Mitochondrial dynamics and proteins related to neurodegenerative diseases

Athanasios Alexiou*, Bilal Nizami, Faez Iqbal Khan, Georgia Soursou, Charalampos Vairaktarakis, Stylianos Chatzichronis, Vasilis Tsiamis, Vasileios Manztavinos, Nagendra Sastry Yarla, Ghulam Md Ashraf

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

34 Citations (Scopus)

Abstract

Disruptions in the regulation of mitochondrial dynamics and the occurrence of proteins misfolding lead to neuronal death, resulting in Age-related Dementia and Neurodegenerative diseases as well as Frailty. Functional, neurophysiologic and biochemical alterations within the mitochondrial populations can reveal deficits in brain energy metabolism resulting in Mild Cognitive Impairment, abnormal neural development, autonomic dysfunction and other mitochondrial disorders. Additionally, in cases of Alzheimer’s disease or Parkinson’s disease, a significant number of proteins seem to form unordered and problematic structures, leading through unknown mechanisms to pathological conditions. While the proteins structure prediction problem is still an open challenge regarding its complexity, several features associated with the correlations of misfolding proteins and Neurodegeneration are discussed in the present study and a computational analysis for the proteins Amyloid Beta, Tau, α-Synuclein, Parkin, Pink1, MFN1, MFN1, OPA1, and DNM1L is also presented.

Original languageEnglish
Pages (from-to)850-857
Number of pages8
JournalCurrent Protein and Peptide Science
Volume19
Issue number9
DOIs
Publication statusPublished - 2018
Externally publishedYes

Keywords

  • Alzheimer’s disease
  • Amyloid beta
  • CMT2A
  • DNM1L
  • Huntington's disease
  • MFN1
  • MFN2
  • Mitochondrial dynamics
  • Mitochondrial lesions
  • Neurodegeneration
  • OPA1
  • PINK1
  • Parkin
  • Parkinson’s disease
  • Proteins misfolding
  • Reactive oxygen species
  • Tau
  • α-synuclein

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