Repozytorium

The Role of the Unbinding Cycle on the Coordination Abilities of the Bi-Cyclopeptides toward Cu(II) Ions

Autorzy

Alicja Lisowska

Paulina Świątek

Filip Dębicki

Agnieszka Lewińska

Aleksandra Marciniak

Lorenzo Pacini

Anna Maria Papini

Justyna Brasuń

Rok wydania

2024

Czasopismo

Molecules

Numer woluminu

29

Strony

2197/1-2197/12

DOI

10.3390/molecules29102197

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Bicyclic peptides have attracted the interest of pharmaceutical companies because of their remarkable properties, putting them on a new path in medicine. Their conformational rigidity improves proteolytic stability and leads to rapid penetration into tissues via any possible route of administration. Moreover, elimination of renal metabolism is of great importance, for example, for people with a history of liver diseases. In addition, each ring can function independently, making bicyclic peptides extremely versatile molecules for further optimization. In this paper, we compared the potentiometric and spectroscopic properties studied by UV–vis, MCD, and EPR of four synthetic analogues of the bi-cyclic peptide c(PKKHP-c(CFWKTC)-PKKH) (BCL). In particular, we correlated the structural and spectral properties of complexes with coordinating abilities toward Cu(II) ions of MCL1 (Ac-PKKHPc(CFWKTC)PKKH-NH2 ) that contains the unbinding cycle and N- and C-terminal linear parts with two histidine residues, one per part; two monocyclic ligands containing one histidine residue, both in the N-terminal position, i.e., MCL2 (Ac-PKKHPc(CFWKTC)PKKS-NH2 ) and in the C-terminal position, i.e., MCL3 (Ac-PKKSPc(CFWKTC)PKKH-NH2 ), respectively; and the linear structure LNL (Ac-PKKHPSFWKTSPKKH-NH2 ). Potentiometric results have shown that the bicyclic structure promotes the involvement of the side chain imidazole donors in Cu(II) binding. On the other hand, the results obtained for the mono-cyclic analogues lead to the conclusion that the coordination of the histidine moiety as an anchoring group is promoted by its location in the peptide sequence further from the nonbinding cycle, strongly influencing the involvement of the amide donors in Cu(II) coordination.

Słowa kluczowe

bi-cyclopeptide, histidine, metal complex, copper ions, stability constant, spectroscopic studies

Licencja otwartego dostępu

CC-BY

Licencja na prawach której można swobodnie kopiować, rozprowadzać, zmieniać i remiksować objęty prawem autorskim utwór (Utwór-przedmiot prawa autorskiego) pod warunkiem podania imienia i nazwiska autora utworu pierwotnego oraz źródła pochodzenia utworu.

Pełny tekst licencji: https://creativecommons.org/licenses/by/3.0/pl/legalcode

Adres publiczny

http://dx.doi.org/10.3390/molecules29102197

Strona internetowa wydawcy

http://www.mdpi.com/journal/metals

Podobne publikacje
2011

Copper(II) complexation by (pyridinyl)aminomethane-1,1-diphosphonic acid derivatives; spectroscopic and potentiometric studies.

Kowalik-Jankowska Teresa, Pietruszka Marta M., Jezierska Julia, Matczak-Jon Ewa, Kafarski Paweł

2014

Structural aspects of copper(II) binding by a multi-His analogue of somatostatin.

Marciniak Aleksandra, Czyżnikowska Żaneta, Cebrat Marek, Kotynia Aleksandra, Brasuń Justyna

2005