Abstract
The last decade has seen a range of studies using non-invasive neutron and X-ray techniques to probe the ultrastructure of a variety of photosynthetic membrane systems. A common denominator in this work is the lack of an explicitly formulated underlying structural model, ultimately leading to ambiguity in the data interpretation. Here we formulate and implement a full mathematical model of the scattering from a stacked double bilayer membrane system taking instrumental resolution and polydispersity into account. We validate our model by direct simulation of scattering patterns from 3D structural models. Most importantly, we demonstrate that the full scattering curves from three structurally typical cyanobacterial thylakoid membrane systems measured in vivo can all be described within this framework. The model provides realistic estimates of key structural parameters in the thylakoid membrane, in particular the overall stacking distance and how this is divided between membranes, lumen and cytoplasmic liquid. Finally, from fitted scattering length densities it becomes clear that the protein content in the inner lumen has to be lower than in the outer cytoplasmic liquid and we extract the first quantitative measure of the luminal protein content in a living cyanobacteria.
Highlights
We demonstrate that the entire neutron scattering curve measured in vivo on three different, but structurally typical cyanobacterial thylakoid membrane systems, are fully described within our model framework
In this paper we have described a straightforward scattering model based on a double-bilayer membrane stack
Our model presents a rationale to explain the entire cyanobacterial scattering pattern as occurring from an ordered lamellar system and we have employed this model to study the ultrastructure of thylakoids inside cyanobacterial cells in vivo
Summary
For this reason there has been several studies using small-angle neutron scattering (SANS) to gain information on photosynthetic membranes, including cyanobacterial thylakoid membranes[9,10,11,12,13,14]. None of the studies makes use of an underlying structural model to fit the full scattering curve, based on the clear fact that the scattering originates from a stacked membrane system. Neither do they include instrument resolution effects which we will show below to be absolutely necessary for correct data interpretation. We estimate cyanobacterial lumenal protein content solely from the scattering model
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