Coexistence between fluid and crystalline phases of proteins in photosynthetic membranes

TL;DR

This study models protein interactions in photosynthetic membranes, revealing a phase transition between fluid and crystalline states that explains the formation of ordered arrays and their potential functional significance.

Contribution

Introduces a coarse-grained model that reproduces experimental structural features and uncovers a fluid-crystal phase transition in photosynthetic membrane proteins.

Findings

Reproduces experimental protein array structures

Identifies a broad fluid-crystal coexistence region

Suggests membranes operate near phase coexistence

Abstract

Photosystem II (PSII) and its associated light-harvesting complex II (LHCII) are highly concentrated in the stacked grana regions of photosynthetic thylakoid membranes. Within the membrane, PSII-LHCII supercomplexes can be arranged in disordered packings, ordered arrays, or mixtures thereof. The physical driving forces underlying array formation are unknown, complicating attempts to determine a possible functional role for arrays in regulating light harvesting or energy conversion efficiency. Here we introduce a coarse-grained model of protein interactions in coupled photosynthetic membranes, focusing on just two particle types that feature simple shapes and potential energies motivated by structural studies. Reporting on computer simulations of the model's equilibrium fluctuations, we demonstrate its success in reproducing diverse structural features observed in experiments, including extended PSII-LHCII arrays. Free energy calculations reveal that the appearance of arrays marks a phase transition from the disordered fluid state to a system-spanning crystal, which can easily be arrested by thermodynamic constraints or slow dynamics. The region of fluid-crystal coexistence is broad, encompassing much of the physiologically relevant parameter regime. Our results suggest that grana membranes lie at or near phase coexistence, conferring significant structural and functional flexibility to this densely packed membrane protein system.