Molecular Basis of Proteinopathies in Neurodegenerative Diseases
A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Neurobiology".
Deadline for manuscript submissions: 28 February 2026
Special Issue Editor
Interests: neurodegenerative disease; aging; cognitive impairment; Huntington’s disease; autophagy; innate immunity; PROTAC; nanobody
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
Dear Colleagues,
Protein misfolding and aggregation are central features of many neurodegenerative disorders, including Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, and amyotrophic lateral sclerosis. These proteinopathies disrupt proteostasis, trigger cellular stress responses, and propagate pathology. While their presence has long been recognized, recent advances in molecular biology, structural analysis, proteomics, target protein degradation (TPD), and multi-omics technologies have provided new opportunities to uncover their mechanisms and therapeutic potential.
This Special Issue invites original research, reviews, and short communications addressing the molecular mechanisms underlying protein aggregation, toxicity, and clearance. Topics may include pathogenic protein structures, proteostasis network failure, post-translational modifications, molecular biomarkers, advanced in vitro and in vivo models, and novel therapeutic strategies.
Our goal is to integrate insights from molecular neuroscience, structural biology, and translational research to advance the understanding of proteinopathies and foster the development of targeted interventions for neurodegenerative diseases.
Dr. Kyoung Joo Cho
Guest Editor
Manuscript Submission Information
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Keywords
- protein misfolding
- neurodegenerative diseases
- protein aggregation
- proteostasis
- post-translational modifications
- ubiquitin–proteasome system
- autophagy
- targeted protein degradation
- therapeutic strategies
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