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Small molecules that target protein misfolding.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2012 Dec 27; Vol. 55 (24), pp. 10823-43. Date of Electronic Publication: 2012 Nov 01. - Publication Year :
- 2012
-
Abstract
- Protein misfolding is a process in which proteins are unable to attain or maintain their biologically active conformation. Factors contributing to protein misfolding include missense mutations and intracellular factors such as pH changes, oxidative stress, or metal ions. Protein misfolding is linked to a large number of diseases such as cystic fibrosis, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, and less familiar diseases such as Gaucher's disease, nephrogenic diabetes insipidus, and Creutzfeldt-Jakob disease. In this Perspective, we report on small molecules that bind to and stabilize the aberrant protein, thereby helping it to attain a native or near-native conformation and restoring its function. The following targets will be specifically discussed: transthyretin, p53, superoxide dismutase 1, lysozyme, serum amyloid A, prions, vasopressin receptor 2, and α-1-antitrypsin.
- Subjects :
- Amyloid metabolism
Animals
Humans
Models, Molecular
Muramidase chemistry
Muramidase physiology
Mutation
Neurodegenerative Diseases metabolism
Prealbumin chemistry
Prealbumin physiology
Prions chemistry
Prions physiology
Protein Binding
Protein Conformation
Proteostasis Deficiencies metabolism
Receptors, Vasopressin chemistry
Receptors, Vasopressin physiology
Serum Amyloid A Protein chemistry
Serum Amyloid A Protein physiology
Small Molecule Libraries pharmacology
Superoxide Dismutase chemistry
Superoxide Dismutase physiology
Superoxide Dismutase-1
Tumor Suppressor Protein p53 chemistry
Tumor Suppressor Protein p53 physiology
Unfolded Protein Response
alpha 1-Antitrypsin chemistry
alpha 1-Antitrypsin physiology
Neurodegenerative Diseases drug therapy
Protein Folding
Proteins chemistry
Proteins physiology
Proteostasis Deficiencies drug therapy
Small Molecule Libraries chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 55
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 23075044
- Full Text :
- https://doi.org/10.1021/jm301182j