2021
DOI: 10.1002/btm2.10231
|View full text |Cite
|
Sign up to set email alerts
|

Recent advances in cellular biosensor technology to investigate tau oligomerization

Abstract: Tau is a microtubule binding protein which plays an important role in physiological functions but it is also involved in the pathogenesis of Alzheimer's disease (AD) and related tauopathies. While insoluble and β-sheet containing tau neurofibrillary tangles have been the histopathological hallmark of these diseases, recent studies suggest that soluble tau oligomers, which are formed prior to fibrils, are the primary toxic species. Substantial efforts have been made to generate tau oligomers using purified reco… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
15
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
6
1
1

Relationship

1
7

Authors

Journals

citations
Cited by 14 publications
(15 citation statements)
references
References 133 publications
(440 reference statements)
0
15
0
Order By: Relevance
“…In spite of the evident key role of changes of tau phosphorylation and conformational status, assays monitoring these processes are still scarce (17). The conformational biosensors we developed here faithfully reported the conformational change of tau induced by phosphorylation or by MTs destabilization.…”
Section: Application Of Tau Interaction Biosensors For the Identifica...mentioning
confidence: 76%
See 2 more Smart Citations
“…In spite of the evident key role of changes of tau phosphorylation and conformational status, assays monitoring these processes are still scarce (17). The conformational biosensors we developed here faithfully reported the conformational change of tau induced by phosphorylation or by MTs destabilization.…”
Section: Application Of Tau Interaction Biosensors For the Identifica...mentioning
confidence: 76%
“…The sensibility of our K18(P301L) interaction sensor is outstanding, spanning 4 logs of protein concentration of brain lysates and being able to discriminate between brain lysates from control and transgenic mice in as low as 300 pg of total protein after only 24h of incubation. Compared to existing FRET-based K18 aggregation sensors (14,17,50), the Nluc complementation-based Tau(P301L) and K18(P301L) interaction assays presented here are high-throughput compatible and require no further data integration following plate reading of the bioluminescence signal. We provide "proof-of-principle" evidence of the robustness of both assays and its application in the identification of small molecules able to interfere with tau seeding / self-interaction response, opening novel possibilities for the discovery of new drug candidates for tau-related neurodegenerative diseases.…”
Section: Application Of Tau Interaction Biosensors For the Identifica...mentioning
confidence: 99%
See 1 more Smart Citation
“…Researchers are making a substantial effort to generate tau oligomers by purified recombinant protein strategies for studying oligomer conformations and their toxicity. Still, there is no specific toxic tau protein has been identified 35 . However, some cellular biosensor technology has been discovered to monitor the formation of tau oligomers and aggregates in the living cells 35 , e.g., fluorescence resonance energy transfer (FRET), bimolecular fluorescence complementation (BiFC), and split luciferase complementation (SLC).…”
Section: Resultsmentioning
confidence: 99%
“…Despite significant improvements, the existing biosensors still have limitations either in terms of sensitivity (i.e. microscopy or western blot for visualization of small tau oligomers), of laborious data analysis (FRET-based assays), or of high-throughput screening compatibility (17). In order to develop improved tau biosensors for research and drug discovery application we used the recently developed highly sensitive Nanoluciferase (Nluc) binary technology (NanoBiT) (18,19).…”
Section: Introductionmentioning
confidence: 99%