Hydroxy-Porphyrin as an Effective, Endogenous Molecular Clamp during Early Stages of Amyloid Fibrillization.


Journal

Chemistry, an Asian journal
ISSN: 1861-471X
Titre abrégé: Chem Asian J
Pays: Germany
ID NLM: 101294643

Informations de publication

Date de publication:
01 Dec 2021
Historique:
received: 16 08 2021
pubmed: 28 9 2021
medline: 16 12 2021
entrez: 27 9 2021
Statut: ppublish

Résumé

Amyloid fibril formation of proteins is of great concern in neurodegenerative disease and can be detrimental to the storage and stability of biologics. Recent evidence suggests that insulin fibril formation reduces the efficacy of type II diabetes management and may lead to several complications. To develop anti-amyloidogenic compounds of endogenous origin, we have utilized the hydrogen bond anchoring, π stacking ability of porphyrin, and investigated its role on the inhibition of insulin amyloid formation. We report that hydroxylation and metal removal from the heme moiety yields an excellent inhibitor of insulin fibril formation. Thioflavin T, tyrosine fluorescence, Circular Dichorism (CD) spectroscopy, Field emission scanning electron microscopy (FESEM) and molecular dynamics (MD) simulation studies suggest that hematoporphyrin (HP) having hydrogen bonding ability on both sides is a superior inhibitor compared to hemin and protoporphyrin (PP). Experiments with hen egg white lysozyme (HEWL) amyloid fibril formation also validated the efficacy of endogenous porphyrin based small molecules. Our results will help to decipher a general therapeutic strategy to counter amyloidogenesis.

Identifiants

pubmed: 34570963
doi: 10.1002/asia.202100965
doi:

Substances chimiques

Amyloid 0
Hypoglycemic Agents 0
Porphyrins 0
Protein Aggregates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3931-3936

Subventions

Organisme : DST-Inspire
ID : IFA13-CH-120, 2014
Organisme : Science and Engineering Research Board (SERB)
ID : ECR/2016/001935
Organisme : DST-Inspire
Organisme : CSIR
Organisme : SERB
ID : CRG/2020/005610
Organisme : SERB
ID : MTR/2019/00786
Organisme : Novo Nordisk Foundation
ID : NNFSA170028392

Informations de copyright

© 2021 Wiley-VCH GmbH.

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Auteurs

Soumav Nath (S)

Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, Nadia, 741246, India.

Priti Roy (P)

Department of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, Nadia, 741246, India.

Raki Mandal (R)

Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, Nadia, 741246, India.

Rajat Roy (R)

Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, Nadia, 741246, India.

Alexander K Buell (AK)

Department of Biotechnology and Biomedicine, Technical University of Denmark DTU, Søltofts Plads, 2800 Kgs., Lyngby, Denmark.

Neelanjana Sengupta (N)

Department of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, Nadia, 741246, India.

Pradip K Tarafdar (PK)

Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, Nadia, 741246, India.

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