Format

Send to

Choose Destination
Mol Cell Endocrinol. 2007 Jun 30;272(1-2):77-85. Epub 2007 May 3.

Refolding of misfolded mutant GPCR: post-translational pharmacoperone action in vitro.

Author information

1
Divisions of Neuroscience and Reproductive Sciences, Oregon National Primate Research Center, Beaverton, OR 97006, USA.

Abstract

All reported GnRH receptor mutants (causing human hypogonadotropic hypogonadism) are misfolded proteins that cannot traffic to the plasma membrane. Pharmacoperones correct misfolding and rescue mutants, routing them to the plasma membrane where they regain function. Because pharmacoperones are often peptidomimetic antagonists, these must be removed for receptor function after rescue; in vivo this necessitates pulsatile pharmacoperone administration. As an antecedent to in vivo studies, we determined whether pharmacoperones need to be present at the time of synthesis or whether previously misfolded proteins could be refolded and rescued. Accordingly, we blocked either protein synthesis or intra-cellular transport. Biochemical and morphological studies using 12 mutants and 10 pharmacoperones representing three different chemical classes show that previously synthesized mutant proteins, retained by the quality control system (QCS), are rescued by pharmacoperones, showing that pharmacoperone administration in vivo likely need not consider whether the target protein is being synthesized at the time of drug administration.

PMID:
17555869
PMCID:
PMC2169380
DOI:
10.1016/j.mce.2007.04.012
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Elsevier Science Icon for PubMed Central
Loading ...
Support Center