The self-assembled bilayer lipid membrane (BLM) is the basic component of the cell membrane. The reconstitution of ion channel proteins in artificially formed BLMs represents a well-defined system for the functional analysis of ion channels and screening the effects of drugs that act on them. However, because BLMs are unstable, this limits the experimental throughput of BLM reconstitution systems. Here we report on the formation of mechanically stable solvent-free BLMs in microfabricated apertures with defined nano- and micro-tapered edge structures. The role of such nano- and micro-tapered structures on the stability of the BLMs was also investigated. Finally, this BLM system was combined with a cell-free synthesized human ether-a-go-go-related gene channel, a cardiac potassium channel whose relation to arrhythmic side effects following drug treatment is well recognized. Such stable BLMs as these, when combined with a cell-free system, represent a potential platform for screening the effects of drugs that act on various ion-channel genotypes.

Artificially formed bilayer lipid membranes (BLMs) provide well-defined systems for functional analyses of various membrane proteins, including ion channels. However, difficulties associated with the integration of membrane proteins into BLMs limit the experimental efficiency and usefulness of such BLM reconstitution systems. Here, we report on the use of centrifugation to more efficiently reconstitute human ion channels in solvent-free BLMs. The method improves the probability of membrane fusion. Membrane vesicles containing the human ether-a-go-go-related gene (hERG) channel, the human cardiac sodium channel (Na v 1.5), and the human GABA A receptor (GABA A R) channel were formed, and the functional reconstitution of the channels into BLMs via vesicle fusion was investigated. Ion channel currents were recorded in 67% of the BLMs that were centrifuged with membrane vesicles under appropriate centrifugal conditions (14-55 Â g). The characteristic channel properties were retained for hERG, Na v 1.5, and GABA A R channels after centrifugal incorporation into the BLMs. A comparison of the centrifugal force with reported values for the fusion force revealed that a centrifugal enhancement in vesicle fusion was attained, not by accelerating the fusion process but by accelerating the delivery of membrane vesicles to the surface of the BLMs, which led to an increase in the number of membrane vesicles that were available for fusion. Our method for enhancing the probability of vesicle fusion promises to dramatically increase the experimental efficiency of BLM reconstitution systems, leading to the realization of a BLM-based, high-throughput platform for functional assays of various membrane proteins.

Annealing process is crucial in obtaining high-quality perovskite layers used for highly efficient planar perovskite solar cells. In this study, we have investigated annealing-induced chemical and structural changes of tri-iodide (TI) and mixed-halide (MH) organometal perovskite layers using infrared absorption spectroscopy, scanning electron microscopy and x-ray diffraction measurements. For TI layers, the solvent molecule, dimethylformamide (DMF), remained in the form of PbI2/ DMF compound after drying at room temperature. During annealing, the DMF evaporated to form PbI2 crystals. When the MH perovskite film was annealed, both CH3NH3PbCl3 and CH3NH3PbI3 crystals were initially formed from an amorphous phase. With further annealing, the CH3NH3PbI3 crystals gradually grew through the incorporation of source materials supplied from the CH3NH3PbCl3 crystals and the amorphous phase and the slow evaporation of methylammonium (MA) and chloride ions. The resultant MH perovskite layer after annealing was mainly composed of large CH3NH3PbI3 grains with a trace of chloride ions. We suggest that the difference in composition and structure leads to different charge transporting properties of the TI and MH perovskite layers.