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We advanced a previously reported model for the \textit{in situ} scatteringdata analysis of coexisting lipid domains in free-floating multilamellarvesicles. Based on the scattering density profile of the individual domains weconsidered in particular modifications due to positionally anticorrelateddomains or the presence of cholesterol. The latter aspect can be easilyextended to any other lipophilic molecule. This allowed us to retrieve elasticand structural details (bending fluctuations, domain thickness, area per lipid)of coexisting liquid-ordered/liquid-disordered domains, including thepartitioning of cholesterol from small-angle x-ray scattering experiments.Moreover, the model also successfully fitted data of multilamellar vesiclesexhibiting nanoscopic domains, which displayed unlike coexisting micron-sizeddomains no clear signal for two lamellar lattices. Our results indicate apreviously not observed translation of cholesterol toward the bilayer center ofnanoscopic liquid-ordered domains.

High-resolution structure of coexisting nanoscopic and microscopic lipid domains