Complex-Forming Properties of the Anti-Inflammatory Sialorphin Derivative Palmitic Acid-Lysine-Lysine-Glutamine-Histidine-Asparagine-Proline-Arginine with Cu(II) Ions in an Aqueous Solution

The present work describes the complexation of the anti-inflammatory sialorphin derivative Pal-Lys-Lys-Gln-His-Asn-Pro-Arg (palmitic acid-lysine-lysine-glutamine-histidine-asparagine-proline-arginine) with Cu(II) ions in an aqueous solution, at a temperature of 25.0 ± 0.1 °C, over the whole pH range. The complexing properties were characterized by potentiometric and UV-Vis spectrophotometric methods. The potentiometric method was used to calculate the logarithms of the overall stability constants (log β) and the values of the stepwise dissociation constants (pKa) of the studied complexes. The percentage of each species formed in an aqueous solution was estimated from the species distribution curve as a function of pH. The absorbance (A) and molar absorption coefficient (ε) values for the Cu(II)-sialorphin derivative system were determined with UV-Vis spectroscopy. Our studies indicate that the sialorphin derivative forms stable complexes with Cu(II) ions, which may lead to future biological and therapeutic applications.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:29

Enthalten in:

Molecules (Basel, Switzerland) - 29(2023), 1 vom: 22. Dez.

Sprache:

Englisch

Beteiligte Personen:

Pająk, Marek [VerfasserIn]
Kamysz, Elżbieta [VerfasserIn]
Sikora, Karol [VerfasserIn]
Fichna, Jakub [VerfasserIn]
Woźniczka, Magdalena [VerfasserIn]

Links:

Volltext

Themen:

0RH81L854J
2V16EO95H1
4QD397987E
7006-34-0
94ZLA3W45F
9DLQ4CIU6V
Amino Acids
Anti-Inflammatory Agents
Arginine
Asparagine
Cu(II) complexes
Glutamine
Histidine
Ions
Journal Article
K3Z4F929H6
Lysine
Palmitic Acid
Palmitic acid
Peptides
Potentiometry
Proline
Protonation constant
Sialorphin
Stability constant
UV-Vis spectroscopy

Anmerkungen:

Date Completed 12.01.2024

Date Revised 12.01.2024

published: Electronic

Citation Status MEDLINE

doi:

10.3390/molecules29010090

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM366932527