Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling

Aggregation of amyloid-β peptides (Aβ) is a hallmark of Alzheimer’s disease (AD), which is affecting an increasing number of people. Hence, there is an urgent need to develop new pharmaceutical treatments which could be used to prevent the AD symptomatology. Activity-dependent neuroprotective protei...

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Main Authors: Ancuta-Veronica Lupaescu, Cosmin Stefan Mocanu, Gabi Drochioiu, Catalina-Ionica Ciobanu
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/14/10/1011
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author Ancuta-Veronica Lupaescu
Cosmin Stefan Mocanu
Gabi Drochioiu
Catalina-Ionica Ciobanu
author_facet Ancuta-Veronica Lupaescu
Cosmin Stefan Mocanu
Gabi Drochioiu
Catalina-Ionica Ciobanu
author_sort Ancuta-Veronica Lupaescu
collection DOAJ
description Aggregation of amyloid-β peptides (Aβ) is a hallmark of Alzheimer’s disease (AD), which is affecting an increasing number of people. Hence, there is an urgent need to develop new pharmaceutical treatments which could be used to prevent the AD symptomatology. Activity-dependent neuroprotective protein (ADNP) was found to be deficient in AD, whereas NAP, an 8-amino-acid peptide (<sup>1</sup>NAPVSIPQ<sup>8</sup>) derived from ADNP, was shown to enhance cognitive function. The higher tendency of zinc ion to induce Aβ aggregation and formation of amorphous aggregates is also well-known in the scientific literature. Although zinc binding to Aβ peptides was extensively investigated, there is a shortage of knowledge regarding the relationship between NAP peptide and zinc ions. Therefore, here, we investigated the binding of zinc ions to the native NAP peptide and its analog obtained by replacing the serine residue in the NAP sequence with tyrosine (<sup>1</sup>NAPVYIPQ<sup>8</sup>) at various molar ratios and pH values by mass spectrometry (MS) and nuclear magnetic resonancespectroscopy (NMR). Matrix-assisted laser desorption/ionization time-of-flight (MALDI ToF) mass spectrometry confirmed the binding of zinc ions to NAP peptides, while the chemical shift of Asp<sup>1</sup>, observed in <sup>1</sup>H-NMR spectra, provided direct evidence for the coordinating role of zinc in the N-terminal region. In addition, molecular modeling has also contributed largely to our understanding of Zn binding to NAP peptides.
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spelling doaj.art-f647a269b531470daeae6a615b3cc3c12023-11-22T19:36:02ZengMDPI AGPharmaceuticals1424-82472021-10-011410101110.3390/ph14101011Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular ModelingAncuta-Veronica Lupaescu0Cosmin Stefan Mocanu1Gabi Drochioiu2Catalina-Ionica Ciobanu3Integrated Center for Research, Development and Innovation in Advanced Materials, Nanotechnologies and Distributed Systems for Fabrication and Control (MANSiD), Stefan cel Mare University of Suceava, 720229 Suceava, RomaniaFaculty of Chemistry, Alexandru Ioan Cuza University, 11 Carol I, 700506 Iasi, RomaniaFaculty of Chemistry, Alexandru Ioan Cuza University, 11 Carol I, 700506 Iasi, RomaniaCERNESIM Centre, Institute of Interdisciplinary Research, Alexandru Ioan Cuza University of Iasi, 11 Carol I, 700506 Iasi, RomaniaAggregation of amyloid-β peptides (Aβ) is a hallmark of Alzheimer’s disease (AD), which is affecting an increasing number of people. Hence, there is an urgent need to develop new pharmaceutical treatments which could be used to prevent the AD symptomatology. Activity-dependent neuroprotective protein (ADNP) was found to be deficient in AD, whereas NAP, an 8-amino-acid peptide (<sup>1</sup>NAPVSIPQ<sup>8</sup>) derived from ADNP, was shown to enhance cognitive function. The higher tendency of zinc ion to induce Aβ aggregation and formation of amorphous aggregates is also well-known in the scientific literature. Although zinc binding to Aβ peptides was extensively investigated, there is a shortage of knowledge regarding the relationship between NAP peptide and zinc ions. Therefore, here, we investigated the binding of zinc ions to the native NAP peptide and its analog obtained by replacing the serine residue in the NAP sequence with tyrosine (<sup>1</sup>NAPVYIPQ<sup>8</sup>) at various molar ratios and pH values by mass spectrometry (MS) and nuclear magnetic resonancespectroscopy (NMR). Matrix-assisted laser desorption/ionization time-of-flight (MALDI ToF) mass spectrometry confirmed the binding of zinc ions to NAP peptides, while the chemical shift of Asp<sup>1</sup>, observed in <sup>1</sup>H-NMR spectra, provided direct evidence for the coordinating role of zinc in the N-terminal region. In addition, molecular modeling has also contributed largely to our understanding of Zn binding to NAP peptides.https://www.mdpi.com/1424-8247/14/10/1011NMR spectroscopyNAP-type peptidesneuroprotectionzinc bindingmolecular modelingAlzheimer’s disease
spellingShingle Ancuta-Veronica Lupaescu
Cosmin Stefan Mocanu
Gabi Drochioiu
Catalina-Ionica Ciobanu
Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling
Pharmaceuticals
NMR spectroscopy
NAP-type peptides
neuroprotection
zinc binding
molecular modeling
Alzheimer’s disease
title Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling
title_full Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling
title_fullStr Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling
title_full_unstemmed Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling
title_short Zinc Binding to NAP-Type Neuroprotective Peptides: Nuclear Magnetic Resonance Studies and Molecular Modeling
title_sort zinc binding to nap type neuroprotective peptides nuclear magnetic resonance studies and molecular modeling
topic NMR spectroscopy
NAP-type peptides
neuroprotection
zinc binding
molecular modeling
Alzheimer’s disease
url https://www.mdpi.com/1424-8247/14/10/1011
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AT gabidrochioiu zincbindingtonaptypeneuroprotectivepeptidesnuclearmagneticresonancestudiesandmolecularmodeling
AT catalinaionicaciobanu zincbindingtonaptypeneuroprotectivepeptidesnuclearmagneticresonancestudiesandmolecularmodeling