Membrane-protein crystallization in cubo: Temperature-dependent phase behaviour of monoolein-detergent mixtures

The lipidic cubic phase of monoolein has proved to be a matrix well suited to the production of three-dimensional crystals of membrane proteins. It consists of a single continuous bilayer, which is contorted in three-dimensional space and separates two distinct water channels. It has previously been proposed that on the addition of precipitants, membrane proteins embedded in the cubic phase migrate through the matrix to nucleation sites and that this process is dependent upon the stability of the lipidic cubic phase. Here, the effect of detergent type (C-8-C-12 glucosides, C-8-C-12 maltosides and C-7 thioglucoside) and concentration (1-3 x the critical micelle concentration; CMC) on cubic phase stability are reported in the form of the temperature-dependent phase behaviour (268-313 K) in 40% aqueous solution. The results are tabulated to show the best monoolein (MO)-detergent mixtures, mixing temperatures and crystallization temperatures identified. Monoolein-detergent mixtures suited for low-temperature in cubo crystallization of temperature-sensitive proteins are also reported for the first time. These mixtures can be prepared at low temperatures (mixed at less than or equal to 288 K) and remain stable at 277 K for a period of at least one month. They include MO- heptyl thioglucoside (1x and 3x CMC), MO-nonyl glucoside (3 x CMC), MO-octyl maltoside (3 x CMC), MO-nonyl maltoside (1 x CMC) and MO-decyl maltoside (1 x CMC)

Studies of lyotropic phases out of equilibrium

EThOS - Electronic Theses Online ServiceGBUnited Kingdo

Harmonic response from microscopic antibubbles

International audienceAn antibubble is a gas bubble containing a liquid droplet core. Both the droplet and the gas bubble are typically surrounded by stabilising shells. Owing to electrostatic forces exerted by these shells, core droplets of micrometer diameter do not readily coalesce with the surrounding liquid medium. Owing to the incompressibility of the liquid droplet core, antibubbles will oscillate asymmetrically, i.e., the radial excursion amplitude of the surface is greater during expansion than during contraction, when subjected to diagnostic ultrasound. Consequently, the harmonic content of the ultrasound signal radiated from antibubbles must be higher than that from identical bubbles without a liquid core. Whether the harmonic signal component generated by physical antibubbles is higher than the harmonic component of identical bubbles without a core has been studied here. We subjected prefabricated antibubbles and identical bubbles without core droplets to 1-MHz ultrasound and to a commercial ultrasound system, and recorded the spectra with a broadband transducer oriented perpendicularly to the transmitter. Normalised by the acoustic response from the medium, the antibubble signal shows stronger higher harmonics than the reference signal, and negligible fundamental response. In conclusion, antibubbles are suitable candidates for harmonic imaging. The generation of higher harmonics without fundamental has been attributed to asymmetric antibubble expansion

Evaluation of chirp reversal power modulation sequence for contrast agent imaging

International audienc

声学泡、反泡泡和细胞

International audienc

Microbubble-mediated ultrasound drug-delivery and therapeutic monitoring

International audienc