Identification of Plakortide E from the Caribbean Sponge Plakortis halichondroides as a Trypanocidal Protease Inhibitor using Bioactivity-Guided Fractionation

Autor: Oli, Swarna, Abdelmohsen, Usama Ramadan, Hentschel, Ute, Schirmeister, Tanja
Rok vydání: 2014
Předmět:
Proteases
Stereochemistry
medicine.medical_treatment
Trypanosoma brucei brucei
Plakortis halichondroides
Pharmaceutical Science
Trypanosoma brucei
01 natural sciences
570 Life sciences
Dioxanes
protease inhibitor
03 medical and health sciences
ddc:593
Drug Discovery
medicine
Animals
Humans
Protease Inhibitors
cathepsin
lcsh:QH301-705.5
Pharmacology
Toxicology and Pharmaceutics (miscellaneous)

IC50
030304 developmental biology
Trypanocidal agent
rhodesain
chemistry.chemical_classification
0303 health sciences
Protease
Antiparasitic Agents
biology
010405 organic chemistry
Communication
plakortide E
biology.organism_classification
Cathepsins
Trypanocidal Agents
Antiparasitic agent
Protease inhibitor (biology)
Porifera
0104 chemical sciences
Cysteine Endopeptidases
slowly-binding reversible inhibitor
Enzyme
lcsh:Biology (General)
Biochemistry
chemistry
Drug Screening Assays
Antitumor

570 Biowissenschaften
medicine.drug
Zdroj: Marine Drugs, 12 (5). pp. 2614-2622.
Marine Drugs, Vol 12, Iss 5, Pp 2614-2622 (2014)
Marine Drugs
Popis: In this paper, we report new protease inhibitory activity of plakortide E towards cathepsins and cathepsin-like parasitic proteases. We further report on its anti-parasitic activity against Trypanosoma brucei with an IC50 value of 5 mu M and without cytotoxic effects against J774.1 macrophages at 100 mu M concentration. Plakortide E was isolated from the sponge Plakortis halichondroides using enzyme assay-guided fractionation and identified by NMR spectroscopy and mass spectrometry. Furthermore, enzyme kinetic studies confirmed plakortide E as a non-competitive, slowly-binding, reversible inhibitor of rhodesain.
Databáze: OpenAIRE