analysis-protein-folding-transport-degradation-living-cells

Analysis of Protein Folding, Transport, and Degradation in Living Cells by Radioactive Pulse Chase

Radioactive pulse-chase labeling is a powerful tool for studying the conformational maturation, the transport to their functional cellular location, and ...

Utrecht University

Cystic fibrosis is caused by mutations in the  gene, which are subdivided into six classes. Mutants of classes III and IV reach the cell surface but have limited function. Most class-III and class-IV mutants respond well to the recently approved potentiator VX-770, which opens the channel. We here revisited function and folding of some class-IV mutants and discovered that R347P is the only one that leads to major defects in folding. By this criterion and by its functional response to corrector drug VX-809, R347P qualifies also as a class-II mutation. Other class-IV mutants folded like wild-type CFTR and responded similarly to VX-809, demonstrating how function and folding are connected. Studies on both types of defects complement each other in understanding how compounds improve mutant CFTR function. This provides an attractive unbiased approach for characterizing mode of action of novel therapeutic compounds and helps address which drugs are efficacious for each cystic fibrosis disease variant.

Hui Ying Yeoh

Cellular Protein Chemistry

Utrecht University

Analysis of Protein Folding, Transport, and Degradation in Living Cells by Radioactive Pulse Chase

Hui Ying Yeoh

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Cellular Protein Chemistry

Utrecht University

Analysis of Protein Folding, Transport, and Degradation in Living Cells by Radioactive Pulse Chase

Cellular Protein Chemistry