Pharmacological chaperones: a new twist on receptor folding

Citation
Jp. Morello et al., Pharmacological chaperones: a new twist on receptor folding, TRENDS PHAR, 21(12), 2000, pp. 466-469
Citations number
25
Categorie Soggetti
Pharmacology & Toxicology
Volume
21
Issue
12
Year of publication
2000
Pages
466 - 469
Database
ISI
SICI code
Abstract
Protein misfolding is at the root of several genetic human diseases. These diseases do not stem from mutations within the active domain of the protein s, but from mutations that disrupt their three-dimensional conformation, wh ich leads to their intracellular retention by the quality control apparatus of the cell. Facilitating the escape of the mutant proteins from the quali ty control system by lowering the temperature of the cells or by adding che micals that assist folding (chemical chaperones) can result in proteins tha t are fully functional despite their mutation. The discovery that ligands w ith pharmacological selectivity (pharmacological chaperones) can rescue the proper targeting and function of misfolded proteins, including receptors, might help to develop new treatments for 'conformational diseases'.