Thylakoid membranes
in the chloroplast of plants, algae, and cyanobacteria
are the powerhouse of photosynthesis, capturing solar energy and converting
it into chemical energy. Although their structures and functions have
been extensively studied, the intrinsically heterogeneous and dynamic
nature of the membrane structures is still not fully understood. Investigating
native thylakoid membranes <i>in vivo</i> is difficult due
to their small size and limited external access to the chloroplast
interior, while the bottom-up approaches based on model systems have
been hampered by the sheer complexity of the native membrane. Here,
we try to fill the gap by reconstituting the whole thylakoid membrane
into a patterned substrate-supported planer bilayer. A mixture of
thylakoid membrane purified from spinach leaves and synthetic phospholipid
1,2-dioleoyl-<i>sn</i>-glycero-3-phosphocholine (DOPC) vesicles
spontaneously formed a laterally continuous and fluid two-dimensional
(2D) membrane in the scaffold of the patterned polymeric bilayer.
Chlorophyll fluorescence arising from photosystem II (PSII) recovered
after photobleaching, suggesting that the membrane components are
laterally mobile. The reversible changes of chlorophyll fluorescence
in the presence of the electron acceptors and/or inhibitors indicated
that the electron transfer activity of PSII was retained. Furthermore,
we confirmed the electron transfer activity of photosystem I (PSI)
by observing the generation of nicotinamide adenine dinucleotide phosphate
(NADPH) in the presence of water-soluble ferredoxin and ferredoxin–NADP<sup>+</sup> reductase. The lateral mobility of membrane-bound molecules
and the functional reconstitution of major photosystems provide evidence
that our hybrid thylakoid membranes could be an excellent experimental
platform to study the 2D molecular organization and machinery of photosynthesis.