Membrane insertion and topology of the amino-terminal domain TMD0 of multidrug-resistance associated protein 6 (MRP6)

FEBS Lett. 2015 Dec 21;589(24 Pt B):3921-8. doi: 10.1016/j.febslet.2015.10.030. Epub 2015 Nov 3.

Abstract

The function of the ATP-binding cassette transporter MRP6 is unknown but mutations in its gene cause pseudoxanthoma elasticum. We have investigated the membrane topology of the N-terminal transmembrane domain TMD0 of MRP6 and the membrane integration and orientation propensities of its transmembrane segments (TMs) by glycosylation mapping. Results demonstrate that TMD0 has five TMs, an Nout-Cin topology and that the less hydrophobic TMs have strong preference for their orientation in the membrane that affects the neighboring TMs. Two disease-causing mutations changing the number of positive charges in the loops of TMD0 did not affect the membrane insertion efficiencies of the adjacent TMs.

Keywords: ABCC6; ATP-binding cassette transporter; Membrane protein insertion; Multidrug-resistance associated protein 6; Pseudoxanthoma elasticum; Transmembrane domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Endoplasmic Reticulum / metabolism
  • Humans
  • Intracellular Membranes / metabolism*
  • Multidrug Resistance-Associated Proteins / chemistry*
  • Multidrug Resistance-Associated Proteins / genetics
  • Multidrug Resistance-Associated Proteins / metabolism*
  • Protein Structure, Tertiary
  • Protein Transport
  • Sequence Deletion

Substances

  • ABCC6 protein, human
  • Multidrug Resistance-Associated Proteins