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The application of dynamic light scattering to soft matter systems has strongly profited from advanced approaches such as the so-called modulated 3D cross correlation technique (mod3D-DLS) that suppress contributions from multiple scattering, and can therefore be used for the characterization of turbid samples. Here we now extend the possibilities of this technique to allow for depolarized light scattering (Mod3D-DDLS) and thus obtain information on both translational and rotational diffusion, which is important for the characterization of anisotropic particles. We describe the required optical design and test the performance of the approach for increasingly turbid samples using well defined anisotropic colloidal models systems. Our measurements demonstrate that 3D-DDLS experiments can be performed successfully for samples with a reduced transmission due to multiple scattering as low as 1\%. We compare the results from this approach with those obtained by standard DDLS experiments, and point out the importance of using an appropriate optical design when performing depolarized dynamic light scattering experiments with turbid systems.

Diffusion of proteins on length scales of their own diameter in highly concentrated solutions is essential for understanding the cellular machinery of living cells, but its experimental characterization remains a challenge. While X-ray photon correlation spectroscopy (XPCS) is currently the only technique that in principle allows for a measurement of long-time collective diffusion on these length scales for such systems, its application to protein solutions is seriously hampered by radiation damage caused by the highly intense X-ray beams required for such experiments. Here we apply an experimental design and an analysis strategy that allow us to successfully use XPCS experiments in order to measure collective long-time cage relaxation in highly crowded solutions of the eye lens protein {\alpha}-crystallin close to and beyond dynamical arrest. We also address the problem of radiation-induced damage in such experiments. We demonstrate that radiation effects depend both on the total dose as well as the dose rate of the absorbed radiation, and discuss possible processes and mechanism responsible for the observed radiation effects as well as their consequences for future applications of XPCS in biological systems.

The structure of the ripple phase of phospholipid membranes remains poorly understood in spite of a large number of theoretical studies, with many experimentally established structural features of this phase unaccounted for. In this article we present a phenomenological theory of phase transitions in single- and two-component achiral lipid membranes in terms of two coupled order parameters -- a scalar order parameter describing {\it lipid chain melting}, and a vector order parameter describing the {\it tilt of the hydrocarbon chains} below the chain-melting transition. This model reproduces all the salient structural features of the ripple phase, providing a unified description of the phase diagram and microstructure. In addition, it predicts a variant of this phase which does not seem to have been experimentally observed. Using this model we have calculated generic phase diagrams of two-component membranes. We have also determined the phase diagram of a two-component lipid membrane from x-ray diffraction studies on aligned multilayers. This phase diagram is found to be in good agreement with that calculated from the model., Comment: 10 pages, 10 figures

We report the observation of a novel isotropic phase of amphiphile bilayers in a mixed system consisting of the ionic surfactant, sodium docecylsulphate (SDS), and the organic salt p-toludine hydrochloride (PTHC). This system forms a collapsed lamellar ($L_\alpha$) phase over a wide range of water content, which transforms into an isotropic phase on heating. This transition is not observed in samples without excess water, where the $L_\alpha$ phase is stable at higher temperatures. Our observations indicate that the $L_\alpha$ - isotropic transition is driven by the unbinding of edge dislocation loops and that the isotropic phase in the present attraction-dominated system is the analogue of the sponge phase usually seen in amphiphile systems dominated by interbilayer steric repulsion.

We present a phenomenological theory of phase transitions in achiral lipid membranes in terms of two coupled order parameters -- a scalar order parameter describing lipid chain melting, and a vector order parameter describing the tilt of the hydrocarbon chains below the chain-melting transition. Existing theoretical models fail to account for all the observed features of the phase diagram, in particular the detailed microstructure of the asymmetric ripple phase lying between the fluid and the tilted gel phase. In contrast, our two-component theory reproduces all the salient structural features of the ripple phase, providing a unified description of the phase diagram and microstructure.