Cyclic Dipeptides: The Biological and Structural Landscape with Special Focus on the Anti-Cancer Proline-Based Scaffold.

cyclic dipeptides diketopiperazines drug discovery privileged scaffold proline-based DKPs supramolecular structuring

Journal

Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414

Informations de publication

Date de publication:
14 10 2021
Historique:
received: 18 09 2021
revised: 11 10 2021
accepted: 12 10 2021
entrez: 23 10 2021
pubmed: 24 10 2021
medline: 20 1 2022
Statut: epublish

Résumé

Cyclic dipeptides, also know as diketopiperazines (DKP), the simplest cyclic forms of peptides widespread in nature, are unsurpassed in their structural and bio-functional diversity. DKPs, especially those containing proline, due to their unique features such as, inter alia, extra-rigid conformation, high resistance to enzyme degradation, increased cell permeability, and expandable ability to bind a diverse of targets with better affinity, have emerged in the last years as biologically pre-validated platforms for the drug discovery. Recent advances have revealed their enormous potential in the development of next-generation theranostics, smart delivery systems, and biomaterials. Here, we present an updated review on the biological and structural profile of these appealing biomolecules, with a particular emphasis on those with anticancer properties, since cancers are the main cause of death all over the world. Additionally, we provide a consideration on supramolecular structuring and synthons, based on the proline-based DKP privileged scaffold, for inspiration in the design of compound libraries in search of ideal ligands, innovative self-assembled nanomaterials, and bio-functional architectures.

Identifiants

pubmed: 34680148
pii: biom11101515
doi: 10.3390/biom11101515
pmc: PMC8533947
pii:
doi:

Substances chimiques

Diketopiperazines 0
Dipeptides 0
Peptides, Cyclic 0
Proline 9DLQ4CIU6V

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Joanna Bojarska (J)

Faculty of Chemistry, Institute of General & Inorganic Chemistry, Technical University of Lodz, 90-924 Lodz, Poland.

Adam Mieczkowski (A)

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland.

Zyta M Ziora (ZM)

Institute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD 4072, Australia.

Mariusz Skwarczynski (M)

School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.

Istvan Toth (I)

Institute for Molecular Bioscience, The University of Queensland, St. Lucia, QLD 4072, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.
School of Pharmacy, The University of Queensland, Woolloongabba, QLD 4102, Australia.

Ahmed O Shalash (AO)

School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.

Keykavous Parang (K)

Center for Targeted Drug Delivery, Department of Biomedical and Pharmaceutical Sciences, Harry and Diane Rinker Health Science Campus, School of Pharmacy, Chapman University, Irvine, CA 92618, USA.

Shaima A El-Mowafi (SA)

Center for Targeted Drug Delivery, Department of Biomedical and Pharmaceutical Sciences, Harry and Diane Rinker Health Science Campus, School of Pharmacy, Chapman University, Irvine, CA 92618, USA.

Eman H M Mohammed (EHM)

Center for Targeted Drug Delivery, Department of Biomedical and Pharmaceutical Sciences, Harry and Diane Rinker Health Science Campus, School of Pharmacy, Chapman University, Irvine, CA 92618, USA.

Sherif Elnagdy (S)

Botany Department, Faculty of Science, Cairo University, Giza 12613, Egypt.

Maha AlKhazindar (M)

Botany Department, Faculty of Science, Cairo University, Giza 12613, Egypt.

Wojciech M Wolf (WM)

Faculty of Chemistry, Institute of General & Inorganic Chemistry, Technical University of Lodz, 90-924 Lodz, Poland.

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