Phenylalanine-based fibrillar systems.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
07 Dec 2023
Historique:
medline: 11 12 2023
pubmed: 21 11 2023
entrez: 21 11 2023
Statut: epublish

Résumé

Phenylketonuria (PKU) is an inborn metabolic disorder characterized by excess accumulation of phenylalanine (Phe) and its fibril formation, resulting in progressive intellectual disability. Several research groups have approached from various directions to understand the formation of toxic amyloid fibrils from the essential amino acid Phe. Different parameters like the nature of the solvent, pH, Phe concentration, temperature,

Identifiants

pubmed: 37987167
doi: 10.1039/d3cc04138g
doi:

Substances chimiques

Phenylalanine 47E5O17Y3R
Peptides 0
Amyloid 0
Amino Acids 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

14509-14523

Auteurs

Soumen Kuila (S)

Department of Chemistry, University of North Bengal, Raja Rammohanpur, Siliguri 734013, West Bengal, India. jayanta@nbu.ac.in.

Sukantha Dey (S)

Department of Chemistry, University of North Bengal, Raja Rammohanpur, Siliguri 734013, West Bengal, India. jayanta@nbu.ac.in.

Pijush Singh (P)

Department of Chemistry, University of North Bengal, Raja Rammohanpur, Siliguri 734013, West Bengal, India. jayanta@nbu.ac.in.
Department of Biochemistry and Biophysics, University of Kalyani, Kalyani 741235, West Bengal, India.

Akash Shrivastava (A)

Department of Chemistry, University of North Bengal, Raja Rammohanpur, Siliguri 734013, West Bengal, India. jayanta@nbu.ac.in.

Jayanta Nanda (J)

Department of Chemistry, University of North Bengal, Raja Rammohanpur, Siliguri 734013, West Bengal, India. jayanta@nbu.ac.in.

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Classifications MeSH