Evaluation of angiotensin converting enzyme inhibitors by SPR biosensor and theoretical studies.


Journal

Enzyme and microbial technology
ISSN: 1879-0909
Titre abrégé: Enzyme Microb Technol
Pays: United States
ID NLM: 8003761

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 19 09 2017
revised: 13 06 2018
accepted: 19 10 2018
entrez: 7 11 2018
pubmed: 7 11 2018
medline: 23 2 2019
Statut: ppublish

Résumé

Surface plasmon resonance (SPR) biosensor has been utilized for monitoring analyte-ligand interactions in modern drug discovery processes. SPR biosensors measure the change in refractive indexes over the course of analyte molecules' binding to a specific immobilized ligand on sensor chip. This effort highlights a comprehensive SPR study besides enzymatic assay for discovery of new Angiotensin Converting Enzyme (ACE) inhibitors via screening of medicinal plants. At first, five medicinal plants were selected as potential sources for developing new ACE inhibitors through hydrolyzing hippuryl-L-histidyl-L-leucine (HHL) assay. The interaction of selected extracts with immobilized ACE on the sensor chip (500D) confirmed that the Onopordum acanthium L. had the greatest ACE inhibition activity among the set of compounds and its active compound (onopordia) was isolated. SPR biosensor used to evaluate binding affinity of onopordia and ACE. Equilibrium constant (K

Identifiants

pubmed: 30396392
pii: S0141-0229(18)30187-X
doi: 10.1016/j.enzmictec.2018.10.010
pii:
doi:

Substances chimiques

Angiotensin-Converting Enzyme Inhibitors 0
Plant Extracts 0

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117-123

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Hafezeh Salehabadi (H)

Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, 14176-53955, Iran.

Khosro Khajeh (K)

Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, 14115-111, Iran.

Bahareh Dabirmanesh (B)

Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, 14115-111, Iran.

Mahmood Biglar (M)

Drug Design and Development Research Center, The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, 14176-53955, Iran.

Massoud Amanlou (M)

Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, 14176-53955, Iran; Drug Design and Development Research Center, The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, 14176-53955, Iran. Electronic address: amanlou@tums.ac.ir.

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Classifications MeSH