4.6 Article

A proteoliposome-based system reveals how lipids control photosynthetic light harvesting

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 295, Issue 7, Pages 1857-1866

Publisher

ELSEVIER
DOI: 10.1074/jbc.RA119.011707

Keywords

photosynthesis; membrane biophysics; membrane lipid; lipid-protein interaction; light-harvesting complex (antenna complex); lateral membrane pressure; non-bilayer lipid; non-photochemical quenching; proteoliposome; thylakoid membrane; monogalactosyldiacylglycerol; energy transduction; photosystem

Funding

  1. National Science Foundation [MCB1616982]
  2. U.S. Department of Energy [DE-SC 0017160]
  3. U.S. Department of Agriculture, National Institute of Food and Agriculture Hatch Projects [1005351, 0119]
  4. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC0205CH11231]
  5. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy [DE-AC03-76SF000098, FWP 449B]
  6. NIFA [812083, 1005351] Funding Source: Federal RePORTER

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Integral membrane proteins are exposed to a complex and dynamic lipid environment modulated by nonbilayer lipids that can influence protein functions by lipid-protein interactions. The nonbilayer lipid monogalactosyldiacylglycerol (MGDG) is the most abundant lipid in plant photosynthetic thylakoid membranes, but its impact on the functionality of energy-converting membrane protein complexes is unknown. Here, we optimized a detergent-based reconstitution protocol to develop a proteoliposome technique that incorporates the major light-harvesting complex II (LHCII) into compositionally well-defined large unilamellar lipid bilayer vesicles to study the impact of MGDG on light harvesting by LHCII. Using steady-state fluorescence spectroscopy, CD spectroscopy, and time-correlated single-photon counting, we found that both chlorophyll fluorescence quantum yields and fluorescence lifetimes clearly indicate that the presence of MGDG in lipid bilayers switches LHCII from a light-harvesting to a more energy-quenching mode that dissipates harvested light into heat. It is hypothesized that in the in vitro system developed here, MGDG controls light harvesting of LHCII by modulating the hydrostatic lateral membrane pressure profile in the lipid bilayer sensed by LHCII-bound peripheral pigments.

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