Evidence map›Paper›PMID 38816762›Full record

ArticleMolecular neurodegeneration2024

Single-domain antibody-based protein degrader for synucleinopathies.

Yixiang Jiang, Yan Lin, Amber M Tetlow, Ruimin Pan, Changyi Ji, Xiang-Peng Kong, Erin E Congdon, Einar M Sigurdsson

Abstract read
In one paragraph

Article in Molecular neurodegeneration, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Yixiang JiangDepartment of Neuroscience and Physiology, and Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Yan LinDepartment of Neuroscience and Physiology, and Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Amber M TetlowDepartment of Neuroscience and Physiology, and Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Ruimin PanDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Changyi JiDepartment of Neuroscience and Physiology, and Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Xiang-Peng KongDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Erin E CongdonDepartment of Neuroscience and Physiology, and Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Einar M SigurdssonDepartment of Neuroscience and Physiology, and Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, 10016, USA. einar.sigurdsson@nyulangone.org.ORCID 0000-0003-1451-0952

Funding

Research Supplement to Promote Diversity in Health-Related ResearchR01AG032611 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Einar M Sigurdsson · 2008 to 2026
$9.7M
Epitope-Specific Targeting of Tau Aggregates.R01NS077239 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Einar M Sigurdsson · 2011 to 2026
$7.9M
Cell-Type Specific Vulnerability to Tauopathy and Its Prevention in Multiple ModelsRF1NS120488 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RYOO, HYUNG D, SIGURDSSON, EINAR M · 2021 to 2021
$2.4M
Single domain antibodies for diagnosis and treatment of synucleinopathiesR56AG083436 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SIGURDSSON, EINAR M · 2023 to 2023
$717k
Efficacy and Mechanism of Action of Heavy-Chain α-Synuclein Antibody Fragments Derived from LlamaR21AG059391 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SIGURDSSON, EINAR M · 2018 to 2019
$466k
Alzheimer's Association AARF-22-924783Foundation for the National Institutes of Health R56 AG083436-01NIA NIH HHS R01 AG032611NIA NIH HHS R21 AG059391NIA NIH HHS R56 AG083436NINDS NIH HHS R01 NS077239NINDS NIH HHS RF1 NS120488
6 · The paper itself

Abstract

Synucleinopathies are a group of neurodegenerative diseases characterized by the accumulation of α-synuclein (α-syn) in the brain, leading to motor and neuropsychiatric symptoms. Currently, there are no known cures for synucleinopathies, and treatments mainly focus on symptom management. In this study, we developed a single-domain antibody (sdAb)-based protein degrader with features designed to enhance proteasomal degradation of α-syn. This sdAb derivative targets both α-syn and Cereblon (CRBN), a substrate-receptor for the E3-ubiquitin ligase CRL4

Indexed as

alpha-SynucleinSynucleinopathiesAnimalsBrainDisease Models, AnimalHumansMiceProteasome Endopeptidase ComplexSingle-Domain Antibodiesalpha-SynucleinProteasome Endopeptidase ComplexSingle-Domain Antibodies

Identifiers

PMID38816762
PMCPMC11140919

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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.