Evidence map›Paper›PMID 40881400›Full record

ReviewJACS Au2025

Lysine-Targeting Inhibitors of Amyloidogenic Protein Aggregation: A Promise for Neurodegenerative Proteinopathies.

Kazuma Murakami, Thi Hong Van Nguyen, Chioko Nagao, Kenji Mizuguchi, Gal Bitan

Abstract readReview
In one paragraph

Review in JACS Au, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

5 authors.

Kazuma MurakamiDivision of Food Science and Biotechnology, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.ORCID https://orcid.org/0000-0003-3152-1784
Thi Hong Van NguyenDivision of Food Science and Biotechnology, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.ORCID https://orcid.org/0000-0003-2133-9161
Chioko NagaoInstitute for Protein Research, Osaka University, Osaka 565-0871, Japan.ORCID https://orcid.org/0000-0002-7721-0642
Kenji MizuguchiInstitute for Protein Research, Osaka University, Osaka 565-0871, Japan.ORCID https://orcid.org/0000-0003-3021-7078
Gal BitanDepartment of Neurology, David Geffen School of Medicine, Brain Research Institute, and Molecular Biology Institute, University of California Los Angeles, Los Angeles, California 90095-7334, United States.ORCID https://orcid.org/0000-0001-7046-3754

Funding

Biomarkers for parkinsonian disorders in CNS-originating extracellular vesiclesRF1NS126406 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BITAN, GAL · 2023 to 2024
$2.6M
Biomarkers for parkinsonian disorders in CNS-originating extracellular vesiclesR01NS126406 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GAL BITAN · 2026 to 2026
$769k
Can diagnostic biomarkers for parkinsonian syndromes be measured in postmortem blood samples?R21NS130326 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BITAN, GAL · 2023 to 2023
$444k
NINDS NIH HHS R01 NS126406NINDS NIH HHS R21 NS130326NINDS NIH HHS RF1 NS126406
6 · The paper itself

Abstract

Inhibition of amyloidogenic-protein oligomerization and aggregation is a promising therapy-development strategy for proteinopathies, such as Alzheimer's and Parkinson's diseases, in which proteins self-associate into a variety of abnormal, toxic assemblies. Despite discovery of numerous compounds modulating the self-assembly process in vitro, few have reached advanced clinical trials, and none have translated into effective therapy to date. A potential reason is a lack of clear mechanistic understanding of the interaction between the inhibitors/modulators and the target metastable protein assemblies. A unique class of compounds targets specifically Lys residues, which have been shown to be important mediators of many amyloidogenic-protein aberrant self-assembly processes due to their participation in both electrostatic and hydrophobic interactions. Although seemingly paradoxical, as these compounds do not target a specific protein, compounds targeting Lys show a remarkable ability to selectively disrupt the interactions mediating abnormal protein self-assembly. Such compounds include covalent and noncovalent Lys-binding small molecules, as well as agents controlling Lys-post-translational modification (PTM). Recent advances in this area show that the application of Lys-targeting inhibitors in antiamyloid drug discovery campaigns and Lys-reactive rational-design approaches have led to intriguing results in multiple systems, including animal models of various proteinopathies. As this strategy is applicable and promising for targeting most of the proteins involved in proteinopathies, including amyloid β-protein, tau, and α-synuclein, here we highlight Lys-binding inhibitors of abnormal protein self-assembly leading to preclinical therapeutic applications for the central nervous system.

Indexed as

Alzheimer’s diseaseamyloidcovalent drugmass spectrometryNMRParkinson’s diseasepost-translational modificationtauopathy

Identifiers

PMID40881400
PMCPMC12381728

What OpenQuestion holds

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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.