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PMID: 10712902 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Specific proteins are required to translocate phosphatidylcholine bidirectionally across the endoplasmic reticulum.

Current biology : CB ·Vol. 10 ·No. 5 ·2000-03-09 ·Pages 241-52

Menon AK, Watkins WE3rd, Hrafnsdóttir S

Abstract

A long-standing problem in understanding the mechanism by which the phospholipid bilayer of biological membranes is assembled concerns how phospholipids flip back and forth between the two leaflets of the bilayer. This question is important because phospholipid biosynthetic enzymes typically face the cytosol and deposit newly synthesized phospholipids in the cytosolic leaflet of biogenic membranes such as the endoplasmic reticulum (ER). These lipids must be transported across the bilayer to populate the exoplasmic leaflet for membrane growth. Transport does not occur spontaneously and it is presumed that specific membrane proteins, flippases, are responsible for phospholipid flip-flop. No biogenic membrane flippases have been identified and there is controversy as to whether proteins are involved at all, whether any membrane protein is sufficient, or whether non-bilayer arrangements of lipids support flip-flop. To test the hypothesis that specific proteins facilitate phospholipid flip-flop in the ER, we reconstituted transport-active proteoliposomes from detergent-solubilized ER vesicles under conditions in which protein-free liposomes containing ER lipids were inactive. Transport was measured using a synthetic, water-soluble phosphatidylcholine and was found to be sensitive to proteolysis and associated with proteins or protein-containing complexes that sedimented operationally at 3.8S. Chromatographic analyses indicated the feasibility of identifying the transporter(s) by protein purification approaches, and raised the possibility that at least two different proteins are able to facilitate transport. Calculations based on a simple reconstitution scenario suggested that the transporters represent approximately 0.2% of ER membrane proteins. Our results clearly show that specific proteins are required to translocate a phosphatidylcholine analogue across the ER membrane. These proteins are likely to be the flippases, which are required to translocate natural phosphatidylcholine and other phospholipids across the ER membrane. The methodology that we describe paves the way for identification of a flippase.

MeSH Terms
Animals Biological Transport Carrier Proteins/metabolism Chromatography, Ion Exchange Detergents/pharmacology Endopeptidase K/pharmacology Endoplasmic Reticulum, Rough/metabolism Liposomes/metabolism Membrane Proteins/metabolism Microscopy, Electron Microsomes, Liver/metabolism Models, Biological Octoxynol/pharmacology Phosphatidylcholines/metabolism Phospholipid Transfer Proteins Proteolipids/metabolism Rats Time Factors
Chemicals
Carrier Proteins Detergents Liposomes Membrane Proteins Phosphatidylcholines Phospholipid Transfer Proteins Proteolipids proteoliposomes Octoxynol Endopeptidase K
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Menon A K
Department of Biochemistry, University of Wisconsin-Madison, Madison, 53706-1569, USA. [email protected].
Watkins WE3rd
Hrafnsdóttir S
Article Info
Journal
Current biology : CB
Abbr.
Curr Biol
ISSN
0960-9822
Published
2000-03-09
Pages
241-52
Language
English
Region
England
NLM ID
9107782
Subset
IM
Grants
NIGMS NIH HHS · GM55427 · United States
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