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Membrane-integration Characteristics of Two ABC Transporters, CFTR and P-glycoprotein
Authors:Karl Enquist  Mawritz Fransson  Carolina Boekel  Inger Bengtsson  Lisa Lang  Sofia Johansson  IngMarie Nilsson
Affiliation:1 Center for Biomembrane Research, Department of Biochemistry and Biophysics, Stockholm University, SE-106 91 Stockholm, Sweden
2 Stockholm Bioinformatics Center, AlbaNova, SE-106 91 Stockholm, Sweden
Abstract:To what extent do corresponding transmembrane helices in related integral membrane proteins have different membrane-insertion characteristics? Here, we compare, side-by-side, the membrane insertion characteristics of the 12 transmembrane helices in the adenosine triphosphate-binding cassette (ABC) transporters, P-glycoprotein (P-gp) and the cystic fibrosis transmembrane conductance regulator (CFTR). Our results show that 10 of the 12 CFTR transmembrane segments can insert independently into the ER membrane. In contrast, only three of the P-gp transmembrane segments are independently stable in the membrane, while the majority depend on the presence of neighboring loops and/or transmembrane segments for efficient insertion. Membrane-insertion characteristics can thus vary widely between related proteins.
Keywords:CF  cystic fibrosis  CFTR  cystic fibrosis transmembrane conductance regulator  P-gp  P-glycoprotein  TM  transmembrane  ABC transporter  ATP-binding cassette transporter  ER  endoplasmic reticulum  CRM  column-washed dog pancreas rough microsomes  Lep  leader peptidase
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