posted on 2024-05-17, 19:06authored bySam Wilson, Charlea D. Clarke, M. Alejandra Carbajal, Roberto Buccafusca, Roland A. Fleck, Vangelis Daskalakis, Alexander V. Ruban
The ability to harvest light effectively in a changing
environment
is necessary to ensure efficient photosynthesis and crop growth. One
mechanism, known as qE, protects photosystem II (PSII) and regulates
electron transfer through the harmless dissipation of excess absorbed
photons as heat. This process involves reversible clustering of the
major light-harvesting complexes of PSII (LHCII) in the thylakoid
membrane and relies upon the ΔpH gradient and the allosteric
modulator protein PsbS. To date, the exact role of PsbS in the qE
mechanism has remained elusive. Here, we show that PsbS induces hydrophobic
mismatch in the thylakoid membrane through dynamic rearrangement of
lipids around LHCII leading to observed membrane thinning. We found
that upon illumination, the thylakoid membrane reversibly shrinks
from around 4.3 to 3.2 nm, without PsbS, this response is eliminated.
Furthermore, we show that the lipid digalactosyldiacylglycerol (DGDG)
is repelled from the LHCII-PsbS complex due to an increase in both
the pKa of lumenal residues and in the
dipole moment of LHCII, which allows for further conformational change
and clustering in the membrane. Our results suggest a mechanistic
role for PsbS as a facilitator of a hydrophobic mismatch-mediated
phase transition between LHCII-PsbS and its environment. This could
act as the driving force to sort LHCII into photoprotective nanodomains
in the thylakoid membrane. This work shows an example of the key role
of the hydrophobic mismatch process in regulating membrane protein
function in plants.