Evidence map›Paper›PMID 37431684›Full record

ArticleJournal of materials chemistry. B2023

Blocking tau transmission by biomimetic graphene nanoparticles.

Runyao Zhu, Kamlesh M Makwana, Youwen Zhang, Benjamin H Rajewski, Juan R Del Valle, Yichun Wang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of materials chemistry. B, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Runyao ZhuDepartment of Chemical & Biomolecular Engineering, University of Notre Dame, Indiana 46556, USA. ywang65@nd.edu.ORCID 0009-0005-5109-0020
Kamlesh M MakwanaDepartment of Chemistry & Biochemistry, University of Notre Dame, Indiana 46556, USA.ORCID 0000-0002-4918-8572
Youwen ZhangDepartment of Chemical & Biomolecular Engineering, University of Notre Dame, Indiana 46556, USA. ywang65@nd.edu.
Benjamin H RajewskiDepartment of Chemistry & Biochemistry, University of Notre Dame, Indiana 46556, USA.ORCID 0000-0002-4750-0331
Juan R Del ValleDepartment of Chemistry & Biochemistry, University of Notre Dame, Indiana 46556, USA.ORCID 0000-0002-8315-5264
Yichun WangDepartment of Chemical & Biomolecular Engineering, University of Notre Dame, Indiana 46556, USA. ywang65@nd.edu.ORCID 0000-0002-4353-6660
University of Notre Dame · US

Funding

Chemical approaches to selectively target beta-rich amyloidsR01AG074570 · NIA · UNIVERSITY OF NOTRE DAME · PI DEL VALLE, JUAN R · 2021 to 2025
$2.5M
NIA NIH HHS R01 AG074570
6 · The paper itself

Abstract

Tauopathies are a class of neurodegenerative diseases resulting in cognitive dysfunction, executive dysfunction, and motor disturbance. The primary pathological feature of tauopathies is the presence of neurofibrillary tangles in the brain composed of tau protein aggregates. Moreover, tau aggregates can spread from neuron to neuron and lead to the propagation of tau pathology. Although numerous small molecules are known to inhibit tau aggregation and block tau cell-to-cell transmission, it is still challenging to use them for therapeutic applications due to poor specificity and low blood-brain barrier (BBB) penetration. Graphene nanoparticles were previously demonstrated to penetrate the BBB and are amenable to functionalization for targeted delivery. Moreover, these nanoscale biomimetic particles can self-assemble or assemble with various biomolecules including proteins. In this paper, we show that graphene quantum dots (GQDs), as graphene nanoparticles, block the seeding activity of tau fibrils by inhibiting the fibrillization of monomeric tau and triggering the disaggregation of tau filaments. This behavior is attributed to electrostatic and π-π stacking interactions of GQDs with tau. Overall, our studies indicate that GQDs with biomimetic properties can efficiently inhibit and disassemble pathological tau aggregates, and thus block tau transmission, which supports their future developments as a potential treatment for tauopathies.

Indexed as

GraphiteQuantum DotsTauopathiesBiomimeticsHumansNeurofibrillary Tanglestau ProteinsGraphitetau Proteins

Identifiers

PMID37431684
PMCPMC10528742
OpenAlexW4383040549

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.