Deciphering the role of individual acyl chains in the interaction network between phosphatidylserines and a single-spanning membrane protein

Biochemistry. 2002 Nov 19;41(46):13611-6. doi: 10.1021/bi026274b.

Abstract

PMP1 is a small single-spanning membrane protein functioning as a regulatory subunit of the yeast plasma membrane H(+)-ATPase. This protein forms a unique helix and exhibits a positively charged cytoplasmic domain that is able to specifically segregate phosphatidylserines (PSs). A marked groove formed at the helix surface is thought to play a major role in the related lipid-protein interaction network. Mutational analysis and (1)H NMR experiments were therefore performed on a synthetic PMP1 fragment using DPC-d(38) micelles as a membrane-like environment, in the presence of small amounts of POPS. A mutation designed for altering the helix groove was shown to disfavor the POPS binding specificity as much as that affecting the electrostatic interaction network. From POPS titration experiments monitored by a full set of one- and two-dimensional NOESY spectra, the association between the phospholipids and the PMP1 peptide has been followed. Our data reveal that the clustering of POPS molecules is promoted from a stabilized framework obtained by coupling the PMP1 helix groove to a POPS sn-2 chain. To our knowledge, the NOE-based titration plots displayed in this report constitute the first NMR data that directly distinguish the role of the sn-1 and sn-2 acyl chains in a lipid-protein interaction. The results are discussed while taking into account our accurate knowledge of the yeast plasma membrane composition and its ability to form functional lipid rafts.

MeSH terms

  • Amino Acids / chemistry
  • Cell Membrane / chemistry
  • DNA Mutational Analysis
  • Fungal Proteins / chemistry
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism*
  • Lipid Bilayers / chemistry
  • Lipid Bilayers / metabolism
  • Lipid Metabolism
  • Lipids / chemistry
  • Magnetic Resonance Spectroscopy
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Micelles
  • Models, Chemical
  • Mutation
  • Nerve Tissue Proteins*
  • Peptide Fragments / chemistry
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Phosphatidylserines / chemistry
  • Phosphatidylserines / metabolism*
  • Protein Binding
  • Protein Conformation
  • Proteolipids / chemistry
  • Proteolipids / genetics
  • Proteolipids / metabolism*
  • Proton-Translocating ATPases
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins*

Substances

  • Amino Acids
  • Fungal Proteins
  • Lipid Bilayers
  • Lipids
  • Membrane Proteins
  • Micelles
  • Nerve Tissue Proteins
  • PMP1 protein, S cerevisiae
  • Peptide Fragments
  • Phosphatidylserines
  • Proteolipids
  • Saccharomyces cerevisiae Proteins
  • Proton-Translocating ATPases