Pharmacological chaperones:: a new twist on receptor folding

被引:191
|
作者
Morello, JP
Petäjä-Repo, UE
Bichet, DG
Bouvier, M
机构
[1] Univ Montreal, Dept Biochem, Montreal, PQ H3C 3J7, Canada
[2] Univ Oulu, Dept Anat & Cell Biol, FIN-90014 Oulu, Finland
[3] Hop Sacre Coeur, Ctr Rech, Montreal, PQ H4J 1C5, Canada
[4] Hop Sacre Coeur, Serv Nephrol, Montreal, PQ H4J 1C5, Canada
关键词
D O I
10.1016/S0165-6147(00)01575-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein misfolding is at the root of several genetic human diseases. These diseases do not stem from mutations within the active domain of the proteins, but from mutations that disrupt their three-dimensional conformation, which leads to their intracellular retention by the quality control apparatus of the cell. Facilitating the escape of the mutant proteins from the quality control system by lowering the temperature of the cells or by adding chemicals that assist folding (chemical chaperones) can result in proteins that are fully functional despite their mutation. The discovery that ligands with 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'.
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页码:466 / 469
页数:4
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