Zn(II) are essential and beneficial elements in mammalian nutrition, are required in a number of enzymatic reactions and can be important regulators of activity of many peptides (Barnea 1989; Cummins and O’Connor 1998; Gerega et al. 1988).

Copper ions play an important role in the progression of neurodegenerative diseases (Migliorini et al. 2014; Valensin et al. 2016), affect the development and progression of different cancers (Khanna et al. 2013), exhibit anti-inflammatory effects (Lewis 1984), are essential for bone integrity and elasticity (Sierpinska et al. 2014), influence tooth demineralization and remineralization (Abdullah et al. 2006; Brookes et al. 2003) as well as aroma perception by affecting volatility of aroma compounds in the mouth through interaction with salivary components, especially proteins (Hong et al. 2006). Human body is provided in various complicated mechanisms involving interactions with proteins and other molecules that make copper available during its deficiency, as well as enable elimination of excessive copper through absorption, transport, distribution, storage and excretion. Any failure of the copper homeostasis results inevitably in severe diseases. Elevated levels of salivary copper are observed in patients with oral submucous fibrosis, oral leukoplakia and oral cancer (Ayinampudi and Narsimhan 2012; Trivedy et al. 1999, 2000, 2001). The copper deficiency is associated with a decreased bone strength and deterioration of bone quality leading to osteoporotic defects (Medeiros et al. 1997).

In this study, we present the synthesis of some analogues of sialorphin to investigate in what way some structural modification may have an impact on coordination abilities of the peptides. We present the interaction of new pentapeptides with Cu(II) ions over a wide pH range. To determine the coordination model of ligands, a series of measurements using the spectroscopic (UV–Vis, CD) and potentiometric techniques has been performed.

Experimental

Peptide Synthesis and Purification

All of the peptides were synthesized on a solid-phase method using standard Fmoc procedures on a 2-chlorotrityl chloride resin (loading 0.3–0.9 mmol/g, 1% DVB, 200–400 mesh, Orpegen Peptide Chemicals GmbH, Heideberg, Germany). N-α-protected amino acids, and reagents used for the solid-phase synthesis were obtained from Iris Biotech GmbH (Marktredwitz, Germany). Peptides chains were elongated in the consecutive cycles of deprotection and coupling. Two deprotection steps using 20% piperidine in dimethylformamide (DMF) (5 and 15 min) were performed. The coupling reactions were carried out with a threefold molar excess of the protected amino acid (Fmoc-AA) dissolved in DMF/dichloromethane (DCM) using N,N′-diisopropylcarbodiimide (DIC) and N-hydroxybenzotriazole (HOBt) for 2 h (Fmoc-AA:HOBt:DIC, 1:1:1). The completeness of each coupling step was monitored by the chloranil test. The peptides were cleaved from the resin and the protecting groups were removed in one step using a mixture of TFA/triisopropylsilane/H2O (95:2.5:2.5, v/v/v). The cleaved peptides were precipitated with cold diethyl ether and lyophilized.

The peptides were purified using the RP-HPLC on a Kromasil C8 column (8 × 250 mm, 100 Å pore size, 5 µm particle size) with linear gradient 2–40% of acetonitrile in 0.1% TFA for 30 min with a flow rate of 10 mL/min. The purity of the peptides was checked on a Beckman HPLC controlled by Lp-Chrom system. Fractions containing the pure peptides (>98%) were pooled and lyophilized. The mass spectrometry analysis were carried out on a MALDI-TOF MS. Physicochemical characteristics of all synthesized peptides are presented in Table 1.

Table 1

Physicochemical characteristics of investigated peptides

Peptide

Sequence

Formula

HPLC Rt (min)

[M]+ calc .

[M + H]+ found

Opiorphin

QRFSR

C29H48N12O8

6.7a

692.4

693.3

Sialorphin

QHNPR

C26H42N12O8

5.5a

650.3

651.2

P1

QRFPR

C31H50N12O7

7.87b

702.4

703.1

P2

AHNPR

C24H39N11O7

5.37b

593.29

594.8

P3

QANPR

C23H40N10O8

5.21b

584.29

585.0

aLinear gradient from 2 to 40% of [B] in [A] for 15 min, flow rate of 1.5 mL/min, Kromasil C8 column (5 μm, 4.6 × 250 mm), where [A] is 0.1% TFA in H2O and [B] is 0.1% TFA in acetonitrile

bLinear gradient from 2 to 60% of [B] in [A] for 15 min, flow rate of 1.5 mL/min, Kromasil C8 column (5 μm, 4.6 × 250 mm), where [A] is 0.1% TFA in H2O and [B] is 0.1% TFA in acetonitrile

Potentiometry Measurements

The potentiometry titrations were conducted on a MOLSPIN pH-meter system, using a Mettler Toledo InLab®Micro combined electrode. The pH-meter system was calibrated by triple titration of hydrogen ion (HCl) before each measurement. The potentiometric experiments were performed in argon atmosphere over the pH range 3.0–11.5 at 298 K. The ligands were dissolved in HCl/KCl where pH = 3.0 and I = 0.1 M (KCl), the ligands concentration were 1 × 10−3 M. The accurate concentration of ligands solutions were determined by Gran method. The samples of each titration were prepared by adding equimolar amounts of CuCl2 solutions. Titration volume were 1–1.5 ml and alkali (c(KOH) ~0.1 M) was added from a 0.250 ml micrometer syringe. The stability constants for the proton (βi (H)) and Cu(II) complexes (β(CupHqLr)) were calculated by HYPERQUAD 2008 (written by Peter Gans, Protonic Software) and SUPERQUAD computer programs (Gans et al. 1985, 1996). The protonation constants of ligands is determined by: βi = [HiL]/[H+]i[L] and the equilibrium of complex stability: βpqr = [MpHqLr]/[M]p[H]q[L]r. Standard deviations were computed by these both programs and refer to random errors only.

Spectroscopy Measurements (UV–Vis, CD)

All spectroscopic measurements were carried out at 298 K. The solutions of samples were prepared in similar way like samples used in pH-metric titration. The pH of the samples were determined by adding small quantity of concentrated solutions of KOH. The UV–Vis absorption spectra of complexes were recorded on Varian Carry 50 Bio spectrophotometer. All spectra were collected in quartz cells with 1 cm path length and spectral range was 230–800 nm. For each spectra were calculated the molar extinction coefficients [ε (M−1 cm−1)] at a wavelength of maximum absorption. The circular dichroism (CD) spectra were recorded on a magnetic circular spectrometer JASCO J-1500. The measurements were conducted in 0.5 cm cuvettes in the range 240–800 nm with 0.1 nm resolution. The measurements were carried out in an inert gas atmosphere (N2). The CD spectral data were recalculated to the molar ellipticity [ε (M−1 cm−1)].

Results and Discussion

The presented manuscript shows the binding abilities of three novel analogues of saliva pentapeptides: opiorphin and sialorphin (Scheme 1a, b). The characteristic feature of these ligands is the presence the glutamate amino acid residue in the position 1 of the peptide chain. Moreover sialorphin has His and Pro moieties located at position 2 and 4 of the peptide chain (Scheme 1b). These two residues significantly influence the process of the metal ion binding (Kozłowski et al. 1999; Pettit et al. 1985; Sovago and Osz 2006; Sovago et al. 2016).

Scheme 1

The full protonated structure of: a opiorphin, b sialorphin, and their analogues: c P1–QRFPR, d P2–AHNPR, e P3–QANPR

The modification of the opiorphin has been performed by the insertion of proline residue instead of the serine located at position 4 (P1, Scheme 1c). Next two analogues have been created by the insertion of alanine residue instead of Gln-1 (P2, Scheme 1d) or His-2 (P3, Scheme 1e) in the sialorphin sequence. The detailed analysis of the results obtained for these analogues in comparison to the results for the parent peptide allows to characterize the influence of the specific amino acid resides as Gln, His, Pro or Asn on the coordination abilities of two selected saliva peptides.

The first step of the presented studies is the analysis of the results obtained for the analogue of opiorphin (P1). The acid-base properties as well as the stabilities constants of formed complexes and the spectral abilities are presented in Table 2.

Table 2

Protonation constants of P1–QRFPR and stability constants with the spectroscopic parameters for its Cu(II) complexes at T = 293 K, I = 0.1 M (KCl)

P1

Species

logβ

pK

HL

11.34 ± 0.04

11.34 (Arg)

H2L

18.42 ± 0.05

7.08 (-NH2)

H3L

21.53 ± 0.05

3.11 (-COO)

Cu(II) complexes

Species/binding model

logβ

pK

UV–Vis

CD

λ(nm)

ε(M−1 cm−1)

λ(nm)

ε(M−1 cm−1)

CuHL {NH2, 3H2O}

16.42 ± 0.08

 

680

47

315

0.25

CuL {NH2, N am, 2H2O}

10.71 ± 0.04

7.33

640

89

566

−0.41

    

315

0.89

    

268

−1.22

CuH−1L {NH2, 2N am, H2O}

3.87 ± 0.05

9.39

573

138

569

−0.85

    

315

1.02

    

275

−1.03

CuH−2L {NH2, 2N am, OH}

−5.64 ± 0.07

11.14

573

134

562

−0.85

    

315

0.97

    

270

−1.75

CuH− 3L {NH2, 2N am, OH}

−17.03 ± 0.11

 

579

112

545

−0.80

    

315

0.63

    

270

−3.43

The ligand P1 forms five types of complexes as its parent peptide (Fig. 1a; Table 1). The metal ion binding by P1 starts around pH 4 by the formation of the CuHL species, which achieves its highest concentration at pH 5.5 (Fig. 1a). The value of logβ * = 5.08, were logβ * = logβ CuHL  − logβ HL , is comparable to stabilities calculated for the complexes with the N terminal amino group involved in Cu(II) binding (Prenesti et al. 1999). Moreover, the λmax for d-d transition at 680 nm confirms the involvement only one nitrogen donor in metal ion binding (Prenesti et al. 2006).

Fig. 1

a The species distribution curve of formed Cu(II) complexes in dependence on pH for P1 (solid line) and opiorphin (dashed line). b The diagram for competitive binding of Cu(II) ions by P1 (solid line) and opiorphin (dashed line) ligands. The opiorphin:Cu(II):P1 molar ratio is 1:1:1, C = 1 × 10−3M

Afterwards, with the increase of pH, the involvement of the first and the second amide takes place and formation of the species with the {NH2, N am, 2×H2O}, {NH2, 2×N am, H2O} (Scheme 2) donor atoms in the plane is observed, consecutively. The location of the λmax for d–d transitions at CuL640 nm and CuH−1L573 nm are in good agreement with the theoretical λmax = 650, 576 nm calculated for proposed donor sets (Billo 1974; Prenesti et al. 1999). Moreover, the involvement of the N terminal amino as well as amide donors in Cu(II) coordination is supported by presence of one negative and one positive CT bands at 270 and 320 nm (Table 2), consecutively. Up to pH 7, the process of Cu(II) binding by the unmodified and modified opiorphin is carried out in the same manner. Nevertheless, the insertion of proline in position 4 promotes the formation of the species with {NH2, 2xN am, H2O} coordination. Above last to complexes appear in the investigated system: CuH−2L and CuH−3L, and this process does not influences significantly the spectral abilities of the system (Table 2).

Scheme 2

The schematic structures of the Cu(II) complexes existing in the salivary range of pH (6.5–7.5) in the system with ligands P1, P2 and P3. The water molecules were omitted to more clarity

As it was mentioned above in the case of opiorphin the formation next two species is observed at significantly lower range of pH. Moreover the unmodified opiorphin, involves third amide donor in Cu(II) binding and forms the species with the {NH2, 3xN am} binding manner (Kotynia et al. 2010). This ability is associated with the absence of the Pro-4 in the peptide backbone. The proline is the amino acid residue which strongly influences the binding ability of the peptide. When proline is present in the peptide chain starting from the position 2, it effectively prevents binding of the subsequent amide donors (Bataille et al. 1984; Formicka-Kozlowska et al. 1981; Kozłowski et al. 1999). Owing to this fact and any significant changes in the spectral abilities of the system above pH 9,5, the formation of the CuH−2L and CuH−3L complexes may be assigned to proton dissociation form the metal bound water molecule(Holm et al. 1996; Jakab et al. 2008; Kamysz et al. 2013) and guanidyl group of the side chain of arginine moiety (Fitch et al. 2015; Holm et al. 1996; Matera et al. 2008).

As it was mentioned, the insertion of the proline in the fourth position of the peptide backbone effectively prevents the involvement of the subsequent amide donor, however due to this fact, the system with the ligand P1 is more specific and selective in comparison to the unmodified opiorphin.

The investigations of the coordination abilities of two new analogues of sialorphin: P2 and P3 (Scheme 1 d, e) were the next step of our studies. The modification in the case of the first sialorphin analogue (P2) consisted in the replacement of Gln-1 by alanine moiety and it does not influences the binding abilities of P2. It forms the same type of dominant complexes as unmodified ligand (Kamysz et al. 2013). The species CuL dominating at physiological range of pH is the characteristic complex for His-2 peptides (Kozłowski et al. 1999) with three nitrogen donors from: N terminal amino group, first amide and imidazole ring for His-2 moiety (Scheme 2). The presence of these donors in the coordination sphere of Cu(II) ion is supported by the CT transitions at: 340 and 263 nm (Table 3) in CD spectrum. Moreover the location of the d–d band at 600 nm (Table 3) is almost the same as theoretical λmax = 599 nm, calculated for the –NH2, N am, NIm, H2O chromophores, what supports the postulated coordination mode. The appearance of the final species significantly influences the spectral abilities as the red shift of the λmax d–d 600 nm → 528 nm what suggests four nitrogen donors in the square plane symmetry (Casolaro et al. 1999; Marchewka et al. 2002). The formation such complex is possible when: the N terminal amino group, two amides and amide form the side chain if Asn-3 are bound to Cu(II). The same type of the species was found for the sialorphin (Kamysz et al. 2013).

Table 3

Protonation constants of peptides P2–AHNPR and P3–QANPR and stability constants with the spectroscopic parameters for Cu(II) complexes at T = 298 K, I = 0.1 M (KCl)

P2

Species

logβ

pK

HL

∼11.91 ± 0.09

∼11.91 (Arg)

H2L

19.83 ± 0.09

7.92 (–NH2)

H3L

26.01 ± 0.10

6.19 (NIm)

H4L

29.11 ± 0.10

3.10 (–COO)

Cu(II) complexes

Species/binding model

logβ

pK

UV–Vis

CD

λ (nm)

ε (M−1 cm−1)

λ (nm)

ε (M−1 cm−1)

CuH2L {NH2, 3H2O}

25.22 ± 0.04

 

CuL {NH2, N am, Nim, H2O}

17.89 ± 0.01

7.33

600

68

607

0.37

    

511

−0.07

    

340

0.26

    

263

2.35

CuH−1L {NH2, 2N am, Nim}

8.50 ± 0.02

9.39

575

66

585

0.33

    

480

−0.07

    

320

0.28

    

260

2.44

CuH−2L {NH2, 2N am, NH Asn3}

−2.64 ± 0.03

11.14

528

85

618

0.10

    

504

0.13

    

309

0.70

    

274

−1.16

P3

Species

logβ

pK

HL

∼11.19 ± 0.04

∼11.19 (Arg)

H2L

18.62 ± 0.05

7.43 (–NH2)

H3L

21.98 ± 0.06

3.36 (–COO)

Cu(II) complexes

Species/binding model

logβ

pK

UV–Vis

CD

λ (nm)

ε (M−1 cm−1)

λ (nm)

ε (M−1 cm−1)

CuHL {NH2, 3H2O}

16.74 ± 0.03

 

678

15

CuH−1L {NH2, 2N am, H2O}

5.78 ± 0.02

10.96

550

98

590

−0.37

    

500

0.19

    

311

0.65

    

276

−1.43

    

243

1.90

CuH−2L {NH2, 2N am, OH}

−2.96 ± 0.03

8.74

544

95

580

−0.37

    

493

0.19

    

310

0.61

    

274

−1.57

    

243

1.50

CuH−3L {NH2, 2N am, NH Asn3}

−12.83 ± 0.03

9.87

520

81

562

−0.50

    

493

0.34

    

305

0.80

    

268

−2.10

As it was presented above, the modification does not influences significantly the binding abilities of the peptide however the efficiency in Cu(II) binding changes (Fig. 2). Below pH 8, the P2 is around 20% less effective in Cu(II) binding however its efficiency significantly increases above this pH. It is probably caused by the steric changes induced less developed side chain of alanine than glutamine.

Fig. 2

The diagram for competitive binding of Cu(II) ions by P2 and sialorphin. The sialorphin:Cu(II):P1 molar ratio is 1:1:1, Cl = 1 × 10−3M

The interesting results have been obtained for the third from investigated peptide P3 (Scheme 1e) consisting alanine in position 2 instead of His moiety. Moreover, due to the presence of Pro-4 residue in the peptide chain it can be also assigned as the analogue of P1. The comparison of the coordination abilities between P3 and P1 and sialorphin, shows that P3 has higher similarity in copper coordination as P1 than sialorphin.

P3 starts Cu(II) binding by formation of the CuHL species with metal ion anchored by the N terminal amino group (Fig. 3a), as it was found in a case of P1. Then with increase of pH simultaneous dissociation of two protons take place and the CuH−1L appears in the system. This process is correlated with the involvement of the next two nitrogen donors binding to copper ion, what is confirmed by the spectroscopic results obtained for the CuH−1L species (Table 3, Scheme 2).

Fig. 3

a The species distribution curve of formed Cu(II) complexes in dependence on pH for P3 (solid line) and P1 (dashed line). b The diagram for competitive binding of Cu(II) ions by P3 (solid line) and P1 (dashed line) ligands. The P3:Cu(II):P1 molar ratio is 1:1:1, C = 1 × 10−3M

The presence of CT transitions at 311, 276 and 243 nm (Table 3) in CD spectrum confirm the involvement of the amido and amino donors in copper (II) binding. Moreover, the location of d–d supports involvement of three nitrogen donors in copper binding. Owing to these facts, the discussed complex can be characterized by the {NH2, 2×N am, H2O} binding mode and it dominates in salivary range of pH as in a case of P1 (Scheme 2).

With increase of pH last two species exist in the system. First of them is the CuH−2L, which achieves its highest concentration at pH 9.5 (Fig. 3a). The spectroscopic parameters of the system at pH 9.5 do not change significantly (Table 3) what may support the proton dissociation form the metal bound water molecule (Holm et al. 1996; Jakab et al. 2008; Kamysz et al. 2013). The spectral abilities of the investigated system dramatically change above pH 10, in which the dominant is the CuH−3L species. The most of all the shift of λmax to 520 nm (Table 3) strongly support the involvement of the fourth nitrogen in copper binding and formation of the complex with square planar symmetry.

Based on the peptide structure and the previous results for sialorphin (Kamysz et al. 2013), there is only one possibility to involve fourth nitrogen in Cu(II) coordination: it is the amide nitrogen from the side chain of Asn-3 residue (Scheme 3). The same process was also observed in a case of P2 (Scheme 3) as well as unmodified sialorphin (Kamysz et al. 2013).

Scheme 3

The schematic structures of the final Cu(II) complexes existing in basic pH in the system with ligands P1, P2 and P3

Despite the fact, that both peptides form the same type of dominant complexes, except the last one, they show different efficiency in metal binding (Fig. 3b). Starting already from pH 5 the P3 is getting to be significantly more effective in copper binding as the P2. This difference may be caused by the fact that the P3 has alanine residue at position 2 of the peptide backbone. Alanine is the amino acid with simpler side chain in comparison to arginine, which is present in the second position of the P1 peptide chain and the simultaneously involvement of two amide donors and formation of the more stable species with the {NH2, 2N am} is observed already at pH 5 in contrast to P1 (Fig. 3a).

Conclusions

In the presented manuscript we have characterized coordination abilities of new analogues of the saliva peptides (opiorphin and sialorhin) toward Cu(II) ions. The detailed analysis of the results obtained for these analogues in comparison to the results for the parent peptides allowed to characterize the influence of the specific amino acid resides as Gln, His, Pro or Asn on the coordination abilities of two selected saliva peptides as well as the efficiency in metal binding. The knowledge on coordination abilities of salivary peptides and their analogues by copper ions is crucial for a rational drug design of new therapeutic agents that could be involved in the regulation of the level of copper ions.

Notes

Acknowledgements

The presented solution studies were financially supported by Wroclaw Medical University ST.D080.16.006.

Compliance with Ethical Standards

Conflict of interest

All Authors declare that they have no conflict of interest.

Ethical Approval

This article does not contain any studies with human participants or animals performed by any of the authors.

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© The Author(s) 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Aleksandra Kotynia
    • 1
  • Edward Krzyżak
    • 1
  • Elżbieta Kamysz
    • 2
  • Małgorzata Sobocińska
    • 2
  • Justyna Brasuń
    • 1
    Email author
  1. 1.Department of Inorganic ChemistryWroclaw Medical UniversityWroclawPoland
  2. 2.Laboratory of Chemistry of Biological Macromolecules, Department of Molecular Biotechnology, Faculty of ChemistryUniversity of Gdansk80-308 GdańskPoland

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