Gene expression in on-chip membrane-bound artificial cells.

Artificial cells made of molecular components and lipid membrane are emerging platforms to characterize living systems properties. Cell-free transcription-translation (TXTL) offers advantages for the bottom-up synthesis of cellular reactors. Yet, scaling up their design within well-defined geometries remains challenging. We present a microfluidic device hosting TXTL reactions of a reporter gene in thousands of microwells separated from an external buffer by a phospholipid membrane. In the presence of nutrients in the buffer, micro-reactors are stable beyond 24 hours and yield a few mg/mL of proteins. Nutrients in the external solution feed TXTL reaction at picoliter scale via passive transport across the phospholipid membrane of each microfluidic well, despite the absence of pores. Replacing nutrients with inert polymer and fatty acids at isotonic concentration reduces micro-reactors efficiency, and a significant fraction yields no protein. This emphasizes the crucial role of membrane for designing cell-free TXTL micro-reactors as efficient artificial cells.

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