Membrane-integration characteristics of two ABC transporters, CFTR and P-glycoproteinShow others and affiliations
2009 (English)In: Journal of Molecular Biology, ISSN 0022-2836, E-ISSN 1089-8638, Vol. 387, no 5, p. 1153-1164Article in journal (Refereed) Published
Abstract [en]
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.
Place, publisher, year, edition, pages
2009. Vol. 387, no 5, p. 1153-1164
Keywords [en]
cystic fibrosis transmembrane conductance regulator (CFTR), cystic fibrosis (CF), P-glycoprotein (P-gp), membrane protein, topology
National Category
Biochemistry Molecular Biology
Identifiers
URN: urn:nbn:se:su:diva-33929DOI: 10.1016/j.jmb.2009.02.035ISI: 000265501000010PubMedID: 19236881OAI: oai:DiVA.org:su-33929DiVA, id: diva2:283821
2009-12-302009-12-302025-02-20Bibliographically approved