Use of Optogenetic Amyloid-β to Monitor Protein Aggregation in

Alzheimer’s Disease Amyloid-β Caenorhabditis elegans Drosophila melanogaster Light-sheet Optogenetics Zebrafish

Journal

Bio-protocol
ISSN: 2331-8325
Titre abrégé: Bio Protoc
Pays: United States
ID NLM: 101635102

Informations de publication

Date de publication:
05 Dec 2020
Historique:
received: 22 06 2020
revised: 20 10 2020
accepted: 22 11 2020
entrez: 4 3 2021
pubmed: 5 3 2021
medline: 5 3 2021
Statut: epublish

Résumé

Alzheimer's Disease (AD) has long been associated with accumulation of extracellular amyloid plaques (Aβ) originating from the Amyloid Precursor Protein. Plaques have, however, been discovered in healthy individuals and not all AD brains show plaques, suggesting that extracellular Aβ aggregates may play a smaller role than anticipated. One limitation to studying Aβ peptide

Identifiants

pubmed: 33659494
doi: 10.21769/BioProtoc.3856
pii: e3856
pmc: PMC7842303
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e3856

Informations de copyright

Copyright © The Authors; exclusive licensee Bio-protocol LLC.

Déclaration de conflit d'intérêts

Competing interestsWe have no conflicts of interest to declare.

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Auteurs

Prameet Kaur (P)

Science Division, Yale-NUS College, Singapore.

Caroline Kibat (C)

Institute of Molecular and Cell Biology (IMCB), Singapore.

Emelyne Teo (E)

Science Division, Yale-NUS College, Singapore.

Jan Gruber (J)

Science Division, Yale-NUS College, Singapore.
Department of Biochemistry, National University of Singapore, Singapore.

Ajay Mathuru (A)

Science Division, Yale-NUS College, Singapore.
Department of Physiology, YLL School of Medicine, National University of Singapore, Singapore.
Institute of Molecular and Cell Biology (IMCB), Singapore.

And Nicholas S Tolwinski (ANS)

Science Division, Yale-NUS College, Singapore.

Classifications MeSH