SANS reveals thylakoid organization in Symbiodinium from coral hosts, suggesting implications for coral bleaching.
We demonstrate that small-angle neutron scattering (SANS) can resolve the architecture of photosynthetic thylakoid membranes in live symbiotic algal cells, both extracted from and living inside their respective hosts ( ex hospite and in hospite , respectively). This enables a new non-destructive approach to probing thylakoid organization in coral symbioses, relevant to understanding the mechanisms of coral bleaching. A biologically realistic triple-vesicle model, guided by electron microscopy and established biochemical constraints, was fitted to SANS data from live Symbiodinium associated with both the coral analogue Aiptasia and the reef-building coral Acropora . The resulting compartment scattering length densities, together with established biochemical constraints, define a limited compositional range that supports the plausibility of the structural solution. These fits capture key scattering features and yield dimensional parameters, including inter-thylakoid (IT) gap widths, with uncertainties small enough to test models of stress-related membrane rearrangement. A focused covariance analysis shows that this SANS framework can resolve an IT-gap expansion of ∼2.4 nm with >7σ sensitivity, sufficient to distinguish structural changes proposed in thylakoid stress-response models. This provides a robust baseline for future live-cell studies.
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Corkery et al. (2025) studied this question.
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