|ZFIN ID: ZDB-PUB-210305-7|
Use of Optogenetic Amyloid-β to Monitor Protein Aggregation in Drosophila melanogaster, Danio rerio and Caenorhabditis elegans
Kaur, P., Kibat, C., Teo, E., Gruber, J., Mathuru, A., Tolwinski, A.N.S.
|Source:||Bio-protocol 10: e3856 (Journal)|
|Registered Authors:||Kibat, Caroline, Mathuru, Ajay|
|Keywords:||Alzheimer’s Disease, Amyloid-β, Caenorhabditis elegans, Drosophila melanogaster, Light-sheet, Optogenetics, Zebrafish|
|PubMed:||33659494 Full text @ Bio Protoc|
Kaur, P., Kibat, C., Teo, E., Gruber, J., Mathuru, A., Tolwinski, A.N.S. (2020) Use of Optogenetic Amyloid-β to Monitor Protein Aggregation in Drosophila melanogaster, Danio rerio and Caenorhabditis elegans. Bio-protocol. 10:e3856.
ABSTRACTAlzheimer'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 in vivo during disease progression is the inability to induce aggregation in a controlled manner. We developed an optogenetic method to induce Aβ aggregation and tested its biological influence in three model organisms-D. melanogaster, C. elegans and D. rerio. We generated a fluorescently labeled, optogenetic Aβ peptide that oligomerizes rapidly in vivo in the presence of blue light in all organisms. Here, we detail the procedures for expressing this fusion protein in animal models, investigating the effects on the nervous system using time lapse light-sheet microscopy, and performing metabolic assays to measure changes due to intracellular Aβ aggregation. This method, employing optogenetics to study the pathology of AD, allows spatial and temporal control in vivo that cannot be achieved by any other method at present.
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