Spontaneous Reconstitution of Functional Transmembrane Proteins During Bioorthogonal Phospholipid Membrane Synthesis

Angew Chem Int Ed Engl. 2015 Oct 19;54(43):12738-42. doi: 10.1002/anie.201504339. Epub 2015 Aug 28.

Abstract

Transmembrane proteins are critical for signaling, transport, and metabolism, yet their reconstitution in synthetic membranes is often challenging. Non-enzymatic and chemoselective methods to generate phospholipid membranes in situ would be powerful tools for the incorporation of membrane proteins. Herein, the spontaneous reconstitution of functional integral membrane proteins during the de novo synthesis of biomimetic phospholipid bilayers is described. The approach takes advantage of bioorthogonal coupling reactions to generate proteoliposomes from micelle-solubilized proteins. This method was successfully used to reconstitute three different transmembrane proteins into synthetic membranes. This is the first example of the use of non-enzymatic chemical synthesis of phospholipids to prepare proteoliposomes.

Keywords: membrane proteins; phospholipids; proteoliposomes; self-assembly; synthetic biology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Electron Transport Complex IV / chemistry
  • Electron Transport Complex IV / metabolism
  • Lipid Bilayers / chemistry*
  • Lipid Bilayers / metabolism
  • Membrane Proteins / chemistry*
  • Membrane Proteins / metabolism
  • Micelles
  • Phospholipids / chemistry*
  • Phospholipids / metabolism
  • Plasma Membrane Calcium-Transporting ATPases / chemistry
  • Plasma Membrane Calcium-Transporting ATPases / metabolism
  • Proteolipids / chemistry*
  • Proteolipids / metabolism

Substances

  • Lipid Bilayers
  • Membrane Proteins
  • Micelles
  • Phospholipids
  • Proteolipids
  • proteoliposomes
  • Electron Transport Complex IV
  • Plasma Membrane Calcium-Transporting ATPases