Solid-Phase Synthesis and


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
12 Oct 2020
Historique:
received: 16 09 2020
revised: 29 09 2020
accepted: 08 10 2020
entrez: 15 10 2020
pubmed: 16 10 2020
medline: 25 2 2021
Statut: epublish

Résumé

Siderophores are iron-complexing compounds synthesized by bacteria and fungi. They are low molecular weight compounds (500-1500 Daltons) possessing high affinity for iron(III). Since 1970 a large number of siderophores have been characterized, the majority using hydroxamate or catecholate as functional groups. The biosynthesis of siderophores is typically regulated by the iron levels of the environment where the organism is located. Because of their exclusive affinity and specificity for iron(III), natural siderophores and their synthetic derivatives have been exploited in the treatment of human iron-overload diseases, as both diagnostic and therapeutic agents. Here, solid-phase approach for the preparation of hexadentate, peptide-based tricatecholato containing peptides is described. The versatility of the synthetic method allows for the design of a common scaffolding structure whereby diverse ligands can be conjugated. With so many possibilities, a computational approach has been developed which will facilitate the identification of those peptides which are capable of providing a high affinity iron(III) binding site. This study reports an integrated computational/synthetic approach towards a rational development of peptide-based siderophores.

Identifiants

pubmed: 33053658
pii: ijms21207498
doi: 10.3390/ijms21207498
pmc: PMC7593911
pii:
doi:

Substances chimiques

Ferric Compounds 0
Iron Chelating Agents 0
Ligands 0
Siderophores 0
Iron E1UOL152H7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Parkinson's UK
ID : K-1603
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_17164
Pays : United Kingdom

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Auteurs

Ranko Gacesa (R)

Institute of Pharmaceutical Science, King's College London, London SE1 9NH, UK.
Department of Gastroenterology and Hepatology, University of Groningen and University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Department of Genetics, University of Groningen and University Medical Center Groningen, 9713 AV Groningen, The Netherlands.

Andrea A P Tripodi (AAP)

Institute of Pharmaceutical Science, King's College London, London SE1 9NH, UK.

Agostino Cilibrizzi (A)

Institute of Pharmaceutical Science, King's College London, London SE1 9NH, UK.

Antonella Leggio (A)

Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.

Robert Hider (R)

Institute of Pharmaceutical Science, King's College London, London SE1 9NH, UK.

Vincenzo Abbate (V)

Department of Analytical, Environmental and Forensic Sciences, King's College London, London SE1 9NH, UK.

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Classifications MeSH