Literature DB >> 23378031

Protein quality control system in neurodegeneration: a healing company hard to beat but failure is fatal.

Deepak Chhangani1, Amit Mishra.   

Abstract

A common feature in most neurodegenerative diseases and aging is the progressive accumulation of damaged proteins. Proteins are essential for all crucial biological functions. Under some notorious conditions, proteins loss their three dimensional native conformations and are converted into disordered aggregated structures. Such changes rise into pathological conditions and eventually cause serious protein conformation disorders. Protein aggregation and inclusion bodies formation mediated multifactorial proteotoxic stress has been reported in the progression of Parkinson's disease (PD), Huntington's disease (HD), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS) and Prion disease. Ongoing studies have been remarkably informative in providing a systematic outlook for better understanding the concept and fundamentals of protein misfolding and aggregations. However, the precise role of protein quality control system and precursors of this mechanism remains elusive. In this review, we highlight recent insights and discuss emerging cytoprotective strategies of cellular protein quality control system implicated in protein deposition diseases. Our current review provides a clear, understandable framework of protein quality control system that may offer the more suitable therapeutic strategies for protein-associated diseases.

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Year:  2013        PMID: 23378031     DOI: 10.1007/s12035-013-8411-0

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  193 in total

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Review 3.  Protein degradation and protection against misfolded or damaged proteins.

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Journal:  Mol Cell       Date:  1998-04       Impact factor: 17.970

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  12 in total

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Review 5.  mTOR in Alzheimer disease and its earlier stages: Links to oxidative damage in the progression of this dementing disorder.

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6.  Ubiquitin ligase ITCH recruitment suppresses the aggregation and cellular toxicity of cytoplasmic misfolded proteins.

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Review 7.  Management of Benign Prostatic Hyperplasia: Could Dietary Polyphenols Be an Alternative to Existing Therapies?

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8.  Mahogunin ring finger-1 (MGRN1) suppresses chaperone-associated misfolded protein aggregation and toxicity.

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Review 9.  Potential Therapeutic Benefits of Maintaining Mitochondrial Health in Peripheral Neuropathies.

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Review 10.  Gp78 E3 Ubiquitin Ligase: Essential Functions and Contributions in Proteostasis.

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