posted on 2018-03-26, 00:00authored byDennis Seiwert, Hannes Witt, Sandra Ritz, Andreas Janshoff, Harald Paulsen
The
thylakoid membrane of algae and land plants is characterized
by its intricate architecture, comprising tightly appressed membrane
stacks termed grana. The contributions of individual components to
grana stack formation are not yet fully elucidated. As an in vitro model, we use supported lipid bilayers made of
thylakoid lipid mixtures to study the effect of major light-harvesting
complex (LHCII), different lipids, and ions on membrane stacking,
seen as elevated structures forming on top of the planar membrane
surface in the presence of LHCII protein. These structures were examined
by confocal laser scanning microscopy, atomic force microscopy, and
fluorescence recovery after photobleaching, revealing multilamellar
LHCII–membrane stacks composed of connected lipid bilayers.
Both native-like and non-native interactions between the LHCII complexes
may contribute to membrane appression in the supported bilayers. However,
applying in vivo-like salt conditions to uncharged
glycolipid membranes drastically increased the level of stack formation
due to enforced LHCII–LHCII interactions, which is in line
with recent crystallographic and cryo-electron microscopic data [Wan,
T., et al. (2014) Mol. Plant 7, 916–919; Albanese,
P., et al. (2017) Sci. Rep. 7, 10067–10083].
Furthermore, we observed the nonbilayer lipid MGDG to strongly promote
membrane stacking, pointing to the long-term proposed function of
MGDG in stabilizing the inner membrane leaflet of highly curved margins
in the periphery of each grana disc because of its negative intrinsic
curvature [Murphy, D. J. (1982) FEBS Lett. 150, 19–26].