Neurodegenerative Diseases and Related Proteins

A special issue of Cells (ISSN 2073-4409).

Deadline for manuscript submissions: 31 March 2026 | Viewed by 21

Special Issue Editor


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Guest Editor
Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA
Interests: mitochondrial dysfunction; MAM; mitophagy; tauopathy; TDP-43 pathology; Alzheimer’s disease; FTD-ALS; neurodegeneration
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Special Issue Information

Dear Colleagues,

Proteins such as amyloid-β, tau, α-synuclein, TDP-43, huntingtin, and others play central roles in the onset and progression of neurodegenerative diseases. Aberrant conformational changes, disrupted cellular quality control systems, and pathological seeding of misfolded species collectively compromise neuronal homeostasis, leading to synaptic dysfunction, neuroinflammation, and cell death. Recent advances in high-resolution structural biology, single-cell omics, and in vitro/in vivo model systems have begun to unravel the complex interplay between proteostasis networks and neurodegeneration. This Special Issue will showcase studies that dissect these pathways at the molecular level, explore how genetic and environmental factors modulate protein toxicity, and evaluate novel compounds or gene-based therapies aimed at restoring protein homeostasis. By curating a comprehensive collection of articles, we aim to provide researchers and clinicians with a state-of-the-art reference that bridges fundamental discoveries and therapeutic innovation.

Aim & Scope

This Special Issue aims to bring together innovative research on the molecular, cellular, and systemic functions of proteins associated with neurodegenerative diseases. We encourage original articles, reviews, and perspectives that highlight how misfolded, aggregated, or dysfunctional proteins contribute to the pathogenesis of diseases such as Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, Huntington’s disease, frontotemporal dementia, and related disorders. Topics of interest include, but are not limited to, the following:

  • Protein misfolding, aggregation, and propagation;
  • Post-translational modifications and proteostasis;
  • Mitochondrial dysfunction and ER–mitochondria crosstalk;
  • Autophagy, mitophagy, and selective protein clearance;
  • Proteomic and multi-omics approaches to biomarker discovery;
  • Protein–protein interactions and structural biology;
  • Genetic and epigenetic regulation of disease-related proteins;
  • Novel therapeutic strategies targeting proteopathic cascades.

By fostering interdisciplinary contributions—from basic mechanistic studies to translational and clinical research—this issue aims to accelerate our understanding of proteopathic mechanisms and identify new avenues for intervention.

Dr. Tian Liu
Guest Editor

Manuscript Submission Information

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • protein misfolding and aggregation
  • proteostasis and quality control
  • neuroinflammation
  • autophagy and mitophagy
  • molecular chaperones
  • Amyloid-β and tau
  • α-synuclein and TDP-43
  • multi-omics biomarkers
  • structural biology
  • therapeutic targets
  • mitochondrial–ER crosstalk
  • genetic and epigenetic regulation

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Published Papers

This special issue is now open for submission.
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