Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion.

Article Details

Citation

Chang XB, Hou YX, Jensen TJ, Riordan JR

Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion.

J Biol Chem. 1994 Jul 15;269(28):18572-5.

PubMed ID
7518437 [ View in PubMed
]
Abstract

Technical difficulties in obtaining three-dimensional structures of intrinsic membrane proteins continues to limit understanding of their function. However, considerable insight can be gained from their two-dimensional topological arrangement in the lipid bilayer. Efficient molecular genetic approaches are available to discern the topology of prokaryotic but not of eukaryotic membrane proteins. The absolute asymmetry of the sidedness of their N-glycosylation was employed here to develop such a method using the cystic fibrosis transmembrane conductance regulator (CFTR). Insertion by in vitro mutagenesis of N-glycosylation consensus sequences (NXS/T) in predicted cytoplasmic and extracytoplasmic loops between hydrophobic sequences capable of traversing the membrane established the membrane topology of CFTR. This provides the first experimental evaluation of the original topological model of CFTR based solely on hydropathy algorithms and a method which may be generally applicable for the in vivo evaluation of the topology of other mammalian membrane proteins.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Cystic fibrosis transmembrane conductance regulatorP13569Details