Theoretical study of the influence of the photosynthetic membrane on B800-B850 energy transfer within the peripheral light-harvesting complex LH2

TL;DR

This theoretical study investigates how the photosynthetic membrane environment influences intra-complex energy transfer in LH2, revealing increased transfer rates and delocalisation in membrane conditions, aligning with experimental observations.

Contribution

The paper provides a detailed theoretical analysis of how membrane embedding affects excitonic structure and energy transfer dynamics in LH2, highlighting the role of lipid composition.

Findings

Membrane environment increases excitonic delocalisation in LH2.

B800 to B850 energy transfer rate is 30% faster in membrane conditions.

Lipid composition influences the broadening of transfer rate distributions.

Abstract

Photosynthetic organisms rely on a network of light-harvesting protein-pigment complexes to efficiently absorb sunlight and transfer excitation energy to reaction center proteins for charge separation. In photosynthetic purple bacteria, these complexes are embedded in the cell membrane, where lipid composition affects their clustering and inter-complex energy transfer. However, the lipid bilayer's impact on intra-complex excitation dynamics is less understood. Recent experiments compared photo-excitation dynamics in detergent-isolated light harvesting complex 2 (LH2) to LH2 embedded in membrane discs mimicking the biological environment, revealing differences in spectra and intra-complex energy transfer rates. We use available quantum chemical and spectroscopy data to develop a complementary theoretical study on the excitonic structure and intra-complex energy transfer kinetics of the LH2 from photosynthetic purple bacteria Rhodoblastus acidophilus in two conditions: LH2 in a membrane environment and detergent-isolated LH2. Dark excitonic states crucial for B800-B850 energy transfer within LH2 are found to be more delocalised in the membrane model. Using non-perturbative and generalised F\"orster calculations, it is shown that the increased quantum delocalisation leads to a B800 to B850 transfer rate 30% faster than in the detergent-isolated complex, consistent with experimental results. We identify the main energy transfer pathways in each environment and show how differences in the B800 to B850 transfer rate stem from changes in LH2's electronic properties when embedded in the membrane. By considering quasi-static variations of electronic excitation energies in LH2, we show that the broadening of the B800 to B850 transfer rate distribution is affected by lipid composition. We argue that the variation in broadening could indicate a speed-accuracy trade-off, common in biological systems.